自噬
糖尿病
医学
内科学
内分泌学
重症监护医学
生物
生物化学
细胞凋亡
作者
Catherine Arden,S.H. Park,Xaviera Riani Yasasilka,Eun Y. Lee,Myung‐Shik Lee
标识
DOI:10.1016/j.tem.2024.06.010
摘要
Autophagy is critical for energy homeostasis and the function of organelles such as endoplasmic reticulum (ER) and mitochondria. Dysregulated autophagy due to aging, environmental factors, or genetic predisposition can be an underlying cause of not only diabetes through β-cell dysfunction and metabolic inflammation, but also diabetic complications such as diabetic kidney diseases (DKDs). Dysfunction of lysosomes, effector organelles of autophagic degradation, due to metabolic stress or nutrients/metabolites accumulating in metabolic diseases is also emerging as a cause or aggravating element in diabetes and its complications. Here, we discuss the etiological role of dysregulated autophagy and lysosomal dysfunction in diabetes and a potential role of autophagy or lysosomal modulation as a new avenue for treatment of diabetes and its complications.
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