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Development of severe myocardial infarction with gene engineered auto cardiomyoblast

Research Project

Project/Area Number 11671303
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Thoracic surgery
Research InstitutionYAMAGATA UNIVERSITY

Principal Investigator

MINOWA Takashi  Yamagata Univ, Med, Assistant Professor, 医学部, 助手 (50292420)

Co-Investigator(Kenkyū-buntansha) WATANABE Takao  Yamagata Univ, Med, Associate Professor, 医学部, 助教授 (60138922)
INUI Kiyoshige  Yamagata Univ, Med, Assistant Professor, 医学部, 助手 (70250941)
SHIMAZAKI Yasuhisa  Yamagata Univ, Med, Professor, 医学部, 教授 (60116043)
高橋 俊樹  山形大学, 医学部, 講師 (50263257)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2000: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1999: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsGene therapy / Cell transplantation / VEGF / Myocardial infarction
Research Abstract

In this experiment, whether gene transfected cell transplanted in the organ can survive in the tissue and change the circumference organization was examined. Thoracotomy of 400g SD rat was carried out under the intratracheal intubation, and the left ventricular myocardium was cryoinjured by metallic tip cooled by liquid nitrogen. Two weeks after the injury of myocardium, thoracotomy through the same intercostal space was carried out, and 500000 VEGF cDNA transfected H9c2 cells in the 100 microlitter medium were injected in the injured myocardium. Two weeks after the cell transplantation, rats were sacrificed. Heart were fixed in the buffered formalin, paraffin embedded, sliced 5 micrometer thickness and stained by HE staining or immunohistochemical staining using anti-CD34 antibody or anti-6xHis antibody. Numerous capillaries in the damaged myocardium were recognized. And CD34 immunostaining showed that the cell in the capillaries were endothelium. Anti-6xHis immunostaining showed that the VEGF was excreted around the transplanted cells and the massive capillary formation was restricted in the positive staining area of VEGF.Our data showed that the secretory protein from the gene transfected cell transplanted by injection in the damaged myocardium could reorganize the surrounding tissue.

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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