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首页> 外文期刊>Archives of Biochemistry and Biophysics >Differential regulation of endothelin secretion and endothelin receptor mRNA levels in JAR, JEG-3, and BeWo choriocarcinoma cell lines and in human trophoblasts, their nonmalignant counterpart
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Differential regulation of endothelin secretion and endothelin receptor mRNA levels in JAR, JEG-3, and BeWo choriocarcinoma cell lines and in human trophoblasts, their nonmalignant counterpart

机译:在JAR,JEG-3和BeWo绒毛膜癌细胞和人类滋养细胞(非恶性对应物)中内皮素分泌和内皮素受体mRNA水平的差异调节

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摘要

Endothelin (ET) secretion and expression of both ET-A and ET-B receptor subtypes have been found in a number of primary cancers. The present study tested (1) whether choriocarcinoma cells and their nonmalignant counterpart, the trophoblast, secrete ET-1 and express ET-A and ET-B receptors; (2) whether ET-1 secretion and receptor mRNA levels are regulated by the same factors in nonvascular tissues as in vascular tissues; and (3) whether such regulation is similar in malignant and nonmalignant cells. All cells secreted ET-1 in similar amounts (similar to0.8 fmol/10(6) cells per 24 h) and secretion was unaffected by culture and treatment. Whereas ET-B accounted for almost all (>98%) ET receptor transcripts in the choriocarcinoma cells, the trophoblasts expressed about 20% ET-A receptor mRNA. During control cultures, ET-B mRNA levels rose in choriocarcinoma, with the greatest relative increase (6-fold; P < 0.05 vs 9 h) in BeWo, whereas in trophoblasts, ET-A mRNA transiently changed after 24 and 48 h, Treatment with dexamethasone and glucose did not alter the mRNA levels in all cells. Insulin induced changes (P < 0.05) in ET-B mRNA levels in BeWo (+90 and +60% after 24 and 48 h, respectively) and JEG-3 (-70%), but not in JAR and trophoblast cells. We conclude that malignant transformation affects the responsiveness of the endothelin receptor system to external stimuli and that the regulation of the endothelin system differs in vascular and nonvascular tissues. (C) 2000 Academic Press. [References: 43]
机译:内皮素(ET)的分泌以及ET-A和ET-B受体亚型的表达已在许多原发性癌症中发现。本研究测试(1)绒毛膜癌细胞及其非恶性对应物滋养层是否分泌ET-1并表达ET-A和ET-B受体; (2)非血管组织中与血管组织中ET-1的分泌和受体mRNA水平是否受到相同因素的调节; (3)这种调节在恶性和非恶性细胞中是否相似。所有细胞以相似的量分泌ET-1(类似于每24小时0.8 fmol / 10(6)个细胞),并且其分泌不受培养和处理的影响。 ET-B占绒癌细胞中几乎所有(> 98%)ET受体转录物,而滋养细胞表达约20%ET-A受体mRNA。在对照培养过程中,绒毛膜癌中ET-B mRNA的水平上升,在BeWo中相对增加最大(6倍; P <0.05 vs 9 h),而在滋养细胞中,ET-A mRNA在24和48 h后瞬时改变地塞米松和葡萄糖联合使用不会改变所有细胞中的mRNA水平。胰岛素诱导BeWo(分别在24和48 h后分别增加90和+ 60%)和JEG-3(-70%)中ET-B mRNA水平的变化(P <0.05),但在JAR和滋养细胞中则没有。我们得出的结论是,恶性转化会影响内皮素受体系统对外部刺激的反应,并且内皮素系统的调节在血管组织和非血管组织中均不同。 (C)2000年学术出版社。 [参考:43]

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