内质网
发病机制
自噬
线粒体
细胞器
医学
线粒体融合
疾病
细胞生物学
生物信息学
生物
病理
生物化学
细胞凋亡
线粒体DNA
基因
作者
Yong Liu,Yingjin Qiao,Shaokang Pan,Jingfang Chen,Zi‐Hui Mao,Kaidi Ren,Yang Yang,Qi Feng,Dongwei Liu,Zhangsuo Liu
摘要
Diabetic kidney disease (DKD) is a global health issue that presents a complex pathogenesis and limited treatment options.To provide guidance for precise therapies, it is crucial to accurately identify the pathogenesis of DKD.Several studies have recognized that mitochondrial and endoplasmic reticulum (ER) dysfunction are key drivers of the pathogenesis of DKD.The mitochondria-associated ER membrane (MAM) is a dynamic membrane contact site (MSC) that connects the ER and mitochondria and is essential in maintaining the normal function of the two organelles.MAM is involved in various cellular processes, including lipid synthesis and transport, calcium homeostasis, mitochondrial fusion and fission, and ER stress.Meanwhile, recent studies confirm that MAM plays a significant role in the pathogenesis of DKD by regulating glucose metabolism, lipid metabolism, inflammation, ER stress, mitochondrial fission and fusion, and autophagy.Herein, this review aims to provide a comprehensive summary of the physiological function of MAMs and their impact on the progression of DKD.Subsequently, we discuss the trend of pharmaceutical studies that target MAM resident proteins for treating DKD.Furthermore, we also explore the future development prospects of MAM in DKD research, thereby providing a new perspective for basic studies and clinical treatment of DKD.
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