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ROCK-1 mediates diabetes-induced retinal pigment epithelial and endothelial cell blebbing: Contribution to diabetic retinopathy

机译:ROCK-1介导糖尿病诱导的视网膜色素上皮和内皮细胞起泡:对糖尿病性视网膜病变的贡献

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摘要

In diabetic retinopathy, the exact mechanisms leading to retinal capillary closure and to retinal barriers breakdown remain imperfectly understood. Rho-associated kinase (ROCK), an effector of the small GTPase Rho, involved in cytoskeleton dynamic regulation and cell polarity is activated by hyperglycemia. In one year-old Goto Kakizaki (GK) type 2 diabetic rats retina, ROCK-1 activation was assessed by its cellular distribution and by phosphorylation of its substrates, MYPT1 and MLC. In both GK rat and in human type 2 diabetic retinas, ROCK-1 is activated and associated with non-apoptotic membrane blebbing in retinal vessels and in retinal pigment epithelium (RPE) that respectively form the inner and the outer barriers. Activation of ROCK-1 induces focal vascular constrictions, endoluminal blebbing and subsequent retinal hypoxia. In RPE cells, actin cytoskeleton remodeling and membrane blebs in RPE cells contributes to outer barrier breakdown. Intraocular injection of fasudil, significantly reduces both retinal hypoxia and RPE barrier breakdown. Diabetes-induced cell blebbing may contribute to ischemic maculopathy and represent an intervention target.
机译:在糖尿病性视网膜病中,导致视网膜毛细血管关闭和视网膜屏障破坏的确切机制仍未得到很好的理解。 Rho相关激酶(ROCK)是小GTPase Rho的效应子,参与细胞骨架动态调节和细胞极性被高血糖激活。在1岁的Goto Kakizaki(GK)2型糖尿病大鼠视网膜中,ROCK-1的激活通过细胞分布以及底物MYPT1和MLC的磷酸化来评估。在GK大鼠和人类2型糖尿病视网膜中,ROCK-1均被激活并与视网膜血管和视网膜色素上皮(RPE)中的非凋亡膜起泡相关,后者分别形成内部和外部屏障。 ROCK-1的激活引起局灶性血管收缩,腔内起泡以及随后的视网膜缺氧。在RPE细胞中,RPE细胞中的肌动蛋白细胞骨架重塑和膜起泡有助于外壁屏障的破坏。眼内注射法舒地尔可显着减少视网膜缺氧和RPE屏障破坏。糖尿病引起的细胞起泡可能会导致缺血性黄斑病变,并成为干预目标。

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