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Interrelationship between activation of matrix metalloproteinases and mitochondrial dysfunction in the development of diabetic retinopathy

机译:糖尿病视网膜病变发展过程中基质金属蛋白酶激活与线粒体功能障碍之间的相互关系

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Mitochondria dysfunction plays a significant role in the apoptosis of retinal cells. Diabetes activates retinal matrix metalloproteinases (MMP-9 and MMP-2), damages retinal mitochondria and activates the apoptotic machinery. This study is to investigate the temporal relationship between the activation of retinal MMPs and mitochondria damage in the development of diabetic retinopathy. Time course of activation of cytosolic MMP-9 and MMP-2 was investigated in the retinal endothelial cells incubated in high glucose for 6-96 h, and correlated with their mitochondrial accumulation and mitochondrial damage. This was confirmed in the retina from rats diabetic for 15 days to similar to 12 months (streptozotocin-induced). The results show that the activation of cytosolic MMP-9 and MMP-2 is an early event, which is followed by their accumulation in the mitochondria. Increased mitochondria! MMPs dysfunction them and begin to damage their DNA, which initiates a vicious cycle of reactive oxygen species. Thus, modulation of these gelatinase MMPs by pharmacological agents during the early stages of diabetes could provide a strategy to inhibit the development of diabetic retinopathy. (C) 2013 Elsevier Inc. All rights reserved.
机译:线粒体功能障碍在视网膜细胞凋亡中起重要作用。糖尿病会激活视网膜基质金属蛋白酶(MMP-9和MMP-2),破坏视网膜线粒体并激活凋亡机制。本研究旨在探讨糖尿病性视网膜病变发展过程中视网膜MMPs激活与线粒体损伤之间的时间关系。研究了在高葡萄糖条件下培养6-96 h的视网膜内皮细胞中胞质MMP-9和MMP-2活化的时程,并与它们的线粒体积累和线粒体损伤相关。在患有糖尿病的大鼠的视网膜中,在15天至12个月的相似时间内证实了这一点(链脲佐菌素诱导的)。结果表明胞质MMP-9和MMP-2的激活是早期事件,其后在线粒体中积累。线粒体增多! MMP使它们功能失调并开始破坏其DNA,从而引发活性氧的恶性循环。因此,在糖尿病的早期阶段,通过药物调节这些明胶酶MMPs可以提供抑制糖尿病性视网膜病发展的策略。 (C)2013 Elsevier Inc.保留所有权利。

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