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Pathogenesis of glomerulonephritis (IgA nephropathy and FcαR)

Research Project

Project/Area Number 11671049
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Kidney internal medicine
Research InstitutionJUNTENDO UNIVERSITY

Principal Investigator

TOMINO Yasuhiko  Juntendo University School of Medicine, Professo, 医学部, 教授 (60130077)

Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 2000: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1999: ¥1,400,000 (Direct Cost: ¥1,400,000)
KeywordsIgA nephropathy / Fcα receptor / gene polymorphism promoter region / promoter region / SNP / SNP / 原発性糸球体腎炎
Research Abstract

One of the most critical findings in patients with IgA nephropathy is glomerular mesangial deposition of IgA.It is still unknown whether the activation of mesangial cells is directly triggered by IgA.FcαR is the major receptor for binding of IgA in various cells, and displays various immunological responses on binding. There is controversy as to whether FcαR is expressed on mesangial cells, although it is important to analyze the mesangial functions via FcαR in the pathogenesis of IgA nephropathy. In this time, we established mesangial transfectants which expressed FcαR and FcR γ chain, and then analyzed the biological function. We confirmed that mesangial cells had potential for cell-activation (tyrosine phosphorylation, syk activation arid MCP-1 production) with FcαR cross-linking.
These results suggested that FcαR with the FcRγ, chain may contribute to the mesangial response to IgA deposition.
Next, we have recently identified two novel polymorphisms (-114T/C and +56T/C relative to the major transcription start site) in the functional promoter region of the FcαR gene. Since altered FcαR expression may be associated with IgA nephropathy, we examined these promoter polymorphisms in this disease. The study demonstrated that the frequency of the +56C allele and CC genotype in patients with IgA nephropathy was significantly higher than that in patients with other primary glomerulonephritis and healthy adults. In contrast, no significant difference in the frequencies of the +56CC genotype and +56C allele was observed between other primary glomerulonephritis patients and healthy adults. The frequency of the 114CC genotype in patients with IgA nephropathy was also significantly increased, compared with those in both control groups. It appears that polymorphisms of the FcαR promoter region are associated with susceptibility to IgA nephropathy, suggesting the importance of the FcαR gene and its expression in this disease.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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