Suppr超能文献

收缩性激动剂在血管平滑肌细胞生长调节中的作用。

Role of contractile agonists in growth regulation of vascular smooth muscle cells.

作者信息

Owens G K

机构信息

Department of Physiology, University of Virginia School of Medicine, Charlottesville 22908.

出版信息

Adv Exp Med Biol. 1991;308:71-9. doi: 10.1007/978-1-4684-6015-5_6.

Abstract

There is now clear evidence demonstrating that contractile agonists such as angiotensin II and arginine vasopressin are potent hypertrophic agents for cultured vascular smooth muscle cells. Furthermore, there is circumstantial evidence supporting a role for these factors in mediation of smooth muscle cell hypertrophy in hypertensive animal models as well as in maintenance of contractile mass in normotensive animals. At least part of the hypertrophic effect of angiotensin II and arginine vasopressin appears to involve a generalized increase in protein synthesis since the synthesis of most if not all proteins is increased to some extent. However, in addition, these agonists also stimulate large selective increases in the synthesis and content of a number of cytoskeletal and smooth muscle cell specific contractile proteins, including smooth muscle alpha-actin. The latter result is quite exciting since it suggests that contractile agonists may play an important role in regulation of developmental growth and differentiation of vascular smooth muscle as well as in modulating the contractile mass of smooth muscle tissues in accordance with functional demands. Observations that agonists increase expression of smooth muscle alpha-actin mRNA show that hypertrophy is not regulated solely at the translational level, although it remains to be determined whether changes are mediated transcriptionally and/or post-transcriptionally. In any event, further examination of the mechanisms whereby contractile agonists alter expression of these proteins should provide important insight regarding how these factors act as hypertrophic agents.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

目前有明确证据表明,血管紧张素II和精氨酸加压素等收缩性激动剂是培养的血管平滑肌细胞的强效肥大因子。此外,有间接证据支持这些因子在高血压动物模型中平滑肌细胞肥大的介导作用以及在正常血压动物中收缩物质维持方面的作用。血管紧张素II和精氨酸加压素的肥大效应至少部分似乎涉及蛋白质合成的普遍增加,因为大多数(如果不是全部)蛋白质的合成在某种程度上都有所增加。然而,此外,这些激动剂还能刺激多种细胞骨架和平滑肌细胞特异性收缩蛋白(包括平滑肌α-肌动蛋白)的合成和含量大幅选择性增加。后一结果相当令人兴奋,因为这表明收缩性激动剂可能在血管平滑肌的发育生长和分化调节中以及根据功能需求调节平滑肌组织的收缩物质方面发挥重要作用。激动剂增加平滑肌α-肌动蛋白mRNA表达的观察结果表明,肥大并非仅在翻译水平受到调节,尽管仍有待确定这些变化是通过转录和/或转录后介导的。无论如何,进一步研究收缩性激动剂改变这些蛋白质表达的机制应能为这些因子如何作为肥大因子发挥作用提供重要见解。(摘要截短于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验