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1999 Fiscal Year Final Research Report Summary

Analysis of Signal Transduction and Application to Larger Animals of Intrathymic Tolerance Induction

Research Project

Project/Area Number 10671121
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General surgery
Research InstitutionSaga Medical School (1999)
Kyushu University (1998)

Principal Investigator

NAKAFUSA Yuji  Saga Medical School, Faculty of Medicine, Associate Professor, 医学部, 助教授 (80253417)

Co-Investigator(Kenkyū-buntansha) SUGITANI Atsushi  Kyushu University, Faculty of Medicine, Assistant Professor, 医学部, 講師 (00294934)
Project Period (FY) 1998 – 1999
Keywordstransplatation immunology / Immunological tolerance / intrathymic tolerance / thymus / cardiac transplantation / tyrosine kinase / calcineurin
Research Abstract

Background. It has been reported that donor-specific tolerance to a cardiac allograft can be achieved after thc intrathymic (IT) injection of donor splenocytes and a single intraperitoneal injection of anti-lymphocyte serum (ALS) in a fully MHC-disparate rat combination. The aim of the present study was to identify thc intracellular signaling pathways required for the induction of this tolerance.
Materials and Methods. Male Buffalo (BUF; RT1ィイD1bィエD1) rats at 6 to 8 weeks of age underwent IT injection of 25 x 10ィイD16ィエD1 Lewis (LEW ; RT1ィイD11ィエD1) splenocytes and simultaneously received an intraperitoneal injection of 1 ml ALS (day 0). To examine the intracellular signal transduction, the BUF recipients were treated with genistein (protein tyrosine kinases inhibitor, 20mg/kg/day, i.p.), tacrolimus (FK506, calcineurin inhibitor, 1mg/kg/day, s.c) or cyclosporine A (CsA, calcineurin inhibitor, 5mg/kg/day, s.c.) for 7 days from 1 day before IT injection plus ALS (day-1〜5). All BUF recipient … More s underwent transplantation with a heterotopic LEW cardiac allograft on day 21.
Results. IT injection of donor splenocytes plus ALS induced indefinite cardiac allograft survival in 90% of thc BUF recipients. Early treatment of thc BUF recipients with genistein (day -1〜5), but not delay treatment ( day7〜13 ) abrogated the induction of the tolerance. IT injection of splenocytes from genistein (20mg/kg/day, 7 days, i.p.)-treated LEW donor plus ALS resulted in indefinite survival of cardiac allografts in all recipients, indicating that genistein treatment does not interfere the signal expression on the donor splenocytes to induce tolerance. In contrast to genistein, treatment with FK506 or CsA of the recipients received IT injection plus ALS resulted in indefinite or prolonged survival of cardiac allografts. It was confirmed that genistein, FK506, or CsA did not reduce the effect of ALS on lymphocyte depletion in the thymus and periphery of BUF rats.
Conclusions. Activation of protein tyrosine kinases but not calcineurin was required for the intracellular signal transduction to induce the tolerance after intrathymic injection of donor splenocytes plus ALS. Less

  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] Roland CR et al.: "gadolinium chloride inhibits lipopolysuccharide - induced motality and in vivo prostagrandin E_2 release by splenic macrophages"Journal of gastrointestinal Surgery. 3(3). 301-307 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takeda K et al.: "Role of indirect allorecognition pathaway for prolongation of rat liver allograft survival"Transplantation Proceedings. 31. 432-433 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Roland CR.; Nakafusa Y.; Flye MW.: "Gadolinium chloride inhibits lipopolysaccharide-induced mortality and in vivo prostaglandin E2 release by splenic macrophages"Journal of Gastrointestinal Surgery. 3(3). 301-307 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takeda K.; Arima T.; Kawano R.; Ohtomo N.; Sugitani A.; Nakafusa Y.; Tanaka M.: "Role of indirect allorecognition pathway for prolongation of rat liver allograft survival"Transplantation Proceedings. 31. 432-433 (1999)

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

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Published: 2001-10-23  

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