Willmes Diana M, Birkenfeld Andreas L
Department of Endocrinology, Diabetes and Nutrition, Center for Cardiovascular Research, Charité - University School of Medicine, Berlin, Germany.
Comput Struct Biotechnol J. 2013 Dec 8;6:e201303020. doi: 10.5936/csbj.201303020. eCollection 2013.
Reduced expression of the Indy (I'm Not Dead Yet) gene in D. melanogaster and C. elegans extends longevity. Indy and its mammalian homolog mINDY (Slc 3a5, NaCT) are transporters of TCA cycle intermediates, mainly handling the uptake of citrate via the plasma membrane into the cytosol. Deletion of mINDY in mice leads to significant metabolic changes akin to caloric restriction, likely caused by reducing the effects of mINDY-imported citrate on fatty acid and cholesterol synthesis, glucose metabolism and ß-oxidation. This review will provide an overview on different mammalian SLC 3 family members with a focus on mINDY (SLC 3A5) in glucose and energy metabolism and will highlight the role of mINDY as a putative therapeutic target for the treatment of obesity, non-alcoholic fatty liver disease and type 2 diabetes.
Indy(我还没死)基因在黑腹果蝇和秀丽隐杆线虫中的表达降低可延长寿命。Indy及其哺乳动物同源物mINDY(Slc 3a5,NaCT)是三羧酸循环中间产物的转运体,主要负责将柠檬酸通过质膜摄取到细胞质中。小鼠中mINDY的缺失会导致类似于热量限制的显著代谢变化,这可能是由于减少了mINDY导入的柠檬酸对脂肪酸和胆固醇合成、葡萄糖代谢及β-氧化的影响所致。本综述将概述不同的哺乳动物SLC 3家族成员,重点关注mINDY(SLC 3A5)在葡萄糖和能量代谢中的作用,并强调mINDY作为肥胖症、非酒精性脂肪性肝病和2型糖尿病治疗的潜在治疗靶点的作用。