IDENTIFICATION OF SV40 LARGE T-ANTIGEN-ASSOCIATED PROTEINS IN CARDIOMYOCYTES FROM TRANSGENIC MICE

被引:37
作者
DAUD, AI
LANSON, NA
CLAYCOMB, WC
FIELD, LJ
机构
[1] INDIANA UNIV, SCH MED, KRANNERT INST CARDIOL, 1111 W 10TH ST, INDIANAPOLIS, IN 46202 USA
[2] LOUISIANA STATE UNIV, MED CTR, DEPT BIOCHEM, NEW ORLEANS, LA 70112 USA
[3] LOUISIANA STATE UNIV, MED CTR, DEPT MOLEC BIOL, NEW ORLEANS, LA 70112 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 264卷 / 05期
关键词
CARDIOMYOCYTE GROWTH; CARDIAC TUMORIGENESIS;
D O I
10.1152/ajpheart.1993.264.5.H1693
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A cell line derived from transgenic mice expressing the SV40 large T-antigen oncogene in the heart was used to identify cardiomyocyte targets for T-antigen binding. A novel protein of molecular mass of 193 kDa was identified as an associated protein by virtue of its ability to be co-immunoprecipitated with multiple anti-T-antigen antibodies. Two previously described proteins, p120 and p53, were also observed to complex with T-antigen in transformed cardiomyocytes. In addition, several proteins that cross-reacted with either anti-T-antigen or anti-p53 antibodies were identified. Two of these proteins, of apparent molecular masses of 250 and 110 kDa, were only observed in cardiomyocytes. Expression of a third cross-reacting protein of a molecular mass of 180 kDa appeared to be dependent on the growth status of the cells. These proteins may be important constituents of the cardiomyocyte cell cycle, as well as potential cellular targets for myocardial regeneration.
引用
收藏
页码:H1693 / H1700
页数:8
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