Multiwalled carbon nanotubes enter broccoli cells enhancing growth and water uptake of plants exposed to salinity
© The Author(s) 2016
Received: 17 March 2016
Accepted: 24 May 2016
Published: 8 June 2016
Carbon nanotubes have been shown to improve the germination and growth of some plant species, extending the applicability of the emerging nano-biotechnology field to crop science.
In this work, exploitation of commercial multiwalled carbon nanotubes (MWCNTs) in control and 100 mM NaCl-treated broccoli was performed. Transmission electron microscopy demonstrated that MWCNTs can enter the cells in adult plants with higher accumulation under salt stress. Positive effect of MWCNTs on growth in NaCl-treated plants was consequence of increased water uptake, promoted by more-favourable energetic forces driving this process, and enhanced net assimilation of CO2. MWCNTs induced changes in the lipid composition, rigidity and permeability of the root plasma membranes relative to salt-stressed plants. Also, enhanced aquaporin transduction occurred, which improved water uptake and transport, alleviating the negative effects of salt stress.
Our work provides new evidences about the effect of MWCNTs on plasma membrane properties of the plant cell. The positive response to MWCNTs in broccoli plants opens novel perspectives for their technological uses in new agricultural practices, especially when 1plants are exposed to saline environments.
The positive effects of engineered nanomaterials on plants comprised increased germination percentage and rate; length of root and shoot, and vegetative biomass of seedlings with the involvement of distinct physiological processes related to the plant water balance, photosynthetic activity and nitrogen metabolism. Thus, the water status of many crops was affected by different nano-materials. It has been observed that coated seeds with nano-membranes may regulate the capacity of water imbibition when the seeds are ready to germination. Also, magnetic particles in seeds allowed the detection of moisture content during seed storage . Ag nanoparticles reduced the effects of microbial infection on gerbera flowers, increasing the water uptake and turgidity . TiO2 nanoparticles enhanced nitrate uptake in Soybean (Glycine max) plants, increasing the ability to absorb/use water, and promoting the antioxidant system. Also, TiO2 regulated water absorption in spinach seeds, with an increased germination rate . However, contrast results were found for the effect of engineered nanomaterials on plant water uptake and growth. Excess of metals nanoparticles resulted in toxic effects that involved a decrease of growth and abnormalities in cell division . Copper/copper oxide (Cu/Cu2O) nanoparticles may block water channels reducing water uptake .
Since their discovery in 1991 , carbon nanotubes (CNTs) have proven to be the most interesting of the nano-materials due to their unique mechanical, electrical, thermal and chemical properties . Their extraordinary physical properties give them potential uses in a multitude of fields; one that promises significant advances is biomedicine. In this area, they have been investigated for gene and drug delivery, diagnosis, tissue regeneration and implants. Therefore, most studies of CNTs have been related to tissues of humans and other animals , but investigation of their effects in plants is very scarce. Thus, the plant-CNTs interaction needs to be thoroughly investigated, from the molecular to the cellular and organ levels, integrating plant physiology to understand its complexity.
The first evidence of positive effects of multiwalled carbon nanotubes (MWCNTs) on crop plants was reported by Khodakovskaya et al. . Using a range of concentrations from 10 to 40 mg l−1, they observed that CNTs could penetrate the coats of tomato seeds, increasing germination rates and stimulating growth in young seedlings. In a more-recent study, Khodakovskaya et al.  demonstrated that MWCNTs, introduced into the soil through watering, can affect the phenotype of adult tomato plants. These plants produced a similar quantity of leaves but two-time more flowers and fruits than plants grown in regular soil. This observation opens new perspectives for the use of CNTs as growth regulators in conventional agricultural systems. Also, in Brassica juncea, the application of suitable CNTs concentration increased the heights of the roots , germination rate and growth .
However, some reports have indicated negative effects of CNTs on plants ; At high concentrations, the accumulation of graphene decreased the root growth of red spinach and cabbage  as consequence of massive electrolyte leakage, indicating an oxidation stress mechanism and damage in the plasma membrane that may affect water and solute transport . Fullerene was accumulated in the leaves following the symplastic route [16, 17] and the large aggregates accumulation within the vascular tissues may impede the appropriated translocation of water and nutrients to the aerial part . Tiwari et al. have shown that maize seedlings grown in agar reduced dramatically their growth and water uptake after treatment with different concentrations of pristine MWCNTs .
The effect of CNTs was dependent on the size, concentration and solubility of the applied CNTs. Hence, there is a need for further investigation before the application of CNTs can be considered as a widely-applicable means of increasing crop growth and productivity . In the study of the molecular mechanisms by which CNTs may act on plant physiology, a correlation between the activation of plant cell growth after MWCNTs exposure and the up-regulation of genes involved in cell division/cell wall formation and water transport, such as those controlling synthesis of aquaporins, was found . There are many reports indicating that aquaporins are crucial for root water uptake, seed germination, cell elongation, reproduction and photosynthesis . Also, the expression of a large number of aquaporin proteins has been shown to occur predominantly in roots and different experimental procedures have demonstrated, in various species, that aquaporins activity is linked to plant hydraulics during abiotic stress . However, it has been also demonstrated that MWCNTs may create new pores in the cell wall and plasma membrane allowing water transport to develop tomato and wheat seedlings [16, 17].
As it has been found that several genes involved in the general plant response to stress were up-regulated after carbon nanohorns treatment , conferring a positive response, the effect of CNTs in plants under stress deserves further attention.
The inhibition of plant growth by salinity via its effects at the physiological, biochemical and molecular levels has been studied widely [25, 26]. The homeostasis of ions and water is the main physiological process that plants need to optimise in order to maintain growth in saline environments [27, 28]. Osmotic adjustment may help plant cells to withstand salt stress, specifically to cope with the water deficit generated by the salt-induced osmotic imbalance, through the maintenance of the water potential gradient between the plant and the substrate, which is necessary to conserve water uptake and cell turgor for growth [29, 30]. Therefore, salinity is probably the most-suitable abiotic challenge under which to investigate the effect of CNTs, due to the similarity of the processes involved to those of other environmental stresses.
Membrane transport proteins and the surrounding lipids are crucial regulators of nutrient and water acquisition and of the exchanges of molecules between subcellular compartments; hence, they are vital to the maintenance of turgor under saline conditions . The trans-membrane water and solute fluxes are controlled by the abundance and activity of plasma membrane proteins . Also, the early response of proteins to salinity may be involved in the modulation of growth-regulating mechanisms and membrane stability . Also, changes in the chemical composition and physical properties of plasma membrane lipids have been observed as an adaptation to external salinity . A decrease in the unsaturation of fatty acids has been reported, together with an increase of sitosterol . In this sense, an increment in protein abundance in relation to the content of lipids in the plasma membrane was reported to play a role in the plasma membrane stability [36, 37]. In order to initiate further investigations at the intracellular level, the effect of MWCNTs on the plasma membrane should be elucidated. Therefore, in this work, we describe the results of applying commercial MWCNTs to control and salt-stressed (NaCl) broccoli plants in order to evaluate the effect of these synthetic CNTs on water and nutrient transport through the plasma membrane. The root hydraulic conductance, stomatal conductance, leaf water potential and CO2 fixation were measured as well as the mineral nutrient content, and the changes in the plasma membrane lipid composition were analysed and evaluated in relation to aquaporin abundance.
Plant material and growth conditions
Seeds of broccoli (Brassica oleracea L. var. Italica) were pre-hydrated with de-ionised water and aerated continuously for 12 h. After this, the seeds were germinated in vermiculite, in the dark at 28 °C, for 2 days. They were then transferred to a controlled-environmental chamber, with a 16-h light and 8-h dark cycle with temperatures of 25 and 20 °C and relative humidities of 60 and 80 %, respectively. Photosynthetically-active radiation (PAR) of 400 µmol m−2 s−1 was provided by a combination of fluorescent tubes (Philips TLD 36W/83, Jena, Germany and Sylvania F36W/GRO, Manchester, NH, USA) and metal halide lamps (Osram HQI, T 400W, Berlin, Germany). After 3 days, the seedlings were placed in 15 l containers with continuously-aerated Hoagland nutrient solution . After 1 week of growth, different treatments were applied for 7 days.
The Hoagland solution was used as the control. The MWCNTs were added to the control medium at concentrations of 10, 20, 40 and 60 mg l−1: Another set of plants were treated with concentrations of 80, 100 and 120 mM NaCl. Six plants per treatment were chosen for fresh weight (FW) determination. Plant FW was directly recorded with a portable balance (Sartorius CP224S). For further studies the combination of 100 mM NaCl + 10 mg l−1 MWCNT was chosen.
The second experimental set consisted of broccoli seedlings grown in Hoagland solution with NaCl (100 mM), with or without the simultaneous presence of 10 mg l−1 MWCNT. Six plants per treatment were chosen for FW determination. The total dry weight (DW) was measured after after drying the plant in an oven at 70 °C until constant weight.
Analysis of mineral elements
The concentrations of macronutrients (Ca, K, Mg, Na, P and S) were analysed in oven-dried samples of plant material (root and the third leaf), which had been ground finely in a mill grinder IKA model A10 (Staufen, Germany) to give particle sizes of 0.5–0.7 mm. The samples were digested in a microwave oven (CEM Mars Xpress, Mattheus, NC, USA) by HNO3–HClO4 (2:1) acid digestion. The elemental analysis was carried out using a Perkin–Elmer (Waltham, MA) 5500 model ICP emission spectrophotometer (Iris Intrepid II, Thermo Electron Corporation, Franklin, USA), at 589 nm and expressed as mg Kg−1 DW.
Leaf gas exchange parameters
Stomatal conductance (Gs) and net assimilation of CO2 (ACO2) were measured using a portable photosynthesis system (model LCA-4, ADC Bioscientific Ltd., Hoddesdon, UK) and a PLC-4N leaf chamber (11.35 cm2), configured to an open system. The third fully-expanded leaf was chosen for the analyses after the different treatments. Leaves were first equilibrated at a photon density flux of 400 μmol m−2 s−1 for at least 20 min. Gs and ACO2 were determined during the necessary seconds to stabilise the reading, once stabilised measurements were reordered every 10 s during 1 min. The measurements were made in the middle of the photoperiod in order to obtain the highest values. During all the measurements the cuvette temperature was 25 ± 2 °C, the CO2 concentration of the cuvette was 350 ± 5 ul l−1 and the leaf-to-air vapour pressure difference was 2.2 ± 0.3 kPa within the cuvette.
Root hydraulic conductance (L0)
Root hydraulic conductance (L0) was measured by pressurising the roots using a Schölander chamber. The aerial parts of the plants were removed, and the base of the stem was sealed with silicone grease into a tapered glass tube. The plant was then placed in the pressure chamber, with the same nutrient solution in which it had been grown, and a gradual increase of pressure (from 0.1 to 0.5 MPa) was applied to the roots, thereby generating a range of sap flows that represented whole-plant transpiration rates. Sap was collected in Eppendorf tubes and weighed on a precision balance. The sap flow, JV, was expressed in mg (g root FW)−1 h−1 and plotted against pressure (MPa), the slope being the L0 value [mg g (root FW)−1 h−1 MPa −1]. The measurements were made in the middle of the photoperiod, 1 week after applying the different treatments.
Treatment with sodium azide
Classically, sodium azide has been applied as an aquaporin functionality inhibitor ; its effect may be due to the fact that it inhibits protein phosphorylation and causes acidification of the cytoplasm, both effects contributing to the closure of aquaporin channels . Plants from each treatment were treated with sodium azide at a final concentration of 7 mM . Whole plants were immersed in their respective treatments and sodium azide (7 mM), so that the root system was kept undisturbed during the treatment. The plants were maintained under submersion for 60 min to allow uptake by the roots. Plants not treated with sodium azide were kept as a control.
Plasma membrane purification
Root plasma membranes were purified using the two-phase aqueous polymer technique described in Muries et al. . Fresh roots (20 g) were chopped into approximately 1 mm3 cubes and vacuum-infiltrated with 40 ml of a buffer containing 500 mM sucrose, 10 % glycerol, 20 mM Na2EDTA, 20 mM EGTA, 50 mM NaF, 5 mM glycerophosphate, 1 mM 1,10-phenantroline, 1 mM Na3VO4, 0.6 % PVP, 5 mM ascorbic acid, 5 mM DTT and 0.5 mg l−1 leupeptin in 50 mM Tris-MES, pH 8.0. After buffer infiltration, the roots were homogenised using a pestle and mortar and filtered through a nylon cloth (240 μm pores). The filtrate was centrifuged at 10,000g for 15 min. The supernatant was recovered and centrifuged at 55,000g for 35 min, yielding a microsomal pellet which was resuspended in 0.33 M sucrose, 2 mM DTT, 10 mM NaF and 5 mM phosphate buffer (pH 7.8). Plasma membranes were purified from microsomes by partitioning in a two-phase system mixture with a final composition of PEG-3350 (Sigma)/Dextran-T500 (GE Healthcare), 6.3 % (w/w) each in the presence of 5 mM KCl, 330 mM sucrose, 2.5 mM NaF and 5 mM potassium phosphate (pH 7.8) The two-phase system was centrifuged for 5 min at 4000g. The resulting upper phase, enriched in plasma membranes, was washed in 9 mM KCl, 300 mM sucrose, 0.2 M EDTA, 0.2 M EGTA, 0.5 M NaF and 10 mM Tris–borate, pH 8.3, and centrifuged at 55,000g for 35 min; the resulting lower phase was resuspended in 1 ml of 9 mM KCl, 300 mM sucrose, 0.2 M EDTA, 0.2 M EGTA, 0.5 M NaF, 2 mg l−1 leupeptin, 1 M DTT and 10 mM Tris–borate, pH 8.3.
Lipid analysis was carried out in the plasma membrane of theses purified vesicles whereas an enrichment in hydrophobic proteins was performed , previous the immunoblotting assay.
The protein concentration of the plasma membrane intrinsic protein (PIP)-enriched fraction was determined with the RC DC Protein Assay kit (BioRad), using BSA as standard. Plasma membrane samples were stored at −80 °C before use.
Gel electrophoresis and immunoblotting assay
Plasma membrane from the root tissues of broccoli plants was isolated as described previously. Protein (10 μg per lane) was loaded for 12 % sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE). The proteins had been denatured previously, by incubation at 56 °C for 20 min in the presence of 2 % (w/v) SDS and 100 mM DTT.
The proteins were transferred to a PVDF membrane and run for 20 min at 15 V, in an electrophoretic transfer cell (Trans-Blot SD cell, BioRad), using Towbin transfer buffer  with the addition of 0.05 % SDS. After this, the membrane was blocked for 1 h at room temperature, in tris-buffered saline (TBS) containing 2 % (w/v) skimmed dry milk. Then, the membrane was incubated for 1 h at room temperature in a buffer containing TBS with 0.05 % Tween 20, in the presence of an antibody (dilution 1:3000) raised against the first 42 N-terminus residues of Arabidopsis PIP1;1 (kindly provided by Prof. Dr. Anthony Schäffner) and another raised against a 17-amino-acid C-terminal peptide of Arabidopsis PIP2;2 (dilution 1:2000) (kindly provided by Dr. Veronique Santoni), shaking overnight at 4 °C. Goat anti-rabbit Immunoglobulin G (IgG) coupled to horseradish peroxidase was used as the secondary antibody (dilution 1:20,000). A chemiluminescent signal was developed using the West-Pico, Super Signal substrate (Pierce, Rockford, IL). The immunoblots were performed on samples from three independent experiments.
The intensity of each band was determined by a GS-800™ calibrated densitometer (Bio Rad, Barcelona, Spain). Background correction was performed by sampling membrane regions without spots and averaging their signals. The intensity of each band was estimated as the difference between the raw intensity of the protein of interest and the background. The scanned bands were normalised by calculating the ratio relative to the corresponding Coomassie-stained bands, thus ensuring that different intensities were not due to differences in the amount of protein loaded.
Leaf water potential (Ψω)
The leaf water potential (Ψω) of the third fully-expanded leaf was measured in the middle of the photoperiod using the pressure chamber technique .
Root plasma membrane lipid analysis
Sterol and fatty acids were determined as described by Mas et al.  and adapted by López-Perez et al.  in the root plasma membrane of broccoli plants. In an Eppendorf tube, a mixture of chloroform–methanol (1:2, 0.75 ml) was added to the membranes obtained (0.5 ml), along with b-cholestanol (20 μl, 0.1 mg ml−1)—used here as an internal standard for sterol analysis. Chloroform (CHCl3; 0.25 ml) was added and the mixture was shaken and centrifuged at 10,000g for 6 min. The CHCl3 layer was retained, evaporated to dryness under N2 (weighing this portion shows the amount of total lipids) and made up to 100 μl with CHCl3. For sterol analysis, 20 μl of the CHCl3 extract were placed in a glass vial (2 ml), evaporated to dryness under N2 and acetylated using pyridine (50 μl) and Ac2O (100 μl). After 2 h, the solvents were evaporated under N2, ethyl acetate (20 μl) was added and the sterol was analysed by gas chromatography (GC) using an HP5-bonded capillary column (30 m × 0.25 mm × 0.25 μm) coupled to a flame ionisation detector (FID), with H2 as carrier (1 ml min−1) and a temperature programme of 120–260 °C at 5 °C min−1, then 260–280 °C at 2 °C min−1 and finally 280–300 °C at 6 °C min−1. The injector and detector temperatures were 150 and 320 °C, respectively. Bound fatty acids were determined in 20–25 μl portions of the CHCl3 extract, by evaporating them to dryness under N2, transmethylating with sodium methoxide (0.5 N) in methanol (0.5 ml) and heating at 30 °C for 7 min. The resultant fatty acid methyl esters were extracted with hexane (1 ml), evaporated under N2, dissolved in ethyl acetate (20 μl) and analysed by GC using an HP5-bonded capillary column (30 m × 0.25 mm × 0.25 μm), with FID, He as carrier (1 ml min−1) and a temperature programme of 150–195 °C at 3 °C min−1, then 195–220 °C at 2 °C min−1 and finally 220–300 °C at 6 °C min−1. The injector and detector temperatures were 280 and 300 °C, respectively.
Lipid/protein ratio in the plasma membrane
The total lipids were determined by weighing the lipid extraction phase for lipid analysis, after evaporation to dryness under N2. The protein concentration of the plasma-membrane-enriched fraction was determined as described before.
Transmission electron microscopy
Root (8–10 cm from the tip), stem (3 cm from the base) and leaf (third leaf) samples were collected and then cut into small pieces (1–2 mm) and immersed in 2.5 % (v/v) glutaraldehyde and 3 % paraformaldehyde in 0.1 m sodium phosphate buffer (pH 7.2) for 2.5 h. After three 15 min washes with the buffer, the samples were postfixed in 1 % osmium tetroxide, in the same buffer, for 2 h. After this, three washes with phosphate buffer were performed. All fixed tissues were dehydrated in a graded series of ethanol (35, 50, 70, 96 and 100 %), then infiltrated, first with a propylene oxide and then with propylene oxide and Spurr’s resin mixture. The samples were then immersed in Spurr’s resin overnight at 4 °C. Finally, the samples were embedded in Spurr resin. Blocks were sectioned on a Leica EM UC6 ultramicrotome, collected on Formvar-coated copper grids and stained with uranyl acetate followed by lead citrate. Sections were examined using a Philips Tecnai 12 transmission electron microscope. For each treatment, an average of six samples from four different tissues was investigated. For each sample, 5–10 ultrathin sections were examined.
Statistical analyses were performed using SPSS Release 18 for Windows. Significant differences between the values of all parameters were determined at P ≤ 0.05, according to Tukey’s test.
The fresh weight (FW) of the whole plants was determined after 7 days of growth at different concentrations of the MWCNTs (10, 20, 40, 60 mg l−1) (Additional file 1). There was a FW decrease at 20, 40 and 60 mg l−1 MWCNT, compared to the control value, while 10 mg l−1 MWCNTs produced a significant increase (32.75 %).
Effect of MWCNTs on fresh weight under salt stress
Ca, K, Na, P, S and Mg (10−4 mg kg−1DW) levels in the root and shoot of control broccoli plants and plants treated with 10 mg l−1 MWCNTs, 100 mM NaCl and 100 mM NaCl + 0.10 mg l−1 MWCNTs
2.30 ± 0.10 a
4.61 ± 0.30 a
0.12 ± 0.03 c
1.88 ± 0.10 a
0.65 ± 0.07 a
0.95 ± 0.07 a
2.07 ± 0.11 a
4.75 ± 0.51 a
0.11 ± 0.02 c
1.66 ± 0.12 a
0.71 ± 0.07 a
0.83 ± 0.07 a
0.99 ± 0.04 b
3.46 ± 0.42 b
2.02 ± 0.18 b
1.05 ± 0.10 b
0.58 ± 0.06 a
0.62 ± 0.05 b
NaCl + MWCNT
0.70 ± 0.03 b
3.25 ± 0.29 b
2.34 ± 0.10 a
0.82 ± 0.08 b
0.63 ± 0.05 a
0.69 ± 0.04 b
2.10 ± 0.11 a
4.57 ± 0.43 a
0.13 ± 0.05 c
0.54 ± 0.05 a
0.71 ± 0.06 ab
0.38 ± 0.04 a
2.48 ± 0.18 a
4.51 ± 0.27 a
0.09 ± 0.02 c
0.54 ± 0.03 a
0.96 ± 0.07 a
0.43 ± 0.03 a
1.27 ± 0.17 b
2.36 ± 0.10 c
2.26 ± 0.28 b
0.46 ± 0.07 a
0.61 ± 0.06 b
0.33 ± 0.03 a
NaCl + MWCNT
1.34 ± 0.10 b
3.27 ± 0.12 b
3.11 ± 0.12 a
0.55 ± 0.05 a
0.59 ± 0.04 b
0.30 ± 0.03 a
Stomatal conductance and net assimilation of CO2
Net assimilation of CO2 (ACO2) was measured on the same days as Gs, but only the final values are shown since they are representative of every day (Fig. 3b). Only plants treated with NaCl showed significant decreases of ACO2. The other treatments did not affect ACO2—which remained unchanged from the first day of measurement.
Root hydraulic conductance
When plants were treated with sodium azide, L0 was lower. Control and MWCNTs-treated plants showed similar reductions of L0 (56.47 and 53.26 %, respectively) after sodium azide treatment. The NaCl and NaCl + MWCNTs-treated plants exhibited very-low L0 values that were further affected by sodium azide treatment, but again plants exposed to NaCl + MWCNTs showed higher values than NaCl-treated plants.
Aquaporin protein abundance
For quantification of broccoli PIP1 and PIP2 protein abundance in the roots, Western blotting was performed. A unique band at 29 kDa (monomeric form) was detected with both aquaporin (PIP1 and PIP2) antibodies, in all the samples analysed. No dimeric bands were detected (Fig. 4b). The immunostaining intensity differed among treatments and depended on the PIP subfamily. Thus, similar PIP1 abundance was found in control and NaCl-treated plants, while a significant increase in the PIP1 content due to the MWCNTs treatment was observed under both non-saline and saline conditions. However, PIP2 proteins were increased by both the NaCl and MWCNTs treatments, with respect to the control, but the increment was higher with MWCNTs application. The PIP2 abundance was the highest when the combination of NaCl and MWCNTs was applied.
Leaf water potential
Leaf water potential (ψw) (MPa) of control broccoli plants and plants treated with 10 mg l−1 MWCNTs, 100 mM NaCl and 100 mM NaCl + 0.10 mg l−1 MWCNTs
−0.30 ± 0.03a
−0.25 ± 0.04a
−0.73 ± 0.08c
NaCl + MWCNTs
−0.55 ± 0.08b
Effect on the root plasma membrane lipid composition
Effect of MWCNT on changes in the lipid composition of the plasma membrane of roots of broccoli plants grown for 7 days with distinct treatments
NaCl + MWCNTs
137.5 ± 5.53 a
151.8 ± 4.14 c
143.6 ± 4.41 b
153.4 ± 2.45 c
0.75 ± 0.08 a
1.68 ± 0.01 b
0.95 ± 0.09 a
1.78 ± 0.12 b
0.21 ± 0.01 b
0.09 ± 0.01 a
0.63 ± 0.07 b
0.08 ± 0.08 a
1.25 ± 0.04 a
1.96 ± 0.09 b
1.38 ± 0.11 a
1.82 ± 0.046 b
The effect of different treatments on the free sterol concentration of the root plasma membrane was also investigated. The sitosterol concentration was higher in both MWCNTs and NaCl + MWCNTs-treated plants, resulting in very-low stigmasterol/sitosterol ratio. However, NaCl-treated plants showed a higher stigmasterol/sitosterol ratio, due to a decreased sitosterol concentration. The protein/lipid ratio in the root plasma membrane was enhanced by all the treatments, relative to the control, the increase being slightly higher in the two treatments with MWCNTs.
Subcellular distribution of MWCNTs
It has been previously demonstrated that MWCNTs can penetrate seed coats and promote germination and growth [9, 48, 49]. It has been observed that CNTs may promote water uptake as a growth stimulator [12, 50] with an increased expression of PIP1 genes in “in vitro” tobacco cell cultures . However, the effect of MWCNTs on the plasma membrane properties and its ability to transport water under saline- stress conditions has not been studied. Controversial results of beneficial or toxic implications of MWCNTs on plant growth has been reported , and different observations depended mainly on the plant genotype, plant growth medium, environmental conditions, type of MWCNTs, their size, concentration and chemical surface functionalization .
Our transmission electron microscopy (TEM) analysis determined that 75 % of the nanotubes had 0.1–0.5 μm length in spite those manufacturer specifications (0.5–10 μm length). This size after ultrasonication to disperse MWCNTs in the aqueous solution and the high-purity of MWCNTs used (95 %) had a positive effect on the growth of broccoli plants at the seedling stage under both, saline and non-saline conditions.
The application of the treatments was performed in adult plants when they were assumed to have a mineral-nutrient status consistent with optimum growth and the plants were grown in a hydroponic medium to allow the MWCNTs to enter the roots by more-direct penetration.
Studies of transport and translocation of nanotubes assume that there is no interaction with the substances present on the root surface in order to allow CNTs adsorption . Thus, penetration could be taken place through the apoplastic pathway by capillarity until arrive at a narrower passage than their size, being then accumulated with impediment of nutrient transport. However, in our broccoli plants the MWCNTs diameter and length and their concentration in the media were not limiting factors for the nutrient uptake availability of the plant. As previously done by Begun and Fugetsu  for spinach, the MWCNTs were applied to a Hoagland nutrient solution, but at lower concentrations. These authors applied a range of MWCNTs concentrations from 125 to 1000 mg l−1, with no positive effects on plant growth. For our broccoli plants an interval from 10 to 60 mg l−1 was used: 10 mg l−1 MWCNTs gave a significant increase of growth but the rest of the concentrations produced perturbations. Improved growth due to MWCNTs application was related to increases in the nutrient and water uptake in maize cell cultured plants . The authors considered the action of opposing forces, the CNTs ion-transient-dipole interaction, that retain ions in the roots and promote the water flow that facilitates further ion uptake. Therefore, an optimum concentration of MWCNTs was related to the effect of these opposing forces. In our broccoli roots, MWCNTs originated an increase in the Na concentration relative to NaCl-treated plants, but the rest of tissue nutrient concentrations were not altered by any of the treatments. Our results are in agreement with those reported by Husen and Siddiqi , where essential plant nutrients were absorbed by the plant in the presence of nanomaterials suspended in aqueous media. However, variations between our results and those of Tiwari et al. , who observed differences for most of nutrients, could be related to the type of growth medium—nutrient agar gel vs. nutrient solution, the aqueous dispersion of the MWCNTs being greater in the latter—and to the experimental entity, maize seedlings vs. adult broccoli plants, affecting the root content of the most abundant cation, Na, in the nutrient solution. Root Na rise could be also the consequence of increased water uptake that was more efficient in MWCNTs-treated plants, which may be related directly to their greater growth.
Broccoli plants are moderately salt tolerant and, therefore, can cope with low external salinity, with only a slight decrease in growth . In our work, the NaCl concentration (100 mM) was higher than the maximum assayed in previous studies (80 mM), being based on the level at which growth decreased during a limited experimental exposure time. Thus, in previous report, we observed a biphasic growth inhibition of broccoli plants in response to salinity and during the second phase the internal injury was due to accumulation of salts in transpiring leaves . In this work, similar K/Na ratios were observed in the shoots of NaCl and NaCl + MWCNTs-treated plants. Thus, the maintenance of a high K/Na ratio for salt tolerance was not the operative mechanism of MWCNTs.
Salinity in broccoli plants was also related to alterations of the membrane lipid composition and fluidity—that contribute to reductions of cell expansion . This response was related to water uptake and transport—regulated by aquaporins functionality and abundance, key factors in the movement of water into the plant. The present work investigated whether or not the MWCNTs interfere with the response of broccoli plants to salinity, since they have been reported to target membranes and aquaporins. The application of MWCNTs increased plant growth, the increment being higher in NaCl-treated plants, and the amelioration of the salinity effect was very apparent after 7 days of MWCNTs treatment. In control and NaCl-treated plants supplied with MWCNTs, the greater presence of PIP1 and PIP2 aquaporins corroborated the increase in water passage through the plasma membrane that was related to higher L0. The stimulation of aquaporins production in in vitro tomato plants by MWCNT has been reported  as the main factor inducing growth, but other genes involved in cell division have been activated also  and cannot be ruled out in our broccoli plants.
It has been widely reported that salinity decreases stomatal conductance (Gs) and CO2 fixation . In broccoli plants, these results have been related to both stomatal aperture and photosynthetic rate or net CO2 assimilation (ACO2) ; stomatal closure resulted in a decrease in leaf transpiration and leaf internal CO2 concentration. Also, it has been reported that plant cell homeostasis in NaCl-treated plants must involve the combined regulation of L0 and Gs, with a consequent dependence on root aquaporins . In our plants, MWCNTs slightly increased Gs and ACO2, even in the NaCl treatment, and a correlation between stomatal behaviour and L0 was observed under non-saline and saline conditions. Therefore, the simultaneous rises in Gs and L0 induced by MWCNTs may indicate enhanced symplastic movement of water, through an increased abundance of aquaporins, which maintained the cellular water balance, ψw and, in turn, augmented plant growth. Under saline conditions, the increment in L0 and ψw could have been related, in addition to the greater aquaporin abundance, to higher aquaporin functionality, as deduced from the sodium azide experiments. In previous work, HgCl2, a mercurial inhibitor of aquaporin functionality, was used; the reversal of its effect by DTT was used to demonstrate the absence of side effects . Also, K+ leakage was used as a control . Mercurials act through covalent union with cysteine residues of aquaporin proteins, within the water pore and in other regions of the protein, causing either blockage or conformational changes that lead to inhibition of water transport . Thus, the use of alternative compounds such as azide, that inhibits protein phosphorylation and causes acidification of the cytoplasm, hence contributing to closure of the aquaporin channel , has been very useful due to the absence of side effects . The azide results may demonstrate the involvement of the symplastic route of water movement in the NaCl + MWCNTs-treated plants with higher L0 reductions than control plants. But the results must be carefully interpreted since mutagenic effect of sodium azide on growth and yield traits of Eruca sativa (L.), another Brassicaceae, has been observed when the compound was applied at a concentration of 3 mM .
Carbon nanotubes can be taken up by roots and moved to the leaves . Although interaction with mineral nutrients has not been claimed to be the driving force for apoplastic transport of MWCNTs, the driving force of water should allow their movement through the plant . Also, their penetration through the cell wall and membranes has been observed only on some occasions, when the concentration of the nanotubes applied was high (100–1000 mg l−1) . However, this not the case of our broccoli plants and MWCNTs pass through the cell wall in the plant mature stage and they were observed in intercellular spaces, vacuole, plasma membrane and cytoplasm in the cortical cells of the roots and stem in control and NaCl-treated plants. This could be related to the size and low concentration used (10 mg l−1) to the rate of movement through the symplastic/apoplastic pathway—that allowed MWCNT passively diffused across the cells. Also MWCNTs distribution in broccoli plants organelles was influenced by their size, high resolution transmission electron microscopy showed that long MWCNTs (larger than 200 nm) were concentrated in subcellular organelles while the shorter ones (30–100 nm) were acquired into vacuoles, nucleus and plastids [59, 60]. Similarly, Chen et al.  demonstrated that the MWCNTs could be translocated from the roots to the upper organs within mustard mature plants under the transpiration stream. However, in our broccoli plants MWCNTs were not found in the leaves of any plants. A diffusion and leakage of MWCNTs in the aerial part must be not discarded as it was observed for SWCNTs when the size of particle is too small [59, 62]. By contrast, higher accumulations were observed in NaCl + MWCNTs-treated plants with lower Gs values that MWCNTs-treated plants. Thus, MWCNTs accumulation should be investigated in terms of the action driven by the root water pressure.
Also, changes in the plasma membrane composition could be very important in relation to MWCNTs penetration within our broccoli plants. Although it has been pointed out that CNTs penetrate cells directly rather than through endocytosis  and that they can act as molecular transporters in walled cells , their passage through membranes seems to be related to the membrane stability and to lipid trapping by lipid exchange . Therefore, the changes in control lipid composition in our membranes were a response to the MWCNTs and salinity. The sitosterol/stigmasterol ratio was increased in the plasma membranes of plants exposed to salinity, indicating a swift increase in water permeability, since sitosterol has been found to be very efficient in regulating water permeability and salt protection [65, 66]. However, the ratio was strongly decreased by the MWCNTs, which have been reported to give rise to more-stable membranes in the raft domains . This effect should be investigated; it could form part of a mechanism to compensate for greater water movement through the increased number of aquaporin proteins.
The increase in the DBI and RUFA of the fatty acid content in the leaf plasma membrane of NaCl-treated plants has been reported to be related to reductions in membrane fluidity . But, these changes reduce fluidity, increasing water permeability . The increments in DBI and RUFA in our root plasma membrane as a consequence of the application of MWCNTs were higher than those induced by salinity; therefore, these carbon compounds produced more rigidity but probably also increased membrane permeability, relative to salt stress.
Recently, it has been shown that plasma membrane lipid modifications in broccoli plants in response to salinity occurred in order to maintain protein function and ensure membrane permeability . Also, the increased content of proteins, such as aquaporins, is relevant with regard to promotion of ion and water transport and maintenance of the electrostatic gradient across the plasma membrane, and hence cell homeostasis, but also for decreasing damage to the membrane and ensuring its stability . Nevertheless, the observation that biological membranes are able to form ordered lipid domains (raft domains) that are highly stable  and enriched in aquaporins , but with unknown function, reinforces the idea that the variability of plasma membrane composition and fluidity, as a response to salinity and MWCNTs, may be the key to understanding their physiological effects.
The results presented in this work reinforce and build upon previous results obtained with the application of CNTs to plants cultured in vitro, extending the approach to adult plants. Also, the novel use of salt-stressed plants has shown that the MWCNTs influenced the primary plant response in relation to water and nutrient uptake. The positive biochemical changes found could simply have been due to the known physical changes produced in cells and tissues by the MWCNTs and under salt stress these compounds may retain Na ions in the root that promote water uptake. The plants appeared able to cope with changes in the water gradient through the imposed symplastic pathway, giving positive results. But, these events are only the starting point of a chain of biochemical changes that should be investigated as well as the movement of MWCNTs to edible part of the plants (e.g: leaves and fruits) and the environmental implications. In conclusion, the positive growth response by the broccoli plants to low concentrations of MWCNTs opens up new perspectives for the use of MWCNTs in agriculture, especially when plants are growing under stress.
MCMB, LZ and NC conducted the experimental work. MCMB and MC wrote the manuscript. MC contributed reagents/materials/analysis tools and gave advices to perform the needed experiments. All authors read and approved the final manuscript.
The authors thank Dr. D. Walker, for correction of the written English in the manuscript. This work was funded by the Spanish Ministerio de Economía y Competitividad (AGL2012-40175-C02-01). Najla Chalbi was supported by a doctoral fellowship from the Tunisian Ministry of Higher Education and Scientific Research (MHESR).
The authors declare that they have no competing interests.
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- Chinnamuthu CR, Boopathi PM. Nanotechnology and agroecosystem. Madras Agric J. 2009;96:17–31.Google Scholar
- Nair R, Varghese SH, Nair BG, Yoshida MY, Kumar DS. Nanoparticle material delivery to plants. Plant Sci. 2010;179:154–63.View ArticleGoogle Scholar
- Zheng L, Hong F, Lu S, Liu C. Effect of nano-TiO2 on strength of naturally aged seeds and growth of spinach. Biol Trace Elem Res. 2005;104:83–91.View ArticleGoogle Scholar
- Niederberger M. Nonaqueous sol-gel routes to metal oxide nanoparticles. Acc Chem Res. 2007;40:793–800.View ArticleGoogle Scholar
- Geremias R, Fattorini D, F´avere VTD, Pedrosa RC. Bioaccumulation and toxic effects of copper in common onion Allium cepa L. Chem Ecol. 2010;26:19–26.View ArticleGoogle Scholar
- Iijima S. Helical microtubules of graphitic carbon. Nature. 1991;354:56–8.View ArticleGoogle Scholar
- Dresselhaus MS, Dresselhaus G, Jorio A. Unusual properties and structure of carbon nano tubes. Annu Rev Mater Res. 2004;34:247–78.View ArticleGoogle Scholar
- Eatermadi A, Darae H, Karimkhanloo H, Koui M, Zarghami N, Akbarzadeh A, et al. Carbon nanotubes: properties, synthesis, purification, and applications. Nanoscale Res Lett. 2014;9:393.View ArticleGoogle Scholar
- Khodakovskaya M, Dervishi E, Mahmood M, Xu Y, Li Z, Watanabe F, et al. Carbon nanotubes are able to penetrate plant seed coat and dramatically affect seed germination and plant growth. ACS Nano. 2009;3:3221–7.View ArticleGoogle Scholar
- Khodakovskaya M, Kim B, Kim J, Alimohammdi M, Dervishi E, Mustafa T, et al. Carbon nanotubes as plant growth regulators: effects on tomato growth, reproductive system, and soil microbial community. Small. 2013;9:115–23.View ArticleGoogle Scholar
- Ghodake G, Seo YD, Park D, Lee DS. Phytotoxicity of carbon nanotubes assessed by Brassica juncea and Phaseolus mungo. J Nanoelectron Optoe. 2010;5:157–60.View ArticleGoogle Scholar
- Mondal A, Basu R, Das S, Nandy P. Beneficial role of carbon nanotubes on mustard plant growth: an agricultural prospect. J Nanopart Res. 2011;13:4519–28.View ArticleGoogle Scholar
- Safiuddin M, Gonzalez M, Cao JW, Tighe SL. State of-the-art report on use of nano-materials in concrete. Int J Pavement Eng. 2014;15:940.View ArticleGoogle Scholar
- Begum P, Ikhtiari R, Fugetsu B. Graphene phytotoxicity in the seedling stage of cabbage, tomato, red spinach, and lettuce. Carbon. 2011;49:3907–19.View ArticleGoogle Scholar
- Fugetsu B, Parvin B. Graphene phytotoxicity in the seedling stage of cabbage, tomato, red spinach, and lettuce. In: Bianco S, editor. Carbon nanotubes-from research to applications. CC BY-NC-SA. 2011.Google Scholar
- Liu Q, Zhao Y, Wan Y, Zheng J, Zhang X, Wang C, et al. Study of the inhibitory effect of water-soluble fullerenes on plant growth at the cellular level. ACS Nano. 2010;4:5743–8.View ArticleGoogle Scholar
- Gao J, Wang Y, Folta KM, Krishna V, Bai W, Indeglia P, et al. Polyhydroxy fullerenes (fullerols or fullerenols): beneficial effects on growth and lifespan in diverse biological models. PLoS One. 2011;6(5):e19976.View ArticleGoogle Scholar
- Lin S, Reppert J, Hu Q, Hudson JS, Reid ML, Ratnikova TA, et al. Uptake, translocation, and transmission of carbon nanomaterials in rice plants. Small. 2009;5:1128–32.View ArticleGoogle Scholar
- Tiwari DK, Dasgupta-Schubert N, Villaseñor Cendejas N, Villegas J, Carreto Montoya L, García SEB. Interfacing carbon nanotubes (CNT) with plants: enhancement of growth, water and ionic nutrient uptake in maize (Zea mays) and implications for nanoagriculture. Appl Nanosci. 2014;4:577–91.View ArticleGoogle Scholar
- Husen A. Siddiqi K Carbon and fullerene nanomaterials in plant system. J Nanobiotechnol. 2014;12:16.View ArticleGoogle Scholar
- Khodakovskaya M, Silva K, Biris A, Dervishi E, Villagarcia H. Carbon nanotubes induce growth enhancement of tobacco cells. ACS Nano. 2012;6:2128–35.View ArticleGoogle Scholar
- Maurel C. Plant aquaporins: novel functions and regulation properties. FEBS Lett. 2007;581:2227–36.View ArticleGoogle Scholar
- Martínez-Ballesta MC, Rodríguez-Hernández MC, Alcaraz-López C, Mota-Cadenas C, Muries B, Carvajal M. Plant hydraulic conductivity: The aquaporins contribution. In: Elango L, editor. Hydraulic conductivity—issues, determination and applications. Rijeka: In Tech; 2011. p. 103–21. ISBN 978-953-307-288-3.Google Scholar
- Lahiani MH, Dervishi E, Chen JH, Nima Z, Gaume A, Biris AS, et al. Impact of carbon nanotube exposure to seeds of valuable crops. ACS Appl Mater Interfaces. 2013;5:7965–73.View ArticleGoogle Scholar
- Winicov I. New molecular approaches to improving salt tolerance in crop plants. Ann Bot. 1998;82:703–10.View ArticleGoogle Scholar
- Munns R. Comparative physiology of salt and water stress. Plant Cell Environ. 2002;25:239–50.View ArticleGoogle Scholar
- Munns R, Tester M. Mechanisms of salinity tolerance. Annu Rev Plant Biol. 2008;59:651–81.View ArticleGoogle Scholar
- Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ. Plant cellular and molecular responses to high salinity. Annu Rev Plant Physiol Plant Mol Biol. 2000;51:463–99.View ArticleGoogle Scholar
- Carvajal M, Martinez V, Alcaraz CF. Physiological function of water channels is affected by salinity in roots of paprika pepper. Physiol Plantarum. 1999;105:95–101.View ArticleGoogle Scholar
- Carvajal M, Cerdá A, Martínez V. Does calcium ameliorate the negative effect of NaCl on melon root water transport by regulating water channel activity? New Phytol. 2000;145:439–47.View ArticleGoogle Scholar
- López-Perez L, Martinez-Ballesta MC, Maurel C, Carvajal M. Changes in plasma membrane lipids, aquaporins and proton pump of broccoli roots, as an adaptation mechanism to salinity. Phytochemistry. 2009;70:492–500.View ArticleGoogle Scholar
- Chrispeels MJ, Crawford NM, Schroeder JI. Proteins for transport of water and mineral nutrients across the membranes of plant cells. Plant Cell. 1999;11:661–75.View ArticleGoogle Scholar
- Witzel K, Matros A, Strickert M, Kaspar S, Peukert M, Mühling KH, et al. Salinity stress in roots of contrasting barley genotypes reveals time-distinct and genotype-specific patterns for defined proteins. Mol Plant. 2014;7:336–55.View ArticleGoogle Scholar
- Elkahoui S, Smaoui A, Zarrouk M, Ghrir R, Limam F. Salt-induced lipid changes in Catharanthus roseus cultured cell suspension. Phytochemistry. 2004;65:1911–7.View ArticleGoogle Scholar
- Bohn M, Lüthje S, Sperling P, Heinz E, Dörffling K. Plasma membrane lipid alterations induced by cold acclimation and abscisic acid treatment of winter wheat seedlings differing in frost resistance. J Plant Physiol. 2007;164:146–56.View ArticleGoogle Scholar
- Chalbi N, Martinez-Ballesta MC, Youssef NB, Carvajal M. Intrinsic stability of Brassicaceae plasma membrane in relation to changes in proteins and lipids as a response to salinity. J Plant Physiol. 2015;175:148–56.View ArticleGoogle Scholar
- Sreedharan S, Shekhawat UK, Ganapathi TR. Constitutive and stress-inducible overexpression of a native aquaporin gene (MusaPIP2;6) in transgenic banana plants signal its pivotal role in salt tolerance. Plant Mol Biol. 2015;88:41–52.View ArticleGoogle Scholar
- Epstein E. Mineral nutrition of plants: principles and perspectives. New York: Wiley; 1972.Google Scholar
- Fitzpatrick KL, Reid RJ. The involvement of aquaglyceroporins in transport of boron in barley roots. Plant Cell Environ. 2009;32:1357–65.View ArticleGoogle Scholar
- Tournaire-Roux C, Sutka M, Javot H, Gout E, Gerbeau P, Luu DT, et al. Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins. Nature. 2003;425:393–7.View ArticleGoogle Scholar
- Bárzana G, Aroca R, Chaumont F, Martínez-Ballesta MC, Carvajal M, Ruiz-Lozano JM. The arbuscular mycorrhizal symbiosis increases apoplastic water flow in roots of the host plant under both well-watered and drought stress conditions. Ann Bot. 2012;109:1009–17.View ArticleGoogle Scholar
- Muries B, Faize M, Carvajal M, Martínez-Ballesta MC. Identification and differential induction of the expression of aquaporins by salinity in broccoli plants. Mol BioSyst. 2011;7:1322–35.View ArticleGoogle Scholar
- Santoni V, Vinh J, Pflieger D, Sommerer N, Maurel C. A proteomic study reveals novel insights into the diversity of aquaporin forms expressed in the plasma membrane of plant roots. Biochem J. 2003;373:289–96.View ArticleGoogle Scholar
- Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA. 1979;76:4350–4.View ArticleGoogle Scholar
- Turner NC. Measurement of plant water status by the pressure chamber technique. Irrig Sci USA. 1988;9:289–308.View ArticleGoogle Scholar
- Mas A, Navarro-Pedreño J, Cooke DT, James CS. Characterization and lipid composition of the plasma membrane in grape leaves. Phytochemistry. 1994;35:1249–53.View ArticleGoogle Scholar
- López-Berenguer C, García-Viguera C, Carvajal M. Are root hydraulic conductivity responses to salinity controlled by aquaporins in broccoli plants? Plant Soil. 2006;279:13–23.View ArticleGoogle Scholar
- Villagarcia H, Dervshi E, De Silva K, Biris A, Khodakovskaya M. Surface chemistry of carbon nanotubes impacts the growth and expression of water channel protein in tomato plants. Small. 2012;8:2328–34.View ArticleGoogle Scholar
- Yan S, Zhao L, Li H, Zhang Q, Tan J, Huang M, et al. Single-walled carbon nanotubes selectively influence maize root tissue development accompanied by the change in the related gene expression. J Hazard Mat. 2013;246–247:110–8.View ArticleGoogle Scholar
- Tripathi S, Sonkar SK, Sarkar S. Growth stimulation of gram (Cicer arietinum) plant by water soluble carbon nanotubes. Nanoscale. 2011;3:1176.View ArticleGoogle Scholar
- Begum P, Fugetsu B. Phytotoxicity of multi-walled carbon nanotubes on red spinach (Amaranthus tricolor L.) and the role ascorbic acid as an antioxidant. J Hazard Mater. 2012;243:212–22.View ArticleGoogle Scholar
- Sidiqui MH, Al-Whaibi MH, Firoz M, Al-Khaishany MY. Role of nanoparticles in plants. In: Sidiqui MH, Al-Whaibi MH, Firoz M, editors. Nanotechnology and plant sciences. Springer; 2015. p. 19–35. doi:10.1007/978-3-319-14502-0_2.
- Zaghdoud C, Mota-Cadenas C, Carvajal M, Muries B, Ferchichi A, Martínez-Ballesta MC. Elevated CO2 alleviates negative effects of salinity on broccoli (Brassica oleracea L. var Italica) plants by modulating water balance through aquaporins abundance. Environ Exp Bot. 2013;95:12–24.View ArticleGoogle Scholar
- Martinez-Ballesta MC, Diaz R, Martinez V, Carvajal M. Different blocking effect of HgCl2 and NaCl on aquaporins of pepper plants. J Plant Physiol. 2003;160:1487–92.View ArticleGoogle Scholar
- Carvajal M, Cooke DT, Clarkson DT. High temperature effects on hydraulic conductance and plasma membrane fluidity of nutrient deprived wheat roots. Plant Cell Environ. 1996;19:1110–4.View ArticleGoogle Scholar
- Niemietz CM, Tyerman SD. New potent inhibitors of aquaporins: silver and gold compounds inhibit aquaporins of plant and human origin. FEBS Lett. 2002;531:443–7.View ArticleGoogle Scholar
- Al-Qurainy F. Effects of sodium azide on growth and yield traits of Eruca sativa (L.). World Appl Sci J. 2009;7:220–6.Google Scholar
- Smirnova E, Gustev A, Zayteseva O, Sheina O, Tkachev A, Kuznesova E, et al. Uptake and accumulation of multiwalled carbon nanotubes change the morphometric and biochemical characteristics of Onobrychis arenaria seedlings. Front Chem Sci Eng. 2012;6:132–8.View ArticleGoogle Scholar
- Liu Q, Chen B, Wang Q, Shi X, Xiao Z, Lin J, Fang X. Carbon nanotubes as molecular transporters for walled plant cells. Nano Lett. 2009;9:1007–10.View ArticleGoogle Scholar
- Serag MF, Kaji N, Habuchi S, Bianco A, Baba Y. Nanobiotechnology meets plant cell biology: carbon nanotubes as organelle targeting nanocarriers. RSC Adv. 2013;3:4856–62.View ArticleGoogle Scholar
- Chen G, Qiu J, Liu Y, Jiang R, Cai S, Liu Y, et al. Carbon nanotubes act as contaminant carriers and translocate within plants. Sci Rep. 2015;5:15682.View ArticleGoogle Scholar
- Serag MF, Braeckmans K, Habuchi S, Kaji N, Bianco A, Baba Y. Spatio temporal visualization of subcellular dynamics of carbon nanotubes. Nano Lett. 2012;12:6145–51.View ArticleGoogle Scholar
- Serag MF, Kaji N, Gaillard C, Okamoto Y, Terasaka K, Jabasini M, et al. Trafficking and subcellular localization of multiwalled carbon nanotubes in plant cells. ACS Nano. 2011;5:493–9.View ArticleGoogle Scholar
- Giraldo JP, Landry MP, Faltermeier SM, McNicholas TP, Iverson NM, Boghossian AA, et al. Plant nanobionics approach to augment photosynthesis and biochemical sensing. Nat Mater. 2014;13:400–8.View ArticleGoogle Scholar
- Silva C, Aranda FJ, Ortiz A, Carvajal M, Martínez V, Teruel JA. Root plasma membrane lipid changes in relation to water transport in pepper: a response to NaCl and CaCl2 treatment. Plant Biol. 2007;50:650–7.View ArticleGoogle Scholar
- Basyuni M, Baba S, Kinjo Y, Oku H. Salinity increases the triterpenoid content of a salt secretor and a non salt secretor mangrove. Aquat Bot. 2012;97:17–23.View ArticleGoogle Scholar
- Ryaz AB, Panstruga R. Lipid rafts in plants. Planta. 2005;223:5–19.View ArticleGoogle Scholar
- Guimaraes FVA, Lacerda CF, Marques EC, Miranda MRA, Abreu CEB, Prisco JT, et al. Calcium can moderate changes on membrane structure and lipid composition in cowpea plants under salt stress. Plant Growth Reg. 2011;65:55–63.View ArticleGoogle Scholar
- Levental I, Grzybek M, Simons K. Raft domains of variable properties and compositions in plasma membrane vesicles. Proc Natl Acad Sci USA. 2011;108:11411–6.View ArticleGoogle Scholar
- Chevalier AS, Chaumont F. Trafficking of plant plasma membrane aquaporins: multiple regulation levels and complex sorting signals. Plant Cell Physiol. 2014;56:819–29.View ArticleGoogle Scholar