|Year : 2004 | Volume
| Issue : 3 | Page : 167-170
A semi-quantitative method for the estimation of adenosine A1 receptor mRNA levels in rat kidney
Department of Pharmacology, Medical Faculty, Çukurova University, 01330, Adana, Turkey
Department of Pharmacology, Medical Faculty, Çukurova University, 01330, Adana, Turkey
OBJECTIVE: To develop Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) method for the estimation of adenosine A1 receptor mRNA levels in rat kidney. MATERIAL AND METHODS: Total cellular RNA was isolated from whole rat kidney by small-scale total RNA preparation protocol and it was reverse transcribed into cDNA. The cDNA was subjected to PCR amplification using gen specific primers. The amplified cDNA was evaluated by gel electrophoresis and the intensity of the bands were visualized and quantitated with a FujiBAS 1000 PhosphorImager. Then the adenosine A1 receptor mRNA levels were extrapolated from the standard curve. RESULTS: Adenosine A1 receptor mRNA levels in rat kidney were measured as: 1.30 ± 0.17 X 107 copies of adenosine A1 receptor transcript/mg total RNA. CONCLUSION: The RT-PCR method developed for the estimation of adenosine A1 receptor mRNA levels in rat kidney is sensitive and reliable.
|How to cite this article:|
Dondas N. A semi-quantitative method for the estimation of adenosine A1 receptor mRNA levels in rat kidney. Indian J Pharmacol 2004;36:167-70
|How to cite this URL:|
Dondas N. A semi-quantitative method for the estimation of adenosine A1 receptor mRNA levels in rat kidney. Indian J Pharmacol [serial online] 2004 [cited 2021 Jun 21];36:167-70. Available from: https://www.ijp-online.com/text.asp?2004/36/3/167/6872
| » Introduction|| |
Adenosine is an endogenous nucleoside that modulates many physiological processes via its receptors including A1, A2a, A2b and A3. However, a functional role has especially been ascribed to A1 receptors in the kidney. Therefore, adenosine A1 receptors are extensively characterized in this tissue. But a sensitive method for the estimation of the mRNA levels of these receptors is still quite important, since the common methods including in situ hybridization, northern blot and slot blot analysis are no longer practical. In the present study, an attempt has been made to develop a sensitive RT-PCR method for the detection of adenosine A1 receptor mRNA levels in rat kidney.
| » Material and Methods|| |
Male Wistar rats (200-250 g) were housed in polypropylene cages in controlled temperature (27±20C) and light. They were fed standard rat pellets. Food and water were provided ad libitum. The care and use of animals was carried out according to the Code of Practice set out by the (UK) Animals (Scientific Procedures) Act 1986.
Small-scale total RNA isolation for the extraction and purification of total cellular RNA from whole rat kidney: 1) Male Wistar rats (200-250 g) were anesthetized with sodium thiobutabarbitone (180 mg/kg-1, i.p.) and were killed by a blow to the head followed by exsanguination. Kidneys were removed and immediately freeze-clamped in liquid nitrogen and then stored at -700C until required. 2) The kidney was homogenized in 10 ml of ice-cold denaturing solution (0.5 g/ml guanidium thiocyanate) with a Polytron homogeniser (2x15 second bursts). 3) 1.0 ml sodium acetate (2 M, pH 4.0) was added with mixing. 4) Five ml citrate-buffered phenol (pH 4.0) and 5 ml Chloroform-isoamyl alcohol (48:2 v/v) mix were added, mixed and chilled on ice for 15 min. 5) The mixture was then transferred to an eppendorf tube (1.5 ml) and centrifuged (13 krpm, 10 min), then the top aqueous phase was pipetted into a fresh tube. After the addition of an equal volume (10 ml) of isopropanol, the mixture was chilled at -200C for 30 min. 6) The total cellular RNA was pelleted by centrifugation (13 krpm, 10 min). Then the supernatant was decanted and the pellet dried by inversion on a paper towel and it was resuspended in 500 ml denaturing solution with a brief heating at 650C. 7) Total cellular RNA was again precipitated with 500 ml isopropanol and centrifugated (13 krpm, 10 min), then it was washed with 500 ml of ice-cold ethanol (70%) and re-centrifugated (13 krpm, 10 min). The pellet was dried at 370C for 15 min and dissolved in 50 ml of DEPC (diethyl pyrocarbonate)-treated water with brief heating to 650C to aid solubilisation. The resulting total cellular RNA was stored at -700C.
Reverse transcriptase polymerase chain reaction (RT-PCR)
a) Reverse transcription (RT)
The concentration of total cellular RNA, isolated from whole rat kidney, was adjusted by UV spectrophotometry to 1 mg.ml-1 in diethylpyrocarbonate-treated water. Then 2.0 ml of total RNA (1mg/ml) and 1.0 ml of oligo (dT)12-18 primer (0.2 mg/ml) were added into a DEPC-treated eppendorf tube and heated at 650C for 3 min and then the tube was cooled slowly to room temperature. After that 2 ml of DTT (dithiothreitol; 0.1M), 4 ml of 5x first strand buffer (250 mM Tris.Cl (pH 8.3), 375 mM KCl and 15 mM MgCl2), 1 ml of dNTPs (deoxynucleoside triphosphates; 10 mM), 9 ml of RNA grade H2O and 1 ml of Murine leukemia virus reverse transcriptase (MMLV RT; 200 U/ml) were added, mixed, and kept at 370C for 15 min. Then the eppendorf tube was heated to 950C for 3 min (to terminate the reaction and denature the mRNA). And then 5 ml of aliquot was taken and used as a template (complementary DNA; cDNA) in PCR.
b) Polymerase chain reaction (PCR)
Into a small eppendorf tube 5 ml of RT-template (cDNA), 5 ml of 10xPCR buffer (Tris.Cl [100 mM; pH 8.4], 0.5 M KCl, 1% Triton X-100), 4 ml MgCl2 (25 mM), 1 ml of dNTPs (deoxynucleoside triphosphates; 2 mM ), 1 ml of N-terminus primer (5'-3'; 500 pmol), 1 ml of C-terminus primer (5'-3'; 500 pmol) (primer sequences were given in [Table - 1], 1ml of a-[32P]-dCTP (2'-deoxycytidine-5'-triphosphate; 50 mCi, spec. act. 3000 Ci.mmol- and 31 ml of MilliQ H2O were added and mixed. Then 50 ml of mineral oil was added. After heating to 950C for a few minutes, 1 ml of Taq (Thermophilus aquaticus) DNA polymerase (125 units) prepared according to the method of Pluthers (1993), was added (The PCR protocol for adenosine A1 receptors and b-actin are given in [Table - 2].
After thermocycling, 10 ml of PCR product was subjected to agarose gel (1% agarose gel and 0.1 mM ethidium bromide) electrophoresis [Figure - 1] and [Figure:2]. To visualize the PCR product, the gel was dried overnight by sandwiching between 20-25 paper towels and applying a 1 kg weight. The dried gel was covered with cling film (Saran) and exposed to FujiBAS-IIIs imaging plate for 2 h prior to visualization on the FujiBAS 1000 bio-imaging analyzer. Then it was visualized and the intensity of the bands were quantitated.
Preparation and purification of cRNAs of adenosine
A1 receptors and b-actin for the standard curve:
The cRNAs were produced by in vitro transcription of adenosine A1 receptor and b-actin cDNAs in pSPORT2 and pBluescript II, respectively, with T7 RNA polymerase-based transcription kit. The protocol: 1) In a small 0.5 ml DEPC-treated eppendorf tube, 6 ml of RNase free H2O, 2 ml of 10xBuffer, 2 ml of each nucleotide (ATP, GTP, CTP, UTP), 2 ml of template (bA or adenosine receptor cDNA; 1.0 mg/ml) and 2 ml of enzyme mix (T7 RNA polymerase and placental ribonuclease inhibitor) were added and incubated at 370C for 4 h. 2). 1 ml RNAase free DNAase was added to the reaction and was incubated at 370C for 15 min. 3). 115 ml of RNAase free H2O and 15 ml of ammonium acetate were added to the reaction. Then it was cleaned by phenol/CHCl3 extraction; 151 ml Phenol mix (Phenol:CHCl3:Isoamylalcohol; 50:48:2 v/v) was added and centrifuged (13 krpm, 5 min). The top layer was taken into a fresh eppendorf tube and 151 ml CHCl3 mix (CHCl3:Isoamylalcohol; 48:2) was added. After mixing, the aliquot was centrifuged (13 krpm, 5 min). The top layer was taken into a fresh eppendorf tube, then 20 ml of sodium acetate (3M, pH 5.2) and 151 ml isopropanol were added and kept at -200C for 30-60 min. After that the cRNA was pelleted by using a centrifuge (13 krpm, 10 min) and the supernatant was removed, then 500 ml of icecold ethanol (70%) was added. After centrifuging for 10 min at 13 krpm, ethanol was removed and the cRNA pellet was dried at 370C for 10-15 min. Then it was dissolved in 10 ml water.
Preparation of standard curve
Standard curves were generated using varying amounts (1/3, 1/9, 1/27, 1/81, 1/243) of in vitro transcribed adenosine A1 receptor and b-actin cRNAs. These serially diluted cRNAs were subjected to RT-PCR and the amount of the PCR product determined by densitometry. The band densities of the test samples were adjusted for concentration differences (dividing by the concentration in mg/ml) and then mRNA levels were extrapolated from the standard curve. To improve assay reproducibility, where numerous assays were performed at a time, a master-mix of all reagents was prepared and aliquoted to ensure that all assays received equal amounts and concentrations of substrate and reagents.
All oligonucleotide primers were obtained from Genosys Biotechnologies Ltd. Deoxyribonucleotides and oligo (dT)12-18 primer were purchased from Pharmacia. M-MLV reverse transcriptase was obtained from Gibco-BRL (Life Technologies). a-[32P] dCTP was obtained from ICN Pharmaceuticals. The Ambion mMESSAGE mMACHINE in vitro transcription kit was obtained from ams Biotechnology. MilliQ water (18 MW, Millipore) was used in the preparation of all reagents. For procedures involving RNA, all reagents and plasticware were treated with diethylpyrocarbonate (DEPC; 0.5%).
Analysis of data
mRNA levels were expressed as transcript number. Data are given as mean ± SEM and statistical comparison was made using t-test (One-Sample test). A value of P<0.05 was considered statistically significant. The intensities of the adenosine receptor mRNA bands were normalized relative to that of b-actin bands by dividing the former by the b-actin-specific PCR product densities. b-actin acted as a control for sample to sample variation in reverse transcription and PCR conditions, and the extent of degradation and recovery of RNA.
| » Results|| |
The absolute mRNA levels of adenosine A1 receptors in rat kidney were 1.30 ± 0.17 x 107 copies of adenosine A1 receptor transcript/mg total RNA. The absolute mRNA levels of b-actin in the rat kidney were 2.26 ± 0.19 X 109 copies of b-actin transcript/mg total RNA. mRNA was extracted from the kidneys of six rats. b-actin or adenosine A1 receptor mRNA levels in kidneys did not show statistically significant variations.
| » Discussion|| |
In the present study, a reverse transcriptase-polymerase chain reaction (RT-PCR) assay was developed and optimized to enable the absolute quantitation of the mRNA levels of adenosine A1 receptors. Several techniques are currently available to measure changes in gene expression including Northern blot, RNase protection assay, in situ hybridisation, and RT-PCR. The Northern blot or the more sensitive RNase protection assay is sufficient to detect quantitative differences between samples. However, if the sample quantity is low or the target message is rare these techniques are no longer practical. In the RT-PCR method, which is developed in the present study, less than 10 copies of target RNA can be estimated. This method is, actually, a semi-quantitative method.
In the present study, small-scale total RNA isolation protocol for the extraction and purification of total cellular RNA from the rat kidney was also developed. This is a slight modification of the method described by Chromoczynski and Sacchi (1987) who used a large-scale total RNA isolation procedure. This modification was attempted since the new protocol of RNA isolation could be completed in half the time of the large-scale method, conducive to the handling of a large number of samples, and it used only a fraction of the reagents whilst maintaining the quality of the total cellular RNA isolated.
In conclusion, in the present study reverse transcriptase polymerase chain reaction (RT-PCR) technique was developed and optimized to quantitate the adenosine A1 receptor mRNA levels. The precision of the method values indicates that the developed RT-PCR method for the estimation of adenosine A1 receptor mRNA levels is a very sensitive, reliable and accurate one. Such a sensitive method is essential for the determination of extremely small amounts of mRNA levels.
| » Acknowledgements|| |
I am grateful to Dr. C. J. Bowmer, Dr. A. Sivaprasadarao and Dr. M. J. Morton for their kind help.
| » References|| |
|1.||Collis MG, Hourani SM. Adenosine receptor subtypes. Trends Pharmacol Sci 1993;14:360-6. [PUBMED] |
|2.||Navar LG, Inscho EW, Majid DSA, Imig JD, Harrison-Bernard LM, Mitchell KD. Paracrine regulation of the renal microcirculation. Physiol Rev 1996;76:425-536. |
|3.||Dixon AK, Gubitz AK, Sirinathsinghji DJS, Richardson PJ, Freeman TC. Tissue distribution of adenosine receptor mRNAs in the rat. Br J Pharmacol 1996; 118:1461-8. |
|4.||Pluthero FC. Rapid purification of high activity Taq DNA polymerase. Nucleic Acids Res 1993;21:4850-1. |
|5.||Don RH, Cox PT, Wainwright BJ, Baker K, Mattick JS. 'Touchdown' PCR to circumvent spurious priming during gene amplification. Nucleic Acids Res 1991; 19:4008. [PUBMED] |
|6.||Rappolee DA, Mark D, Banda MJ, Werb Z. Wound macrophages express TGF-á and other growth factors in vivo: analysis by mRNA phenotyping. Science 1988;241:708-12. [PUBMED] |
|7.||Chromoczynski, P, Sacchi N. Single-step method for RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987;162:156-9. |