Analysis of gene expression on human viral nephropathy after renal transplantation
| Project/Area Number |
17591696
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Urology
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| Research Institution | Osaka City Univetsity |
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Principal Investigator |
UCHIDA Junji Osaka city university, graduate school of medicine, lecturer, 大学院医学研究科, 講師 (40343412)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2005: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | cytomegaloviral nephropathy / cDNA microarray / DNA tip / Renal transplantation / Chronic allograft nephropathy / renal transplantation / BK virus / cDNA microarray / cytomegalovirus / chronicallograft nephropathy / laser-capture microdissection |
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| Research Abstract |
To diagnose acute rejection induced chronic allograft nephropathy in the future and to judge the efficacy of treatment for rejection is often difficult. It is expected to detect the specific marker for acute rejection. We used DNA microarrays in a systematic study of gene-expression profile in tubulointerstitunum obtained by laser-captured microdissection in frozen biopsy samples from patients with acute rejection.
Biopsy samples from patients with acute rejection (n=3) and control (n=3) were embedded in Tissue Tek OCT medium and snap-frozen. The cryostat section (8 u m) were made, and tubulointestinum was laser microdissected with LM-2, Arcturus Engineering. Total RNA was extracted from dissected tissues. RNA was amplified by a T7 RNA polymerase-mediated RNA amplification reaction combined with an adaptor ligation-mediated PCR (TALPAT method). After biotinylated cRNAs were fragmented, they were hybridized to the DNA tip (Human genome U133 Plus 2.0 array: 54675 genes) and signal intensity was measured by Affymetrix gene Tip system. Data analysis was performed with Gene Spring. After eliminating data showing mismatch hybridization with negligible expression in both acute rejection and control group, 18356 genes were detected. Two hundred fifty three genes were twice or more differences in expression between acute rejection group and control group. We exploited gene tip technology to identify genes expression in the specific region where acute rejection occurred by biopsy samples from patients with acute rejection.
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Report
(3 results)
Research Products
(15 results)
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[Journal Article] Molecular mechanisms and therapeutic strategies of chronic renal injury : the role of nuclear factor kappaB activation in the development of renal fibrosis.2006
Author(s)
Tamoda S, Asai T, Kuwabara N, Iwai T, Uchida J, Teramoto K, Kaneda N, Yukimura T, Komiya T, Nakatani T, Miura K.
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Journal Title
J Pharmacol Sci. 100・1
Pages: 17-21
Description
「研究成果報告書概要(和文)」より
Related Report
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[Journal Article] Molecular mechanisms and therapeutic strategies of chronic renal injury : the role of nuclear factor kappaB activati on in the development of renal fibrosis.2006
Author(s)
Tamada S, Asai T, Kuwabara N, Iwai T, Uchida J, Teramoto K, Kaneda N, Yukimura T, Komiya T, Nakatani T, Miura K.
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Journal Title
J Pharmacol Sci 100-1
Pages: 17-21
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Molecular mechanisms and therapeutic strategies of chronic renal injury : the role of nuclear factor kappa B activation in the development of renal fibrosis.2006
Author(s)
Tamada S, Asai T, Kuwabara N, Iwai T, Uchida J, Teramoto K, Kaneda N, Yukimura T, Komiya T, Nakatani T, Miura K.
-
Journal Title
J Pharmacol Sci. 100・1
Pages: 17-21
Related Report
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