大鼠肾上腺髓质内皮细胞细胞外基质重塑及MMP-2活化的调控。

E. Papadimitriou, C. R. Waters, V. Manolopoulos, B. Unsworth, M. Maragoudakis, P. L. Lelkes
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引用次数: 10

摘要

我们之前报道过,将培养的大鼠肾上腺髓质内皮细胞(RAMEC)短期暴露于凝血酶会增强细胞外基质(ECM)蛋白纤维连接蛋白、层粘连蛋白和I型胶原(C-I)和IV型胶原(C-IV)的内皮下沉积(Papadimitriou等)。, 1997)。在这项工作中,我们扩展了之前对影响ECM蛋白沉积的因素的研究,包括激活或抑制一些最常见的细胞内信号的药物,如cAMP、蛋白激酶C (PKC)和钙。此外,我们还研究了观察到的ECM蛋白沉积变化与基质金属蛋白酶-2 (MMP-2)分泌之间的可能联系。福斯克林(腺苷酸环化酶激活剂)引起所研究的所有四种ECM蛋白沉积的剂量依赖性增加。异丙肾上腺素(β -肾上腺素能受体激动剂)和膜渗透cAMP类似物二丁基cAMP在低浓度下显著增加ECM蛋白的沉积量,在两种药物浓度较高时,这种增加被逆转。所有这些药物对MMP-2的分泌都有相反的作用,在减少ECM蛋白沉积的剂量下增加MMP-2的分泌,反之亦然。然而,磷酸二酯酶抑制剂IBMX升高cAMP对所研究的任何ECM蛋白的沉积量和MMP-2的分泌都没有影响。磷酸酯(PMA)激活PKC导致ECM蛋白沉积减少,MMP-2分泌增加。最后,细胞间钙与BAPTA-AM的螯合作用导致ECM沉积增加,MMP-2分泌减少。我们的研究结果表明camp -动员剂对ECM蛋白沉积的调节模式很复杂,并且ECM蛋白沉积与MMP-2分泌呈负相关。这两个过程的协调调节对新血管的形成和血管壁的完整性是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of extracellular matrix remodeling and MMP-2 activation in cultured rat adrenal medullary endothelial cells.
We previously reported that short term exposure of cultured rat adrenal medullary endothelial cells (RAMEC) to thrombin enhances the subendothelial deposition of extracellular matrix (ECM) proteins fibronectin, laminin, and collagen types I (C-I) and IV (C-IV) (Papadimitriou et at., 1997). In this work, we extended our previous studies on factors that affect ECM protein deposition to include agents that activate or inhibit some of the most common intracellular signals such as cAMP, protein kinase C (PKC) and calcium. Furthemore, we investigated the possible link between the observed alterations in ECM protein deposition and the secretion of matrix metalloproteinase-2 (MMP-2). Forskolin (adenylyl cyclase activator) caused a dose-dependent increase in the deposition of all four ECM proteins studied. Isoproterenol (beta-adrenergic receptor agonist) and the membrane-permeant cAMP analogue dibutyryl-cAMP, significantly increased the deposited amounts of ECM proteins at low concentrations, and this increase was reversed at higher concentrations of both agents. All these agents had the opposite effect on MMP-2 secretion, increasing it at doses where they decreased ECM protein deposition and vice-versa. However, elevation of cAMP by the phosphodiesterase inhibitor IBMX had no effect neither on the deposited amounts of any of the ECM proteins studied nor on MMP-2 secretion. Activation of PKC by phorbol ester (PMA) resulted in a decrease in ECM protein deposition and an increase in MMP-2 secretion. Finally, chelation of intercellular calcium with BAPTA-AM resulted in an increased ECM deposition and a decrease in MMP-2 secretion, Our results show a complex pattern of regulation of ECM protein deposition by cAMP-mobilizing agents, and also indicate an inverse correlation between ECM protein deposition and secretion of MMP-2. The concerted regulation of both these processes is essential in the formation of new blood vessels and for the integrity of the vascular wall.
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