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星形胶质细胞中的过程形成:细胞骨架蛋白的调节

Process formation in astrocytes: modulation of cytoskeletal proteins.

作者信息

Padmanabhan J, Shelanski M L

机构信息

Department of Pathology, Taub Center for Alzheimer's Disease Research, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.

出版信息

Neurochem Res. 1998 Mar;23(3):377-84. doi: 10.1023/a:1022413718447.

Abstract

Studies on primary astrocytes cultured in vitro have shown that process formation involves changes in cytoskeletal proteins and release of tension on the substratum. Actin filament reorganization has previously been found to be the major cytoskeletal change occurring during process formation. These changes are relatively rapid with breakdown of the actin web and release of contacts occur within 15 min. of cyclic AMP treatment. The former is regulated by myosin light chain (MLC) and actin depolymerizing factor (ADF), with MLC involved in the initial release of contractile tension and ADF in both initial and longer term actin breakdown. Our results show that the dephosphorylation of MLC is due to the phosphorylation and inactivation of myosin light chain kinase (MLCK) in response to cyclic AMP. To further study the mechanisms underlying the process formation in astrocytes we used endothelin-1 (ET-1), a vasopeptide which has been shown to inhibit process formation in astrocytes and sodium fluoride which is a general phosphatase inhibitor. We observe an increase in phosphorylation of MLC on inhibition of process formation. To study the role of adhesion in process formation we used suspension cultures of astrocytes. Our results with the astrocytes in suspension suggest that the process formation in astrocytes is adhesion dependent and the changes in ADF and MLC occur only when there is process formation.

摘要

体外培养原代星形胶质细胞的研究表明,突起形成涉及细胞骨架蛋白的变化以及细胞对基质张力的释放。此前已发现肌动蛋白丝重组是突起形成过程中发生的主要细胞骨架变化。这些变化相对较快,在环磷酸腺苷(cAMP)处理15分钟内,肌动蛋白网络就会解体并释放接触。前者受肌球蛋白轻链(MLC)和肌动蛋白解聚因子(ADF)调节,MLC参与收缩张力的初始释放,ADF则参与肌动蛋白的初始和长期分解。我们的结果表明,MLC的去磷酸化是由于肌球蛋白轻链激酶(MLCK)响应cAMP而发生磷酸化并失活。为了进一步研究星形胶质细胞突起形成的潜在机制,我们使用了内皮素-1(ET-1),一种已被证明可抑制星形胶质细胞突起形成的血管肽,以及作为一般磷酸酶抑制剂的氟化钠。我们观察到在抑制突起形成时MLC的磷酸化增加。为了研究黏附在突起形成中的作用,我们使用了星形胶质细胞的悬浮培养。我们对悬浮星形胶质细胞的研究结果表明,星形胶质细胞的突起形成依赖于黏附,并且只有在有突起形成时ADF和MLC才会发生变化。

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