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磷脂酶Cγ负向调节抗原刺激的肥大细胞中Rac/Cdc42的激活。

Phospholipase C gamma negatively regulates Rac/Cdc42 activation in antigen-stimulated mast cells.

作者信息

El-Sibai Mirvat, Backer Jonathan M

机构信息

Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Eur J Immunol. 2007 Jan;37(1):261-70. doi: 10.1002/eji.200635875.

Abstract

The Rho GTPases Rac and Cdc42 play a central role in the regulation of secretory and cytoskeletal responses in antigen-stimulated mast cells. In this study, we examine the kinetics and mechanism of Rac and Cdc42 activation in the rat basophilic leukemia RBL-2H3 cells. The activation kinetics of both Rac and Cdc42 show a biphasic profile, consisting of an early transient peak at 1 min and a late sustained activation phase at 20-40 min. The inhibition of phospholipase C (PLC)gamma causes a twofold increase in Rac and Cdc42 activation that coincides with a dramatic production of atypical filopodia-like structures. Inhibition of protein kinase C using bisindolylmaleimide mimics the effect of PLCgamma inhibition on Rac activation, but not on Cdc42 activation. In contrast, depletion of intracellular calcium leads to a complete inhibition of the early activation peak of both Rac and Cdc42, without significant effects on the late sustained activation. These data suggest that PLCgamma is involved in a negative feedback loop that leads to the inhibition of Rac and Cdc42. They also suggest that the presence of intracellular calcium is a prerequisite for both Rac and Cdc42 activation.

摘要

Rho GTPases蛋白Rac和Cdc42在抗原刺激的肥大细胞分泌和细胞骨架反应的调节中起核心作用。在本研究中,我们检测了大鼠嗜碱性白血病RBL - 2H3细胞中Rac和Cdc42激活的动力学和机制。Rac和Cdc42的激活动力学均呈现双相特征,包括1分钟时的早期瞬时峰值和20 - 40分钟时的晚期持续激活阶段。磷脂酶C(PLC)γ的抑制导致Rac和Cdc42激活增加两倍,这与非典型丝状伪足样结构的大量产生相吻合。使用双吲哚马来酰亚胺抑制蛋白激酶C模拟了PLCγ抑制对Rac激活的作用,但对Cdc42激活无此作用。相反,细胞内钙的耗竭导致Rac和Cdc42早期激活峰值完全被抑制,而对晚期持续激活无显著影响。这些数据表明PLCγ参与了导致Rac和Cdc42抑制的负反馈回路。它们还表明细胞内钙的存在是Rac和Cdc42激活的先决条件。

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