Microvascular endothelial cells remodel cultured adult cardiomyocytes and increase their survival

被引:27
作者
Kubin, T
Ando, H
Scholz, D
Bramlage, P
Kostin, S
van Veen, A
Heling, A
Hein, S
Fischer, S
Breier, A
Schaper, J
Schaper, W
机构
[1] Max Planck Inst, Dept Expt Cardiol, D-61231 Bad Nauheim, Germany
[2] Kerckhoff Clin, D-61231 Bad Nauheim, Germany
[3] Slovak Acad Sci, Inst Mol Physiol & Genet, Bratislava 83334, Slovakia
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1999年 / 276卷 / 06期
关键词
trophic factors; growth factors; fetal marker; myocardial hypertrophy; cell culture;
D O I
10.1152/ajpheart.1999.276.6.H2179
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the paracrine effect of cardiac microvascular endothelial cells (MVEC) on cultured adult rat cardiomyocytes (ARC). ARC were exposed for 8 days to serum-free medium (CM)conditioned by MVEC. Controls were grown in FCS or FCS-free medium. Protein synthesis of CM-stimulated ARC increased twofold versus 5% FCS-stimulated cells until day 8. Seventy-nine percent of CM-treated myocytes survived, whereas only twenty-four percent of FCS-free ARC retained viability. The phenotype of myocytes exposed to CM was different from control. Analysis by confocal laser microscopy of CM-stimulated myocytes showed actin staining throughout the whole cell body up to the peripheral extensions, with concomitant appearance of myomesin in a cross-striated pattern. The reexpression of fetal a-smooth muscle actin determined immunohistochemically and by Western blot increased from day 6 in CM-treated cells, whereas ARC grown in up to 20% serum were negative. These effects could not be mimicked by any of the other cardioactive substances tested here, indicating a novel trophic factor in CM.
引用
收藏
页码:H2179 / H2187
页数:9
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