• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

MEMBRANE-BINDING COMPLEMENT REGULATORY FACTER IN GASTROINTESTINAL TRACT

Research Project

Project/Area Number 08670607
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Gastroenterology
Research InstitutionNAGOYA CITY UNIVERSITY

Principal Investigator

JOH Takashi  NAGOYA CITY UNIVERSITY.FIRST DEPARTMENT OF INTERNAL MEDICINE.ASSISTANT PROFESSOR, 医学部, 講師 (30231369)

Co-Investigator(Kenkyū-buntansha) ITOH Makoto  NAGOYA CITY UNIVERSITY.FIRST DEPARTMENT OF INTERNAL MEDICINE.PROFESSOR, 医学部, 教授 (00080119)
OKADA Noriko  NAGOYA CITY UNIVERSITY.FIRST DEPARTMENT OF INTERNAL MEDICINE.RESEACH ASSOCIATE, 医学部, 助手 (20160682)
Project Period (FY) 1996 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1997: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1996: ¥1,000,000 (Direct Cost: ¥1,000,000)
KeywordsCOMPLEMENT / COMPLEMENT REGULATORY PROTEIN / MUCOSAL INJURY / MUCOSAL IMMUNITY / DAF / 粘膜障害
Research Abstract

In this study, complement and its regulatory system were investigated in the rat, human, and guinea pig gastrointestinal tract. Roles of complement and plasma carboxypeptidase (CP ; inactivator of C3a and C5a) in systemic shock following intestinal ischemia were studied using cobra venom factor (CVF,which reduced serum complement to undetectable level) and/or CP inhibitor. Pretreatment with CVF prevented, but CP inhibitor aggravated such a shock. In human gastric mucosa, DAF (membrane binding inhibitor of complement) was found to be unregulated during gastritis. The study on guinea pig gastric mucosa clearly demonstrated alternation in the expression of DAF gene and protein after gastric I/R.Expression of DAF mRNA was constitutively demonstrated in normal guinea pig gastric mucosa and was most intense in 6hr after I/R.However, it was detected at normal levels at 24 hr, 3 and 7 days. Expression of DAF protein was not significant from 0 to 12 hr after I/R but it was increased in amount at 24 hr and 3 days, returning to less than significant levels at 7 days. Expression of DAF isoform mRNA was also assessed by RT-PCR with specific primers for 6 isoforms (transmembrane types ; TM-a, TM-ab, TM-abc, and glycosylphosphatidyl-inositol anchored types ; GPI-a, GPI-ab, GPI-abc) were evaluated. Messenger RNAs for GPI-a, GPI-ab, GPI-abc, TM-a and TM-ab were constitutively detected in normal guinea pig gastric mucosa, whereas mRNA for TM-abc was not. However, 6 hr after I/R,mRNAs for TM-abc became detectable, with TM-a and TM-ab the dominant species. We also evaluated role of complement in a rat model for ischemia-induced gastric mucosal injury. Pretreatments with CVF and K-76 COOH,a inhibiter of complement action, significantly attenuated mucosal injury observed after reperfusion.
These findings support that complement and its regulatory system may play a significant role in pathology of gastrointestinal tract.

Report

(3 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Masahiro Ikai Makoto Itoh Takashi Joh etal: "Complement plays an essential role in systemic shock following intestinal ischemia in rats" Clin.Exp.Immunol. 106. 156-159 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Takashi Joh etal: "Complement and Gastrointestinal Ischemia" Molecular Bioligical Approch to Peptic Ulcer Disease. 31-34 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] 城 卓志 大島 忠之 猪飼 昌弘 etal: "消化性潰瘍における補体の関与" 消化器科. 24. 392-398 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] 佐々木 誠人, 城 卓志 横山 善文 etal: "ヒト胃粘膜上皮細胞におけるDAFの発現 炎症の程度およびHelicobacter pyloriとの関連について" Progress in Medicine. 17. 599-602 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Masahiro Ikai, Makoto Itoh, Takashi Joh, Yoshifumi Yokoyama, Noriko Okada, Hidechika Okada.: "Complement plays an essential role in systemic shock following intestinal ischemia in rats." Clin.Exp.Immunol.106. 156-159 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Takashi Joh: Complement and Gastrointestinal Ischemia.Molecular Biological Approach to Peptic Ulcer Disease. Gastric cell damage and repair. Akira Terano, Masaki Kitajima, Sander Szabo Edited by Axl Springer Japan Publishing Inc Yamanouchi Pharmaceutical Co., Ltd.Tokyo, 31-34 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Masahiro Ikai, Makoto Itoh, Takashi Joh, Yoshifumi Yokoyama Noriko Okada Iidechila Ckada: "Complement plays an essential role in systemic shook following intestinal is ohemia in rats" Clin Exp Immunol. 106. 156-159 (1996)

    • Related Report
      1996 Annual Research Report

URL: 

Published: 1996-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi