- Open Access
Role of A2B adenosine receptor-dependent adenosine signaling in multi-walled carbon nanotube-triggered lung fibrosis in mice
Journal of Nanobiotechnology volume 17, Article number: 45 (2019)
Multi-walled carbon nanotube (MWCNT)-induced lung fibrosis leads to health concerns in human. However, the mechanisms underlying fibrosis pathogenesis remains unclear. The adenosine (ADO) is produced in response to injury and serves a detrimental role in lung fibrosis. In this study, we aimed to explore the ADO signaling in the progression of lung fibrosis induced by MWCNT.
MWCNT exposure markedly increased A2B adenosine receptor (A2BAR) expression in the lungs and ADO level in bronchoalveolar lavage fluid, combined with elevation of blood neutrophils, collagen fiber deposition, and activation of myeloperoxidase (MPO) activity in the lungs. Furthermore, MWCNT exposure elicited an activation of transforming growth factor (TGF)-β1 and follistatin-like 1 (Fstl1), leading to fibroblasts recruitment and differentiation into myofibroblasts in the lungs in an A2BAR-dependent manner. Conversely, treatment of the selective A2BAR antagonist CVT-6883 exhibited a significant reduction in levels of fibrosis mediators and efficiently decreased cytotoxicity and inflammatory in MWCNT treated mice.
Our results reveal that accumulation of extracellular ADO promotes the process of the fibroblast-to-myofibroblast transition via A2BAR/TGF-β1/Fstl1 signaling in MWCNT-induced lung fibrosis.
Carbon nanotubes (CNTs) are new nanomaterials in a single layer (single-walled CNT, SWCNT) or concentric multi-layers (multi-walled CNT, MWCNT) with increasingly wide utilization in the fields of medicine, electronics, and structural engineering . However, because of the high demand for CNTs, it must be concerned that the health hazards of CNTs for human occupational and environmental exposure are more serious [2, 3]. One study reported MWCNT-containing airborne dust levels up to 400 μg/m3 in a research laboratory, although the total mass concentration reported in this study was not comprised exclusively of MWCNT . Furthermore, some animal studies have confirmed that pulmonary exposure to MWCNT results in fibrosis in the lungs [5,6,7].
Once exposure, MWCNTs deposit in the respiratory tract and increase lung burden, eventually leading to chronic inflammation and high risks of related adverse effects such as fibrosis . The pathologic development and features of CNT-induced pulmonary interstitial fibrosis overlap with those of irreversible pulmonary fibrosis (IPF) and pneumoconiosis considerably. IPF is the main cause of death due to unknown pathogeny and few treatment options. The mortality rate of IPF at 3–5 years after diagnosis is 50% . The fibrosis is progressive post-exposure and characterized by fibroblast proliferation and an excessive deposition of extracellular matrix (ECM) in the interstitium. Fibroblasts in granulation tissue differentiate into myofibroblasts, which has contractile phenotype and proliferates and synthesizes ECM components .
Secretion of inflammatory cytokines and infiltration of additional inflammatory leukocytes were observed after pulmonary exposure to MWCNT, which confirms the pulmonary inflammation produced by MWCNT [6, 11]. Elevated population of neutrophils is correlated with the acute inflammatory response . Myeloperoxidase (MPO) is a peroxidase enzyme that is synthesized and secreted by neutrophils and monocytes . MWCNT deposit efficiently and persistent in the respiratory tract, due to their pro-inflammatory potency represent one environmental factor proceeding to the progressive fibrotic lesions . There have been significant advances in understanding of MWCNT toxicity, yet the underlying mechanism of MWCNT-induced lung fibrosis remains elusive. High levels of extracellular adenosine (ADO) were produced in response to tissue injury and inflammation . Moreover, extracellular ADO levels are closely associated with the progression and severity of pulmonary fibrosis [16, 17]. Therefore, the aim of the present study is to determine the ability of ADO to elicit lung inflammation and exacerbate lung fibrosis in MWCNT treated mice.
In response to cellular stress, adenosine triphosphate (ATP) is released into extracellular and subsequently dephosphorylated to ADO by ecto-nucleotidases including ectonucleoside triphosphate diphosphohydrolase 1 (CD39) and Ecto-5′-nucleotidase (CD73) . ADO plays a principal role in the wound healing process. Under physiologic conditions, extracellular ADO level in cells and tissue fluids are in the nanomolar range, while ADO rises substantially during different forms of cellular distress . ADO orchestrates the cellular response by acting on ADO receptors, including A1 adenosine receptor (A1AR), A2AAR, A2BAR, and A3AR, of which A2BAR has emerged as a major mediator of chronic lung disease, such as fibrosis and tissue remodeling . A2BAR has the lowest affinity for ADO and is normally activated under excess accumulation of extracellular ADO. A2BAR levels are elevated in patients with IPF . The ADO signaling system has been closely linked with the production of several mediators, including interleukin-6 (IL-6)  and transforming growth factor (TGF)-β1 . In addition, ADO contributes to the differentiation of pulmonary fibroblasts into myofibroblasts, disease progression, and tissue remodeling via the engagement of the A2BAR . However, the ADO signaling involved in MWCNT-induced lung fibrosis is unknown until today.
TGF-β1 is a profibrotic cytokine that promotes myofibroblast activation and proliferation and plays a central role in the induction of fibrogenesis . Exaggerated TGF-β1 signaling contributes to accumulation of collagen and further ECM . Interestingly, the inhibition of A2BAR exerts an antifibrotic effect in chronic lung disease by preventing the expression of TGF-β1 . Therefore, there is a necessity to further characterize the A2BAR interacting with TGF-β1 signaling in MWCNT-induced lung fibrosis.
The hypothesis in this study is that the progressive inflammation, alveolar remodeling, and lung fibrosis induced by MWCNT are associated with progressive and proportionate increases in the level of extracellular ADO and the enhanced expression of A2BAR. Moreover, we speculate that CVT-6883 (a selective A2BAR antagonist) would reduce TGF-β1-mediated fibroblast proliferation and differentiation into myofibroblasts, and ultimately attenuate MWCNT-induced lung fibrosis.
Physicochemical characteristics and morphology of the MWCNT sample used in the present study are reported in Table 1. The surface morphology of MWCNTs is shown in micrograph images.
MWCNT-induced fibrotic phenotypes in mice
The histopathological changes in the MWCNT and DM groups have been shown in Fig. 1. Lung tissues were obtained at 1, 3, 7, and 14 days post-exposure. H&E staining showed interstitial thickening and bronchiolocentric inflammation in the mice exposure to MWCNT. The pathological changes reached a peak on day 7 and persisted throughout the 14-day post-exposure. As expected, aspiration of DM did not cause notable changes in the lungs (Fig. 1a).
We performed Masson’s trichrome staining to examine the fibrotic response directly. Abnormal collagen deposition was observed in the lung of MWCNT treatment on day 1 post exposure, progressed to a peak level on day 7, and maintained at a similar level throughout the day 14 (Fig. 1b). However, fibrotic mass formation was not observed in mice treated with DM.
MWCNTs exposure led to a significant increase in disease pathology compare to DM control (Fig. 1c). The fibrotic changes were quantified by using the Ashcroft score, which confirmed a significant increase of the fibrotic lesions in MWCNT treatment lungs compared with control at all the time points examined (Fig. 1d).
The effect of MWCNT on CD73, ADO, and A2BAR
Treatment of mice with MWCNT significantly increased CD73 gene expression on whole lung homogenate at 7 days post-exposure. However, CD73 gene expression appeared to be more variable at day 14 post exposure (Fig. 2a).
We measured the level of extracellular ADO, as defined by relative ADO level in bronchoalveolar lavage fluid (BALF). As expected, MWCNT treatment significantly elicited ADO level in BALF from day 3 to 14 (Fig. 2b).
MWCNT exposed mice exhibited significantly increased in the mRNA expression of A2BAR at 7 days post-exposure, and this elevation remained throughout 14 days after MWCNT exposure (Fig. 2c).
Inhibition of pulmonary inflammatory following treatment with CVT-6883
To evaluate MWCNT-induced inflammatory, we examined percentage of neutrophils in peripheral blood (Fig. 3a) and MPO activity (Fig. 3b) in the lung of mice. MWCNT induced a rapid increase in the percentage of neutrophils, and continued to increase on day 7 followed by a slightly reduction on day 14. MWCNT treatment enhanced MPO activity from day 7 to 14.
Based on this time course of fibrosis development induced by MWCNT, day 7 was chosen as the time point to reflect the MWCNT-induced lung injury. MWCNT exposure significantly increased lactate dehydrogenase (LDH) activity in serum (Fig. 3c) and percentage of neutrophils (Fig. 3d) in peripheral blood. Treatment with CVT-6883 caused a noticeable alleviation in LDH and percentage of neutrophils produced by MWCNT.
We further examined the protein levels of IL-6 in BALF (Fig. 3e) and lung tissues (Fig. 3f). The levels of IL-6 significantly increased in BALF and lung tissues of the MWCNT-induced group as compared with control mice. In contrast, this augmentation was significantly inhibited by the treatment of CVT-6883.
Treatment with CVT-6883 reduced profibrotic mediators in the lungs
MWCNT treatment resulted in a significant rise in TGF-β1 mRNA and protein expression. Moreover, our data showed that MWCNT treatment significantly promoted TGF-β1-stimulated Smad3 phosphorylation (p-Smad3) in lung tissues. Treatment of CVT-6883 showed a significant decline in TGF-β1 mRNA expression (Fig. 4a) and TGF-β1 and p-Smad3 protein levels (Fig. 4b).
Normalization of lung fibrosis in the lungs of CVT-6883-treated mice
To further determine the effect of A2BAR in the lung fibrosis of MWCNT exposure, we examined the protein level of two major ECM proteins (collagen I and fibronectin 1 (FN1)). As expected, CVT-6883 treatment inhibited the increased in collagen I and FN1 levels induced by MWCNT (Fig. 5a, b).
CVT-6883 inhibited fibroblast-to-myofibroblast transformation in mouse lungs
To determine whether A2BAR have the potential to directly induce fibrotic reactions characterized by increased differentiation of fibroblasts into myofibroblasts, we analyzed the effect of CVT-6883 on the expression of follistatin-like 1 (Fstl1) and fibroblast-to-myofibroblast transition markers: α-smooth muscle actin (α-SMA), platelet-derived growth factor receptor-β (PDGFR-β), heat shock protein 47 (HSP47), and fibroblast-specific protein 1 (FSP1). Fstl1 has the regulatory functions in cell proliferation and differentiation. As shown in Fig. 5c and d, MWCNT enhanced mRNA expression and protein level of Fstl1, while CVT-6883 inhibited Fstl1 expression. In addition, the protein levels of α-SMA, PDGFR-β, HSP47, and FSP1 were dramatically increased by MWCNT in the lungs (Fig. 6). However, CVT-6883 cotreatment suppressed the effects of MWCNT.
CNT exposure induced the pulmonary collagen deposition accompanied with pronounced acute inflammation preceding chronic fibrosis progression. Serum LDH activities reflects the cellular injury after MWCNT exposure. To further evaluate potential pulmonary inflammation induced by MWCNT, the level of proinflammatory cytokines IL-6 and MPO activity between the BALF and lung tissues was examined. In our study, MWCNT induced pulmonary inflammatory response by recruiting and activating neutrophils in the lungs through movement of circulating leukocytes to the lungs. Previous studies have shown that MWCNT-induced inflammation is probably due to phagolysosome membrane permeability, which has been implicated in the activation of IL-6 . Notably, CVT-6883, as an inhibitor of A2BAR, greatly ameliorated pulmonary inflammation, resulting in a significant reduction in fibrosis. Based on these results, collagen deposition caused by MWCNTs is related to the proinflammatory effects of MWCNTs. Notably, the blockade of A2BAR restores cellular injury and inflammatory effects, thereby alleviating the progression of lung fibrosis.
We firstly examined the expression of CD73 following MWCNT exposure. Interestingly, MWCNT-induced lung fibrosis significantly increased CD73 gene expression and ADO levels. This finding is consistent with CD73-mediated enzymatic conversion of adenosine monophosphate (AMP) to ADO in the lungs of mice with radiation-induced pulmonary fibrosis . In addition, ADO also increased CD73 through transcriptional regulation via cyclic AMP response element in the CD73 promoter . Chronic inflammation was associated with a constant increase in CD73+ leukocytes in the lung and an accumulation of CD73+ T cells, during the fibrotic phase . CD73 was up-regulated in lung biopsy samples from patients with stage 4 chronic obstructive pulmonary disease or severe idiopathic pulmonary fibrosis, respectively . Moreover, reduced extracellular ADO accumulation in radiation treated CD73−/− mice prevented fibrosis development . Thus, the necessity of ADO production of nucleoside signaling can be confirmed, and CD73 activation and ADO accumulation potentiates lung fibrosis after MWCNT treatment.
In the present study, elevations in extracellular ADO activated A2BAR, which promoted MWCNT-induced lung fibrosis through activating TGF-β1. Elevated expression of A2BAR has been detected in several chronic lung diseases, such as chronic obstructive pulmonary disease and lung fibrosis [21, 23]. The role of A2BAR stimulation or blockade in cell proliferation has been depending on the cell type and culture condition [31, 32]. Of note, A2BAR stimulated TGF-β synthesis in lung fibroblast cells . Furthermore, A2B-null mice exhibit slightly effects in acute lung injury but reduced lung fibrosis, suggesting that A2BAR promote fibrosis . We therefore determined whether A2BAR modulates TGF-β1 signaling in CNT-induced lung fibrosis. The TGF-β1/Smads signaling pathway occurs as a result of receptor-ligand interactions resulting in the expression of a number of TGF-β1 target genes through the rapid phosphorylation and nuclear translocation of Smad3 . Inhibition of TGF-β/Smad signaling pathway is an effective approach to treat fibrotic disorders . Our results showed that MWCNT remarkably stimulated the expression of TGF-β1 and Smad3 phosphorylation in the lungs in an A2BAR-dependent manner. These data identified the A2BAR as an upstream modulator of TGF-β1 and can be a potential therapeutic target in MWCNT induced lung fibrosis.
Large amounts of ECM remodels connective tissue into dense scar tissue, and ultimately leads to a disruption of organ architecture and loss of function . TGF-β1 plays a central role in the ECM proteins production (such as collagen I and FN1) in the lungs after MWCNT exposure [10, 38]. Inhibition of TGF-β1 signaling by Smad3 inactivation was partially resistance to pulmonary fibrosis . The results of present study are also consistent with this because MWCNT increased the production of collagen I and FN1 where TGF-β1 signaling was activated. Moreover, our study showed that induction of collagen I and FN1 was blocked by co-treating with A2BAR inhibitor CVT-6883, confirming the critical role of A2BAR in MWCNT-induced deposition of fibrous ECM. Altogether, the antagonism of A2BAR potentially suppresses the TGF-β1 signaling activation and thereby inhibits ECM production and deposition during MWCNT-induced lung fibrosis.
Lung fibrosis is characterized by excessive accumulation of α-SMA-expressing myofibroblasts arising from interactions with TGF-β1 and mechanical influences . Fibroblasts/myofibroblasts are major effector cells in production of ECM proteins and airway remodeling . Fstl1 is associated with myofibroblast accumulation and subsequently ECM production that is mediated by canonical TGF-β signaling [42, 43]. Previous study showed that MWCNTs increased the myofibroblast population by promoting fibroblasts proliferation and differentiation . Here, blocking A2BAR signaling using CVT-6883 markedly attenuated Fstl1 induction in MWCNT-treated lung tissue. We further examined the effects of A2BAR in fibroblasts and myofibroblasts during MWCNT-exposed lungs using HSP47 and FSP1 as markers for fibroblasts and, α-SMA and PDGFR-β for myofibroblasts [44,45,46]. Our study found that MWCNT remarkably increased numbers of fibroblasts and myofibroblasts in the lungs in an A2BAR-dependent manner. Collectively, MWCNT elevates A2BAR expression, which promotes Fstl1-induced fibroblasts proliferation and differentiation.
In conclusion, our study identified that excesses extracellular ADO level promoted lung fibrosis following MWCNT exposure, which involved the engagement of the A2BAR. Antagonism of A2BAR attenuated TGF-β1-induced fibroblast proliferation and differentiation, thereby inhibiting collagen deposition and progressive pulmonary fibrogenesis induced by MWCNT (Fig. 7). To the best of our knowledge, modulation of ADO levels and antagonism of A2BAR-mediated responses may be a novel therapeutic approach for MWCNT-induced lung fibrosis.
MWCNT materials and preparation
The MWCNT (TNM7, purity > 98%) has a surface area of > 100 m2/g, < 1.5 wt% ash, 0.22 g/cm3 tap density, and the nanotube was obtained from Chengdu Organic Chemistry Co., Ltd, Chinese Academy of Sciences (Chengdu, China). Data were provided by the manufacturer. TNM7 is produced by natural gas catalytic decomposition over Ni-based catalyst. The samples were observed using a Hitachi SU 8010 field emission scanning electron microscope (Hitachi, Japan). MWCNT was suspended in dispersion medium (DM) as previously described [47, 48]. DM is Ca2+ and Mg2+-free phosphate buffered saline (PBS), pH 7.4, supplemented with 5.5 mM d-glucose, 0.6 mg/ml mouse serum albumin (Sigma-Aldrich, St. Louis, MO, USA), and 0.01 mg/ml 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (Sigma-Aldrich).
Six to eight weeks male C57BL/6 mice were purchased from Liaoning Changsheng Technology Industrial Co., LTD (Liaoning, China). All experiments involving animals were in accordance with the Ethical Committee for Animal Experiments of Northeast Agricultural University. The mice were housed under environmental conditions (22 ± 2 °C, 55 ± 5% relative humidity) with a 12 h light/dark cycle, and were provided with standard pelleted rodent diet.
A single dose of 50 μl of DM only, or 50 μl of DM containing 40 μg MWCNT was administered by pharyngeal aspiration, which is an alternative to inhalation of administration to deliver a specific dose of an agent into mouse lungs and represents a noninvasive route .
Some mice were treatment with CVT-6883 (1 mg/kg, Tocris) in the morning and in the evening (interval was 12 h) for 5 days by intraperitoneal injection. The same formulation and dose of CVT-6883 described above was used in MWCNT studies, where twice daily intraperitoneal injections were given on days 3–7 of the protocol [26, 50].
Tissue collection and histopathology
The left lobe of the lung was inflated and fixed in 10% neutral buffered formalin for hematoxylin and eosin (H&E) and Masson’s Trichrome. Histological analysis of lung pathology scoring was obtained from stained lung tissue . Fibrotic changes were quantified using the modified Ashcroft scale . The right lung lobes were collected for mRNA and protein analysis.
Blood samples were collected from all animals in EDTA-containing vacutainer tubes. Percentage of neutrophils in peripheral blood of mice were obtained using an automated Auto Hematology Analyzer BC-2600Vet (Mindray, Shenzhen, China).
We also obtained the serum after centrifugated at 3000 × rpm for 10 min at 4 °C. All serum samples were hemolysis-free. Serum LDH activities were measured with a Uni Cel DxC Synchron chemistry system (Beckman Coulter Inc., Fulton, CA, USA).
Measurement of MPO activity
The lung tissues were homogenized and dissolved in extraction buffer for the analysis of MPO activity . To assess the accumulation of neutrophils in the lung tissues, MPO activities were detected following the respective manufacturer’s instructions (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).
Bronchoalveolar lavage fluid ADO level
Mice were euthanized for collecting the BALF. Briefly, lungs were lavaged 4 times with 0.3 ml PBS containing 10 μM dipyridamole (Sigma-Aldrich), 10 μM ADA-inhibitor deoxycoformycin (MedChem Express, USA), and 10 μM adenosine 5′-(α,β-methylene) diphosphate (Sigma-Aldrich). The BALF was centrifuged (3000 g × 5 min) to remove cells and debris. Twenty microliters of BALF supernatant was analyzed by high-performance liquid chromatography (LC-10AT, Japan) using a 5 µm Hypersil ODS column (250 × 4.6 mm, Dalian Elite Analytical Instruments Co. Ltd, Dalian, China) and a gradient of solutions A (methyl alcohol) and B (0.02 M NH4H2PO4, pH 5.1) at a flow rate of 1 ml/min and run. The ADO peaks were identified and quantified by known external standard curves.
Analysis of mRNA
Total RNA was isolated from frozen mouse lung tissues using TRIzol reagent (Invitrogen). Real-time quantitative PCR (RT-qPCR) were carried out by a LightCycler 480 II instrument (Roche, Basel, Switzerland) using SYBR Green master mix. Specific oligonucleotide primers used are as follows: CD73, forward: 5′-ATCCGCAAGGAAGAACCC-3′, reverse: 5′-AGTGCCATAGCATCGTAGCC-3′; A2BAR, forward: 5′-GAGACTTCCGCTACAGTTTCCA-3′, reverse: 5′-TCATAAGCCCAGACTGAGAGTAGAC-3′; TGF-β1, Sense: 5′-TGAGTGGCTGTCTTTTGACG-3′, Antisense: 5′-TCTCTGTGGAGCTGAAGCAA-3′; Fstl1, forward: 5′-TTATGATGGGCACTGCAAAGAA-3′, reverse: 5′-ACTGCCTTTAGAGAACCAGCC-3′; 18 S ribosomal RNA, forward: 5′-GTAACCCGTTGAACCCCATT-3′, reverse: 5′-CCATCCAATCGGTAGTAGCG-3′. 18 S ribosomal RNA were used as an internal control. Calculations were performed by a comparative 2−∆∆CT method.
Enzyme-linked immunosorbent assay
The concentration of IL-6 in the BALF was measured by Enzyme-linked immunosorbent assay (ELISA) following the manufacturer’s protocols (R&D Systems, Minneapolis, USA).
Western blot analysis
Immunoblot analysis was performed as previously described [53, 54] with use of the following antibodies: TGF-β1, collagen I, PDGFR-β, α-SMA, Smad3, p-Smad3 (Cell Signaling Technologies), Fstl1 (R&D Systems), IL-6, HSP47 (Santa Cruz Biotechnology), FSP1 (Sigma-Aldrich), FN1 (Sigma-Aldrich), and HRP-labeled goat anti-mouse IgG or goat anti-rabbit IgG antibody peroxidase-conjugated (ZSGB-BIO, Beijing, China). GAPDH (Hangzhou Goodhere Biotechnology, Hangzhou, China) was used as an internal control for normalization of protein expression.
Results are expressed as mean ± SEM. Differences among groups were evaluated by one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test. A p-value < 0.05 was considered as significant. Statistical analyses were carried out using SPSS 19.0 software (SPSS, Chicago, IL, USA).
A2B adenosine receptor
α-smooth muscle actin
bronchoalveolar lavage fluid
ectonucleoside triphosphate diphosphohydrolase 1
fibroblast-specific protein 1
heat shock protein 47
irreversible pulmonary fibrosis
multi-walled carbon nanotube
platelet-derived growth factor receptor-β
transforming growth factor-β1
Vietti G, Lison D, van den Brule S. Mechanisms of lung fibrosis induced by carbon nanotubes: towards an adverse outcome pathway (AOP). Part Fibre Toxicol. 2016;13:11.
Polimeni M, Gulino GR, Gazzano E, Kopecka J, Marucco A, Fenoglio I, et al. Multi-walled carbon nanotubes directly induce epithelial-mesenchymal transition in human bronchial epithelial cells via the TGF-β-mediated Akt/GSK-3β/SNAIL-1 signalling pathway. Part Fibre Toxicol. 2016;13(1):27.
Chatterjee N, Yang J, Yoon D, Kim S, Joo SW, Choi J. Differential crosstalk between global DNA methylation and metabolomics associated with cell type specific stress response by pristine and functionalized MWCNT. Biomaterials. 2017;115:167–80.
Porter DW, Hubbs AF, Mercer RR, Wu N, Wolfarth MG, Sriram K, et al. Mouse pulmonary dose- and time course-responses induced by exposure to multi-walled carbon nanotubes. Toxicology. 2010;269(2–3):136–47.
Dong J, Ma Q. Macrophage polarization and activation at the interface of multi-walled carbon nanotube-induced pulmonary inflammation and fibrosis. Nanotoxicology. 2018;12(2):153–68.
Nikota J, Banville A, Goodwin LR, Wu D, Williams A, Yauk CL, et al. Stat-6 signaling pathway and not Interleukin-1 mediates multi-walled carbon nanotube-induced lung fibrosis in mice: insights from an adverse outcome pathway framework. Part Fibre Toxicol. 2017;14(1):37.
Wang X, Liao YP, Telesca D, Chang CH, Xia T, Nel AE. The Genetic Heterogeneity among different mouse strains impacts the lung injury potential of multiwalled carbon nanotubes. Small. 2017;13:33.
Schwotzer D, Ernst H, Schaudien D, Kock H, Pohlmann G, Dasenbrock C, et al. Effects from a 90-day inhalation toxicity study with cerium oxide and barium sulfate nanoparticles in rats. Part Fibre Toxicol. 2017;14(1):23.
Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011;183(6):788–824.
Dong J, Ma Q. Myofibroblasts and lung fibrosis induced by carbon nanotube exposure. Part Fibre Toxicol. 2016;13(1):60.
Duke KS, Bonner JC. Mechanisms of carbon nanotube-induced pulmonary fibrosis: a physicochemical characteristic perspective. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2018;10(3):e1498.
Qu G, Liu W, Zhao Y, Gao J, Xia T, Shi J, et al. Improved biocompatibility of black phosphorus nanosheets by chemical modification. Angew Chem Int Ed Engl. 2017;56(46):14488–93.
Amirshahrokhi K. Anti-inflammatory effect of thalidomide in paraquat-induced pulmonary injury in mice. Int Immunopharmacol. 2013;17(2):210–5.
Chu H, Jiang S, Liu Q, Ma Y, Zhu X, Liang M, et al. Sirtuin1 protects against systemic sclerosis-related pulmonary fibrosis by decreasing proinflammatory and profibrotic processes. Am J Respir Cell Mol Biol. 2018;58(1):28–39.
Borea PA, Gessi S, Merighi S, Vincenzi F, Varani K. Pathologic overproduction: the bad side of adenosine. Br J Pharmacol. 2017;174(13):1945–60.
Luo F, Le NB, Mills T, Chen NY, Karmouty-Quintana H, Molina JG, et al. Extracellular adenosine levels are associated with the progression and exacerbation of pulmonary fibrosis. FASEB J. 2016;30(2):874–83.
Volmer JB, Thompson LF, Blackburn MR. Ecto-5′-Nucleotidase (CD73)-mediated adenosine production is tissue protective in a model of bleomycin-induced lung injury. J Immunol. 2006;176(7):4449–58.
Liu H, Xia Y. Beneficial and detrimental role of adenosine signaling in diseases and therapy. J Appl Physiol. 2015;119(10):1173–82.
Karmouty-Quintana H, Xia Y, Blackburn MR. Adenosine signaling during acute and chronic disease states. J Mol Med (Berl). 2013;91(2):173–81.
Philip K, Mills TW, Davies J, Chen NY, Karmouty-Quintana H, Luo F, et al. HIF1A up-regulates the ADORA2B receptor on alternatively activated macrophages and contributes to pulmonary fibrosis. FASEB J. 2017;31(11):4745–58.
Karmouty-Quintana H, Philip K, Acero LF, Chen NY, Weng T, Molina JG, et al. Deletion of ADORA2B from myeloid cells dampens lung fibrosis and pulmonary hypertension. FASEB J. 2015;29(1):50–60.
Chunn JL, Mohsenin A, Young HW, Lee CG, Elias JA, Kellems RE, et al. Partially adenosine deaminase-deficient mice develop pulmonary fibrosis in association with adenosine elevations. Am J Physiol Lung Cell Mol Physiol. 2006;290(3):L579–87.
Karmouty-Quintana H, Weng T, Garcia-Morales LJ, Chen NY, Pedroza M, Zhong H, et al. ADORA2B and hyaluronan modulate pulmonary hypertension associated with chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol. 2013;49(6):1038–47.
Tsoyi K, Chu SG, Patino-Jaramillo NG, Wilder J, Villalba J, Doyle-Eisele M, et al. Syndecan-2 attenuates radiation-induced pulmonary fibrosis and inhibits fibroblast activation by regulating PI3 K/Akt/ROCK pathway via CD148. Am J Respir Cell Mol Biol. 2018;58(2):208–15.
Wei Y, Kim TJ, Peng DH, Duan D, Gibbons DL, Yamauchi M, et al. Fibroblast-specific inhibition of TGF-β1 signaling attenuates lung and tumor fibrosis. J Clin Invest. 2017;127(10):3675–88.
Sun CX, Zhong H, Mohsenin A, Morschl E, Chunn JL, Molina JG, et al. Role of A2B adenosine receptor signaling in adenosine-dependent pulmonary inflammation and injury. J Clin Invest. 2006;116(8):2173–82.
Hamilton RF Jr, Wu Z, Mitra S, Shaw PK, Holian A. Effect of MWCNT size, carboxylation, and purification on in vitro and in vivo toxicity, inflammation and lung pathology. Part Fibre Toxicol. 2013;10(1):57.
Wirsdörfer F, de Leve S, Cappuccini F, Eldh T, Meyer AV, Gau E, et al. Extracellular adenosine production by ecto-5′-Nucleotidase (CD73) enhances radiation-induced lung fibrosis. Cancer Res. 2016;76(10):3045–56.
Zhou Y, Murthy JN, Zeng D, Belardinelli L, Blackburn MR. Alterations in adenosine metabolism and signaling in patients with chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. PLoS ONE. 2010;5(2):e9224.
de Leve S, Wirsdörfer F, Cappuccini F, Schütze A, Meyer AV, Röck K, et al. Loss of CD73 prevents accumulation of alternatively activated macrophages and the formation of prefibrotic macrophage clusters in irradiated lungs. FASEB J. 2017;31(7):2869–80.
Phosri S, Arieyawong A, Bunrukchai K, Parichatikanond W, Nishimura A, Nishida M, et al. Stimulation of Adenosine A2B receptor inhibits endothelin-1-induced cardiac fibroblast proliferation and α-smooth muscle actin synthesis through the cAMP/Epac/PI3K/Akt-signaling pathway. Front Pharmacol. 2017;8:428.
Giacomelli C, Daniele S, Romei C, Tavanti L, Neri T, Piano I, et al. The A2B adenosine receptor modulates the epithelial– mesenchymal transition through the balance of cAMP/PKA and MAPK/ERK pathway activation in human epithelial lung cells. Front Pharmacol. 2018;9:54.
Fang M, Xia J, Wu X, Kong H, Wang H, Xie W, et al. Adenosine signaling inhibits CIITA-mediated MHC class II transactivation in lung fibroblast cells. Eur J Immunol. 2013;43(8):2162–73.
Zhou Y, Schneider DJ, Morschl E, Song L, Pedroza M, Karmouty-Quintana H, et al. Distinct roles for the A2B adenosine receptor in acute and chronic stages of bleomycin-induced lung injury. J. Immunol. 2011;186:1097–106.
Zhou XM, Wang GL, Wang XB, Liu L, Zhang Q, Yin Y, et al. GHK peptide inhibits bleomycin-induced pulmonary fibrosis in mice by suppressing TGFβ1/Smad-mediated epithelial-to-mesenchymal transition. Front Pharmacol. 2017;8:904.
Bian C, Qin WJ, Zhang CY, Zou GL, Zhu YZ, Chen J, et al. Thalidomide (THD) alleviates radiation induced lung fibrosis (RILF) via down-regulation of TGF-β/Smad3 signaling pathway in an Nrf2-dependent manner. Free Radic Biol Med. 2018;129:446–53.
Murtha LA, Schuliga MJ, Mabotuwana NS, Hardy SA, Waters DW, Burgess JK, et al. The processes and mechanisms of cardiac and pulmonary fibrosis. Front Physiol. 2017;8:777.
Hinz B, Phan SH, Thannickal VJ, Prunotto M, Desmoulière A, Varga J, et al. Recent developments in myofibroblast biology: paradigms for connective tissue remodeling. Am J Pathol. 2012;180(4):1340–55.
Dong C, Gongora R, Sosulski ML, Luo F, Sanchez CG. Regulation of transforming growth factorbeta1 (TGF-β1)-induced pro-fibrotic activities by circadian clock gene BMAL1. Respir Res. 2016;17:4.
Ryu C, Sun H, Gulati M, Herazo-Maya JD, Chen Y, Osafo-Addo A, et al. Extracellular mitochondrial DNA is generated by fibroblasts and predicts death in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2017;196(12):1571–81.
Liu G, Cooley MA, Nair PM, Donovan C, Hsu AC, Jarnicki AG, et al. Airway remodelling and inflammation in asthma are dependent on the extracellular matrix protein fibulin-1c. J Pathol. 2017;243(4):510–23.
Dong Y, Geng Y, Li L, Li X, Yan X, Fang Y, et al. Blocking follistatin-like 1 attenuates bleomycin-induced pulmonary fibrosis in mice. J Exp Med. 2015;212(2):235–52.
Zheng X, Qi C, Zhang S, Fang Y, Ning W. TGF-β1 induces Fstl1 via the Smad3—c-Jun pathway in lung fibroblasts. Am J Physiol Lung Cell Mol Physiol. 2017;313(2):L240–51.
Dong J, Ma Q. TIMP1 promotes multi-walled carbon nanotube induced lung fibrosis by stimulating fibroblast activation and proliferation. Nanotoxicology. 2017;11(1):41–51.
Wang P, Wang Y, Nie X, Braïni C, Bai R, Chen C. Multiwall carbon nanotubes directly promote fibroblast-myofibroblast and epithelial–mesenchymal transitions through the activation of the TGF-β/Smad signaling pathway. Small. 2015;11(4):446–55.
Kakugawa T, Mukae H, Hayashi T, Ishii H, Abe K, Fujii T, et al. Pirfenidone attenuates expression of HSP47 in murine bleomycin-induced pulmonary fibrosis. Eur Respir J. 2004;24(1):57–65.
Porter D, Sriram K, Wolfarth M, Jefferson A, Schwegler-Berry D, Andrew M, et al. A biocompatible medium for nanoparticle dispersion. Nanotoxicology. 2008;2(3):144–54.
Dong J, Ma Q. Suppression of basal and carbon nanotube-induced oxidative stress, inflammation and fibrosis in mouse lungs by Nrf2. Nanotoxicology. 2016;10(6):699–709.
Dong J, Ma Q. Osteopontin enhances multi-walled carbon nanotube-triggered lung fibrosis by promoting TGF-β1 activation and myofibroblast differentiation. Part Fibre Toxicol. 2017;14(1):18.
Mustafa SJ, Nadeem A, Fan M, Zhong H, Belardinelli L, Zeng D. Effect of a specific and selective A2B adenosine receptor antagonist on adenosine agonist AMP and allergen-induced airway responsiveness and cellular influx in a mouse model of asthma. J Pharmacol Exp Ther. 2007;320(3):1246–51.
Brown TA, Lee JW, Holian A, Porter V, Fredriksen H, Kim M, et al. Alterations in DNA methylation corresponding with lung inflammation and as a biomarker for disease development after MWCNT exposure. Nanotoxicology. 2016;10(4):453–61.
Liu BY, Yu HX, Baiyun RQ, Lu JJ, Li SY, Bing QZ, et al. Protective effects of dietary luteolin against mercuric chloride-induced lung injury in mice: involvement of AKT/Nrf2 and NF-κB pathways. Food Chem Toxicol. 2018;113:296–302.
Liu BY, Jiang HJ, Lu JJ, Baiyun RQ, Li SY, Lv YY, et al. Grape seed procyanidin extract ameliorates lead-induced liver injury via miRNA153 and AKT/GSK-3β/Fyn-mediated Nrf2 activation in rats. J Nutr Biochem. 2018;52:115–23.
Zhang ZG, Li SY, Jiang HJ, Liu BY, Lv ZJ, Guo CM, et al. Effects of selenium on apoptosis and abnormal amino acid metabolism induced by excess fatty acid in isolated rat hepatocytes. Mol Nutr Food Res. 2017;61(9):1700016.
BYL and ZGZ designed and finished the experiments and finalized the article. QZB contributed sample materials. QZB and SYL supervised and analysed experiments and data. BH and JJL performed gene expression analyses. RQBY and XYZ performed protein analysis. QYL and HW performed the high-performance liquid chromatography assessment and commercial kit. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
All data and materials are included in the manuscript.
Consent for publication
Ethics approval and consent to participate
All experiments involving animals were in accordance with the Ethical Committee for Animal Experiments of Northeast Agricultural University.
This work was funded by the University Nursing Program for Young Scholar with Creative Talents in Heilongjiang Province (UNPYSCT-2016012), National Natural Science Foundation of China (31101868), Financial Assistance from Postdoctoral Scientific Research Developmental Fund of Heilongjiang Province (LBH-Q16013), Scientific Research Foundation for the Returned Overseas Chinese Scholars of Heilongjiang Province (LC2017007).
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Liu, B., Bing, Q., Li, S. et al. Role of A2B adenosine receptor-dependent adenosine signaling in multi-walled carbon nanotube-triggered lung fibrosis in mice. J Nanobiotechnol 17, 45 (2019) doi:10.1186/s12951-019-0478-y
- Multi-walled carbon nanotubes
- Lung fibrosis
- A2B adenosine receptor
- Transforming growth factor-β1
- Follistatin-like 1
- Fibroblast-to-myofibroblast transition
- High-performance liquid chromatography