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血小板活化因子刺激脑微血管中的蛋白激酶C易位。

Platelet-activating factor stimulates protein kinase C translocation in cerebral microvessels.

作者信息

Catalán R E, Martínez A M, Aragonés M D, Garde E, Díaz G

机构信息

Departamento de Biología Molecular, Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Spain.

出版信息

Biochem Biophys Res Commun. 1993 Apr 30;192(2):446-51. doi: 10.1006/bbrc.1993.1435.

Abstract

The effects of platelet-activating factor (PAF) on distribution of protein kinase C activity in brain microvessels have been examined. Our results indicate that PAF caused an increase of protein kinase C activity in membrane, accompanied by a loss of activity in the cytosol. This effect resulted to be dose-dependent and the translocation was evident after 30 min of PAF treatment. These results suggest that PAF could play a role in transport processes in the blood-brain barrier, involving protein phosphorylation by activation of protein kinase C.

摘要

研究了血小板活化因子(PAF)对脑微血管中蛋白激酶C活性分布的影响。我们的结果表明,PAF导致膜中蛋白激酶C活性增加,同时伴随着胞质溶胶中活性丧失。这种效应呈剂量依赖性,PAF处理30分钟后易位明显。这些结果表明,PAF可能在血脑屏障的转运过程中发挥作用,涉及通过激活蛋白激酶C进行蛋白磷酸化。

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