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

Role and gene transfer of Intercellular signal transduction (gap junction)

Research Project

Project/Area Number 10671244
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Thoracic surgery
Research InstitutionTokyo Medical and Dental University

Principal Investigator

WATANABE Masazumi  Tokyo Medical and Dental Univ. Faculty of Medicine, Research Associate, 助手 (10282758)

Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥3,100,000 (Direct Cost: ¥3,100,000)
Fiscal Year 1999: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1998: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsGap junction / connexin 43 / gene transfer / adenovirous vector / p16 / EIE3欠損型アデノウィルス5型 / 肥大抑制 / gap junction / 加齢 / 心筋
Research Abstract

1) Gap junctions are composed of narrow membrane channels that serve as conduits for direct cell-to cell transfer of small molecules and ions. Intercellular communication via these gap junctional channels have been proposed to contribute to diverse physiological processes including tissue homeostasis, growth regulation and development. We therefore examined the aged-related changes in the rat hearts.
Methods and Results : Connexin 43, myocardial gap junction protein, was investigated in four groups (6, 30 weeks and 20, 30 months : n=6/group) by quantitative immuno-histochemical localization and electron microscopic study. Quantification of immuno-histochemical localization and westernblotting showed that obvious differences in the number and pattern of connexin 43 bands were noticed between 6, 30 weeks and 20, 30 months.
Conclusion : These age-related changes will need to be included as a potentially important factor for the incidence of arrthythmias and the mechanical, chemical distribu … More tion in the aged heart.
2) In the present study, we have assessed the efficiency and stability of gene transfer in the rat heart by the novel method.
Methods and Results : The E1E3-deleted adenovirous containing coding sequences of β-galactosidase, (AxCALacZ) were used in this experiment. 10-week-old SD male rats were anesthetized, intubated, and mechanically ventilated. Ascending aorta and pulmonary artery were snared. A 24-gage needle was placed in the ascending aorta through the apex. AxCALacZ (4x10ィイD110ィエD1pfu/ml) in a volume of 100 μL was injected with the clamping the ascending aorta and pulmonary artery for 10 seconds. After 24 hours and 2 weeks of operation, the hearts were resected and stained for LacZ. Western blotting was also done. Gross observation revealed that apparent histochemical expression of β-galactosidase in more than 90% of the area of LV of the heart was detected at 24 hours and 2 weeks after injection.
Conclusion : We have succeeded in establishing an efficient and stable gene transfer method into the heart by adenovirous vectors in rats. This method may provide an effective and useful tool for research and therapy of heart diseases. Less

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report

URL: 

Published: 1998-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi