过剩1
发病机制
葡萄糖转运蛋白
运输机
糖尿病
疾病
医学
葡萄糖摄取
肾脏疾病
生物信息学
内科学
内分泌学
胰岛素
生物
生物化学
基因
作者
Li Zhang,Meiyan Wu,Jizhou Zhang,Tingting Liu,Shaojie Fu,Yue Wang,Zhonggao Xu
出处
期刊:Life Sciences
[Elsevier]
日期:2024-07-26
卷期号:353: 122932-122932
标识
DOI:10.1016/j.lfs.2024.122932
摘要
Diabetes mellitus (DM) is a significant public health problem. Diabetic kidney disease (DKD) is the most common complication of DM, and its incidence has been increasing with the increasing prevalence of DM. Given the association between DKD and mortality in patients with DM, DKD is a significant burden on public health resources. Despite its significance in DM progression, the pathogenesis of DKD remains unclear. Aberrant glucose uptake by cells is an important pathophysiological mechanism underlying DKD renal injury. Glucose is transported across the bilayer cell membrane by a glucose transporter (GLUT) located on the cell membrane. Multiple GLUT proteins have been identified in the kidney, and GLUT1 is one of the most abundantly expressed isoforms. GLUT1 is a crucial regulator of intracellular glucose metabolism and plays a key pathological role in the phenotypic changes in DKD mesangial cells. In an attempt to understand the pathogenesis of DKD better, we here present a review of studies on the role of GLUT1 in the development and progression of DKD.
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