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原代培养足细胞的活力与细胞外高糖依赖性自噬下调有关。

Viability of primary cultured podocytes is associated with extracellular high glucose-dependent autophagy downregulation.

作者信息

Audzeyenka Irena, Rogacka Dorota, Piwkowska Agnieszka, Angielski Stefan, Jankowski Maciej

机构信息

Department of Molecular and Cellular Nephrology, Mossakowski Medical Research Centre, Polish Academy of Sciences, Dębinki 7, 80-211, Gdansk, Poland.

Department of Clinical Chemistry, Medical University of Gdansk, Gdansk, Poland.

出版信息

Mol Cell Biochem. 2017 Jun;430(1-2):11-19. doi: 10.1007/s11010-017-2949-5. Epub 2017 Feb 24.

Abstract

Structural and functional impairment of podocytes plays an important role in the development of diabetic nephropathy, a chronic complication of diabetes mellitus and leading cause of renal failure requiring renal replacement therapy. Autophagy plays a crucial role in podocyte viability and function, and its activity is modulated by a variety of pathophysiological factors found in diabetic milieu. Here we show that downregulation of autophagy is critical for podocyte survival in hyperglycemic environment. Moreover, long-term exposure to high glucose leads to inhibition of autophagy as well as to the development of insulin resistance in podocytes. Furthermore, impairment of autophagy is involved in alteration of insulin-dependent glucose uptake in podocytes, suggesting a relationship between these two processes. Taken together, our findings suggest that downregulation of podocyte autophagy, observed after long-term exposure to high glucose, results from their suppressed sensitivity to insulin, and may therefore lead to diminished podocyte cell viability as well as their reduced number in glomerulus.

摘要

足细胞的结构和功能损伤在糖尿病肾病的发展中起重要作用,糖尿病肾病是糖尿病的一种慢性并发症,也是需要肾脏替代治疗的肾衰竭的主要原因。自噬在足细胞的存活和功能中起关键作用,其活性受糖尿病环境中多种病理生理因素的调节。在此我们表明,自噬的下调对高血糖环境中足细胞的存活至关重要。此外,长期暴露于高糖会导致足细胞自噬受到抑制以及胰岛素抵抗的发生。此外,自噬受损参与了足细胞中胰岛素依赖性葡萄糖摄取的改变,提示这两个过程之间存在关联。综上所述,我们的研究结果表明,长期暴露于高糖后观察到的足细胞自噬下调是由于其对胰岛素的敏感性受到抑制,因此可能导致足细胞活力降低以及肾小球中足细胞数量减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64ed/5437172/c23d919bebfe/11010_2017_2949_Fig1_HTML.jpg

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