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Lipid domain-dependent regulation of single-cell wound repair

机译:脂质域依赖的单细胞伤口修复调控

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摘要

After damage, cells reseal their plasma membrane and repair the underlying cortical cytoskeleton. Although many different proteins have been implicated in cell repair, the potential role of specific lipids has not been explored. Here we report that cell damage elicits rapid formation of spatially organized lipid domains around the damage site, with different lipids concentrated in different domains as a result of both de novo synthesis and transport. One of these lipids-diacylglycerol (DAG)-rapidly accumulates in a broad domain that overlaps the zones of active Rho and Cdc42, GTPases that regulate repair of the cortical cytoskeleton. Formation of the DAG domain is required for Cdc42 and Rho activation and healing. Two DAG targets, protein kinase C (PKC) β and η, are recruited to cell wounds and play mutually antagonistic roles in the healing process:PKCβ participates in Rho and Cdc42 activation, whereas PKCη inhibits Rho and Cdc42 activation. The results reveal an unexpected diversity in subcellular lipid domains and the importance of such domains for a basic cellular process.
机译:受损后,细胞会重新密封其质膜并修复潜在的皮质细胞骨架。尽管许多不同的蛋白质与细胞修复有关,但尚未探索特定脂质的潜在作用。在这里我们报告细胞损伤引起损伤部位周围空间组织脂质域的快速形成,由于从头合成和运输的结果是不同的脂质集中在不同的域中。这些脂质-二甘油甘油(DAG)中的一种迅速积聚在一个宽域中,该区域与活性Rho和Cdc42,调节皮质细胞骨架修复的GTpases区域重叠。 Ddc结构域的形成是Cdc42和Rho激活和愈合所必需的。将两个DAG靶蛋白激酶C(PKC)β和η募集到细胞伤口上,并在愈合过程中起相互拮抗的作用:PKCβ参与Rho和Cdc42的激活,而PKCη抑制Rho和Cdc42的激活。结果揭示了亚细胞脂质结构域中意想不到的多样性,以及这些结构域对于基本细胞过程的重要性。

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