PROLIFERATION INVIVO AND IN CULTURE OF DIFFERENTIATED ADULT ATRIAL CARDIOMYOCYTES FROM TRANSGENIC MICE

被引:113
作者
STEINHELPER, ME
LANSON, NA
DRESDNER, KP
DELCARPIO, JB
WIT, AL
CLAYCOMB, WC
FIELD, LJ
机构
[1] COLD SPRING HARBOR LAB, COLD SPRING HARBOR, NY 11724 USA
[2] COLUMBIA UNIV COLL PHYS & SURG, DEPT PHARMACOL, NEW YORK, NY 10032 USA
[3] LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT BIOCHEM & MOLEC BIOL, NEW ORLEANS, LA 70112 USA
[4] LOUISIANA STATE UNIV, MED CTR, SCH MED, DEPT ANAT, NEW ORLEANS, LA 70112 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1990年 / 259卷 / 06期
关键词
HEART TUMORS; SV40; T-ANTIGEN; CARDIAC MUSCLE CELLS; CELL CULTURE;
D O I
10.1152/ajpheart.1990.259.6.H1826
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Transgenic mice expressing atrial natriuretic factor-SV40 T-antigen fusion genes (ANF-TAG) developed unilateral right atrial tumors composed of differentiated dividing cardiomyocytes. The atrial tumors could be propagated as transplantable tumor lineages in syngeneic animals. Cardiomyocytes derived from ANF-TAG atrial tumors did not proliferate in tissue culture. However, cardiomyocytes derived from the transplantable tumor lines proliferated in culture, and these proliferating cardiomyocytes could be passaged in culture and recovered from frozen stocks. Cardiomyocytes from either tumor source were highly differentiated as determined by diverse functional and structural criteria. The cells continued to express numerous cardiac-specific proteins and retained ultra-structural features characteristic of cardiomyocytes including well-formed myofibrils, transverse tubules, and intercalated disks. In addition, the cultured cells displayed spontaneous electrical and contractile activities. These atrial tumor cardiomyocytes are a novel experimental resource for the identification of genes regulating the cardiomyocyte cell cycle.
引用
收藏
页码:H1826 / H1834
页数:9
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