Autophagy: Emerging Therapeutic Target for Diabetic Nephropathy

被引:53
|
作者
Kume, Shinji [1 ]
Yamahara, Kosuke [1 ]
Yasuda, Mako [1 ]
Maegawa, Hiroshi [1 ]
Koya, Daisuke [2 ]
机构
[1] Shiga Univ Med Sci, Dept Med, Otsu, Shiga 52021, Japan
[2] Kanazawa Med Univ, Uchinada, Ishikawa 9200293, Japan
关键词
Autophagy; diabetic nephropathy; mTORC1; AMPK; proteinuria; ATTENUATES RENAL HYPERTROPHY; BETA-CELL MASS; INSULIN-RESISTANCE; PODOCYTE FUNCTION; CISPLATIN INJURY; PROTEIN-KINASE; GROWTH-CONTROL; MTOR PATHWAY; PROGRESSION; INHIBITION;
D O I
10.1016/j.semnephrol.2013.11.003
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Autophagy is a major catabolic pathway by which mammalian cells degrade and recycle macromolecules and organelles. It plays a critical role in removing protein aggregates, as well as damaged or excess organelles, to maintain intracellular homeostasis and to keep cells healthy. The accumulation of damaged proteins and organelles induced by hyperglycemia and other metabolic alterations is strongly associated with the development of diabetic nephropathy. Autophagy is up-regulated under conditions of calorie restriction and environmental stress, such as oxidative stress and hypoxia in proximal tubular cells, and occurs even under normal conditions in podocytes. These findings have led to our hypothesis that autophagy is involved in the pathogenesis of diabetic nephropathy, a hypothesis increasingly supported by experimental evidence. To date, however, the exact role of autophagy in diabetic nephropathy has not been fully revealed. This article therefore reviews recent findings and provides perspectives on the involvement of autophagy in diabetic nephropathy. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
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