Differential protection of primary rat cardiocytes by transfection of specific heat stress proteins

被引:59
作者
Cumming, DVE
Heads, RJ
Watson, A
Latchman, DS
Yellon, DM
机构
[1] UCL HOSP, HATTER INST CARDIOVASC STUDIES, DEPT ACAD CARDIOL, LONDON WC1E 6DB, ENGLAND
[2] UCL, SCH MED, DEPT MOL PATHOL, MED MOL BIOL UNIT, LONDON W1P 6DB, ENGLAND
基金
英国惠康基金;
关键词
heat stress; ischaemia; cardiac myocytes; stress proteins;
D O I
10.1006/jmcc.1996.0227
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to examine the individual contribution of specific heat stress proteins in primary rat cardiocytes to any protection observed following lethal heat stress or simulated lethal ischaemia. cDNAs for the inducible heat stress protein 70, for heat stress proteins 90 or 60, or a control plasmid were cotransfected with a detectable marker, alkaline phosphatase, into cardiocytes. Survival assays were performed after the lethal stress. Transfection of the inducible heat stress protein 70 was found to increase survival following a lethal heat stress by 2.45-fold (P<0.01) and against lethal ischaemia by 2.71-fold (P<0.01). Transfection of heat stress protein 90 improved survival against heat by 2.55-fold (P<0.05) but failed to have any effect on survival against lethal ischaemia, Transfection of heat stress protein 60 offered no protection against either stress. (C) 1996 Academic Press Limited
引用
收藏
页码:2343 / 2349
页数:7
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