免疫系统
缺氧(环境)
调节器
缺氧诱导因子
主调节器
疾病
1型糖尿病
免疫学
糖酵解
生物
生物信息学
糖尿病
癌症研究
医学
转录因子
内分泌学
新陈代谢
内科学
基因
化学
遗传学
氧气
有机化学
作者
Raphael R. Fagundes,Arnaud Zaldumbide,Cormac T. Taylor
标识
DOI:10.1016/j.tips.2024.07.001
摘要
Type 1 diabetes (T1D) is a common autoimmune disease in which dysregulated glucose metabolism is a key feature. T1D is both poorly understood and in need of improved therapeutics. Hypoxia is frequently encountered in multiple tissues in T1D patients including the pancreas and sites of diabetic complications. Hypoxia-inducible factor (HIF)-1, a ubiquitous master regulator of the adaptive response to hypoxia, promotes glucose metabolism through transcriptional and non-transcriptional mechanisms and alters disease progression in multiple preclinical T1D models. However, how HIF-1 activation in β-cells of the pancreas and immune cells (two key cell types in T1D) ultimately affects disease progression remains controversial. We discuss recent advances in our understanding of the role of hypoxia/HIF-1-induced glycolysis in T1D and explore the possible use of drugs targeting this pathway as potential new therapeutics.
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