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

2001 Fiscal Year Final Research Report Summary

Study of a novel autoantigen related to autoimmune enteropathy with renal tubular dysfunction

Research Project

Project/Area Number 12470162
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionHokkaido University

Principal Investigator

KOBAYASHI Kunihiko  Hokkaido Univ., Grad. School of Med., Prof., 大学院・医学研究科, 教授 (60091451)

Co-Investigator(Kenkyū-buntansha) KOBAYASHI Ichiro  Hokkaido University Medical Hospital, Physician, 医学部・附属病院, 医員
SASAKI Satoshi  Hokkaido University, Graduate School of Medical, Instructor, 大学院・医学研究科, 助手 (70312345)
OKANO Motohiko  Hokkaido University Medical Hospital, Lec., 医学部・附属病院, 講師 (50261300)
Project Period (FY) 2000 – 2001
Keywordsautoimume enteropathy / intractable diarrhea / AIE-75 / Usher syndrome / autoantigen
Research Abstract

Autoimmune enteropathy is a rare desease characterized by circulating autoantibody against epithelial cells of the intestine. Some cases are inherited by an X-linked manner and named immunedysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX). The aim of our study is to identity the target of the autoantibody and to clarify the biological functions of the antigen.
For this purpose, we screened λgt11 cDNA expression library from human duodenum with the serum from an IPEX patient, and identified a cDNA encoding a novel protein consisting of 552 amino acids. The protein named autoimmune, enteropathy-related 75 kDa antigen (AIE-75) predominantly distributed to the brush border in the small intestine and proximal renal tubulus. AIE-75 gene was mapped to chromosome 11p14.3. In collaboration with C. Petit of the Pasteur Institute, we demonstrated that AIE-75 also distributed to the epithelial cells in the inner ear and that mutation of the gene caused a hereditary deafness, Usher syndrome type 1C. This suggests that AIE-75 plays a biologically significant rolls in not only the small intestine and kidney but also in the inner ear.
AIE-75 contains three PDZ domains, suggesting that the protein functions as a linker protein. Using yeast two-hybrid screening, we identified a novel protein homologous to a tumor suppressor, MCC, and named MCC-2. In addition, overexpression of AIE-75 in a colon cancer cell line, SW480, which lacks AIE-75 resulted in G2/M arrest. These findings suggest that AIE-75 is involved in the regulation of cell cycle. Recently, a forkhead/winged helix transcription regulator, FOXP3, has been identified as a causative gene of IPEX. We reported two novel mutation of FOXP3 in Japanese patients with IPEX and suggested that Ile363 is necessary for the normal function of FOXP3.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Kobayashi I, Imamura K, et al.: "A 75-κD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathy"Clin.Exp.Immunol.. 111巻. 527-531 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kobayashi I, Imamura K, et al.: "Identification of an autoimmune enteropathy-related 75-kilodalton antigen"Gastroenterology. 117巻. 823-830 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Verpy E, Leibovici, M, et al.: "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C"Nature Genetics. 26巻. 51-56 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishikawa S, Kobayashi I, et al.: "Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain protein AIE-75"Gene. 276巻. 101-110 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kobayashi I, Shiari R, et al.: "Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome"J.Med.Genet. 38巻. 874-876 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kobayashi I, Kawamura N, et al.: "A long-term survivor with the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome"N.Engl.J.Med. 345巻. 999-1000 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kobayashi I, Imamura K, Yamada M, Okano M, Yara, A., Ikema S, Ishikawa N, Kobayashi K, Sakiyama Y: "A 75-kD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathy."Clin. Exp. Immunol.. 111. 527-531 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kobayashi I, Imamura K, Kubota M, Ishikawa S, Yamada M, Tonoki H, Okano M, Storch WB, Moriuchi T, Sakiyama Y, Kobayashi, K: "Identification of an autoimmune enteropathy-related 75-kilodalton antigen."Gastroenterology. 117. 823-830 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Verpy E, Leibovici, M, Zwaenepoel I, Liu X-Z, Gal A, Salem N, Mansour A, Blanchard S, Kobayashi I, Keats BJ B, Slim R, Petit C.: "A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C."Nature Genetics. 26. 51-56 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ishikawa S, Kobayashi I, Hamada J, Tada M, Hirai A, Furuuchi K, Takahashi Y, Ba Y, Moriuchi, T.: "Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain protein AIE-75."Gene.. 267. 101-110 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kobavashi I, Shiari R, Yamada M, Kawamura N, Okano M, Yara A, Iguchi A, Ishikawa N, Ariga T, Sakiyama Y, Ochs HD, Kobayashi K.: "Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome."J. Med. Genet.. 38. 874-876 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kobayashi I, Kawamura N, Okano M.: "A long-term survivor with the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome."N. Engl. J. Med.. 345. 999-1000 (2001)

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 2003-09-17  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi