Application of in situ reverse trancriptase-polymerase chain reaction (RT-PCR) to tissue microarrays
© Stamps et al; licensee BioMed Central Ltd. 2003
Received: 29 April 2003
Accepted: 28 May 2003
Published: 28 May 2003
Detection of disease-associated gene transcripts in primary disease tissues is frequently confounded by the presence of non-involved cell types. Alternative methods of detecting gene expression directly within tissues involve either the generation of antibodies, which can be a lengthy process and may suffer from lack of specificity, or amplification of reverse-transcribed cDNA in tissue sections (in situ RT-PCR). The latter method is highly specific and enables detection of transcripts in the cells originally responsible for their synthesis, but is highly destructive of tissue structures and can be carried out on only one or a few sections per experiment, resulting in low reproducibility. In this study, in situ RT-PCR was applied for the first time to commercially available tissue section microarrays enabling the examination of up to 70 different samples simultaneously. Modifications to the technique are detailed that preserved visible tissue and cellular structures and improved transcript detection whilst preventing significant generation of artefacts.
Prior to the advent of miniaturisation, the study of cellular gene expression took the form of either antibody-protein detection, such as Western blotting of protein lysates or immunohistochemistry (IHC) on tissue sections or immobilised tissue culture cells, or nucleic acid analyses such as Northern blot hybridisation of RNA transcripts or PCR amplification of reverse-transcribed cDNA. Miniaturisation technologies are now long established in the measurement of RNA expression levels, in the form of nucleic acid microarray. Compared to classical Northern blotting or even the small amounts of material required for PCR, the microarray presents significant economies of scale and can equal or better the specificity of other techniques, including the detection of single nucleotide polymorphisms and splice variants. High throughput is, however, expensive, and particularly in clinical studies may not be practical from the point of view of sample sizes. Primary samples are also heterogeneous and although microarray and other techniques may reveal variations in gene expression, they do not identify the cell type responsible for the differential. Although the use of antibodies in IHC has the advantage of detecting in situ the protein product of gene expression, the origin of secreted proteins such as growth factors, cytokines and serum markers may not be revealed by this technique. Miniaturisation of protein detection has given rise to some notable technologies e.g. surface plasmon resonance and emerging 'protein chip' platforms. This area of development is less advanced than genomic microarray and faces greater challenges due to the less predictable nature of protein interactions in solution, and the greater difficulty in synthesising, and optimising conditions for detection molecules.
The specific amplification of cytosolic mRNA molecules in paraffin-embedded tissue sections was first reported by Staecker et al. , using fluorescence detection of amplified molecules. Use of the technique is not as widespread as other RT-PCR methods, however, and this may be due to technical complexity and an inherent lack of reproducibility [2, 3]. The processing of large numbers of samples is also slow and sequential, adding to variability issues.
We present for the first time, the application of in situ RT-PCR to the detection of specific RNA transcripts in histological microarrays of up to 250 different samples per slide, using modifications of the procedure to maximise reliability and sensitivity. The modified method may be carried out entirely using commercially available materials, including tissue microarrays.
The use of in situ RT-PCR to examine gene expression in disease tissues has certain advantages over more established hybridisation, PCR amplification or antibody-based techniques. As with immunohistochemistry, detection of gene expression is at the level of individual cells , but whereas polyclonal antibody production by immunisation may take 4 months or longer, and require extensive optimisation, it is relatively easy to characterise and optimise oligonucleotide primers which have considerably less chemical complexity and, therefore, inherently more predictable properties. Moreover, while cross-reactivity is a frequent problem when selecting antibodies for protein detection, it is a simple matter to select PCR primers that are specific to a single member of a gene family, or even a particular splice variant of that gene.
We have successfully applied in situ RT-PCR to 1 mm paraffin-embedded tissue section arrays in order to determine which cells within a cancer are responsible for gene over-expression observed in RNA extracts. A number of technical manipulations were incorporated into the in situ protocol to ensure specificity and fidelity, and these transferred readily to the micro-array format. To our knowledge, this is the first time this procedure has been applied simultaneously to multiple samples in a microarray format.
A DNAse digestion step is commonly used in RT-PCR amplification in order to reduce the risk of spurious amplification of genomic DNA [8–10]. This can also be carried out on tissue sections  but the extensive incubation time required (up to 16 hr) means that considerable tissue autolysis occurs, damaging tissue structure and making post-PCR identification of cells difficult. In our protocol, the DNAse digestion step was omitted so as to better preserve tissue structure. Modifications to experimental design were employed to prevent amplification of genomic DNA. Although other approaches have been taken to obviate nuclease pre-treatment , we employed more conventional means. Firstly, primers were designed to amplify across two different exons, so that the amplified fragment from reverse transcribed, fully spliced mRNA would be small (300 bp), whilst the distance between the same primer sites in genomic DNA was over 3500 bp. Secondly, the number of PCR cycles and the duration of the polymerisation step were minimised so that any priming from genomic DNA would fail to achieve chain-reaction amplification. These strategies had a number of other beneficial effects: the PCR cycle number was kept with the linear range of amplification established by real-time quantitative RT-PCR, giving a more quantitative representation of the mRNA remaining in each cell, and avoiding significant synthesis of non-specific artifacts. Diffusion of reaction products away from the site of synthesis, another problem associated with in situ PCR , was reduced by this rapid procedure and exposure of the tissue sections to destructive conditions was also minimised, with the result that post-amplification staining revealed a high degree of preservation of tissue architecture and cellular features.
A consequence of using low PCR cycle numbers is that the degree of amplification will be limited, with implications for detection of the PCR product. Standard peroxidase-linked antibody detection is insufficiently sensitive. Chemiluminescent or fluorescent detection reagents could be used instead to amplify the signal, but these would require specialised image detection systems and would rapidly diffuse away from the point of detection. Immunogold labelling followed by silver nucleation produced solid particles visible by light microscopy at magnifications suitable for visualising tissue and cellular features. This enabled simultaneous imaging of PCR products and hematoxylin-stained tissue details. The silver particles were bound to PCR products via anti-digoxygenin antibodies, and proved resistant to diffusion, remaining in the same cellular localisation as the original mRNA.
A persistent problem with the in situ PCR procedure has been inconsistency of results. Dedicated instrumentation has been designed with the aim of controlling conditions on a microscope slide, and some machines accommodate four or more slides to increase throughput and lower experimental variability. However, variation in the quality of paraffin-embedded tissue sections, and the number of steps involved in in situ PCR and the time taken to acquire data on significant numbers of samples affect the reproducibility of the technique. We found that a single, standard in situ PCR coverslip covered up to seventy 1 mm sections on a Clinomics tissue microarray, enabling simultaneous amplification of reverse transcribed RNA in each section under selected conditions. Although small tissue sections are more likely to become dislodged during the process of de-waxing and amplification, the use of poly-L-lysine coated slides decreased these losses and the cancer tissues examined were intrinsically more adherent due to their high cellularity. Thus a significant number of tissue samples could be analysed per single experiment. This approach substantially addresses the problem of slide-to-slide variability by subjecting large numbers of samples to identical experimental conditions. In addition, our technical modifications minimised tissue damage during preparation and amplification, preserving useful information on cellular morphology.
In situ PCR can be successfully applied to tissue microarrays for the specific detection and cellular localisation of transcriptional expression. The analysis of up to 70 sections in a single amplification experiment addresses the problem of experimental variability associated with this method. Modifications were introduced into the procedure aimed at reducing sample degradation, resulting in preservation of tissue and subcellular structures and reducing diffusion of labelled PCR products. Methods were carried out using entirely commercially available reagents, in order to develop a standardised procedure for visualisation of mRNA expression in situ.
Quantitative Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR)
Real-time quantitative RT-PCR analysis of gene expression [13, 14] was carried out on first-strand cDNA derived from RNA isolated from samples of normal and tumour tissues. Each PCR reaction contained 10 ng first-strand cDNA (prepared from each mRNA sample using SuperscriptTM reverse transcriptase, Life Technologies, Carlsbad, CA), SYBR green sequence detection reagents (Applied Biosystems, Foster City, CA), and sense and anti-sense primers. The primers used to amplify spondin-2 were: sense, 5'-CTCGTTTGTGGTGCGCATCGTG-3'; antisense, 5'-CAGGGAGACCTCGCAGTCCAGC-3'. The thermal cycling parameters were; 1 cycle of 94°C for 2.5 minutes followed by 40 cycles of 94°C for 40 seconds, 60°C for 50 seconds, 72°C for 30 seconds. Real-time quantitative RT-PCR was assayed on an ABI Prism 7700 sequence detection system (Applied Biosystems, Foster City, CA) and the accumulation of PCR product was measured in real time as the increase in SYBR green fluorescence. Data was analyzed using the Sequence Detector program v1.6.3 (Applied Biosystems, Foster City, CA). Standard curves relating initial template copy number to fluorescence and amplification cycle were generated using the amplified PCR product as a template, and were used to calculate mRNA copy number in each sample. Data were expressed as relative mRNA expression.
In Situ RT-PCR
Direct in situ RT-PCR detection of spondin-2 mRNA expression was examined in formalin fixed, paraffin embedded prostate cancer tissues (Clinomics Biosciences, Inc., Frederick, MD), arranged on microscope slides in arrays of up to 250 sections, each 1 mm in diameter. The tissue was de-waxed in xylene, gradually re-hydrated through alcohol and washed in phosphate buffered saline (PBS) before being permeabilised in 0.01% Triton X-100 for 3 minutes followed by treatment with Proteinase K for 30 minutes at 37°C. Direct in situ RT-PCR was carried out in a GeneAmp In Situ PCR System 1000 (Perkin Elmer Biosystems, Foster City, CA) using a GeneAmp Thermostable rTth RT-PCR kit (Perkin Elmer Biosystems, Foster City, CA). In addition to the spondin-2 specific primers described above, the following 'scrambled' primers were used for control amplifications: 5'-GTTGCGATCGTGCTGTGCGTCT-3'; 5'-CGACGCTAGCTCAGCACGCGAG-3'. The thermal cycling parameters were; 1 cycle of 94°C for 2.5 minutes followed by 20 cycles of 94°C for 40 seconds, 60°C for 50 seconds, 72°C for 30 seconds. Amplified product was detectable through the direct incorporation of alkali stable digoxigenin-11-deoxyuridine triphosphate (dUTP; Roche Diagnostics Ltd., Basel, Switzerland) which was added to the reaction mix according to the manufacturer's recommendation. After washing in PBS, 10 ul Anti-Digoxigenin-Gold antibody (Roche Diagnostics Ltd., Basel, Switzerland), diluted 1:30 in PBS and bovine serum albumin (BSA, Sigma, Dorset, UK) (1 mg BSA/1 ml PBS) was incubated on the tissue section for 30 minutes at room temperature, washed once in PBS then five times in deionised water to remove all traces of ions. 100 ul freshly prepared silver enhancement reagents (Roche Diagnostics Ltd., Basel, Switzerland) were applied to the immunogold-labelled slide and incubated for thirty minutes. The tissue was counter-stained with hematoxylin (Dako Ltd., Glostrup, Denmark) and images were captured by a digital camera attached to a light microscope.
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