跳轉至內容
Merck
  • Dysfunction of Mitochondrial Dynamics in Drosophila Model of Diabetic Nephropathy.

Dysfunction of Mitochondrial Dynamics in Drosophila Model of Diabetic Nephropathy.

Life (Basel, Switzerland) (2021-01-23)
Kiyoung Kim, Sun Joo Cha, Hyun-Jun Choi, Jeong Suk Kang, Eun Young Lee
摘要

Although mitochondrial dysfunction is associated with the development and progression of diabetic nephropathy (DN), its mechanisms are poorly understood, and it remains debatable whether mitochondrial morphological change is a cause of DN. In this study, a Drosophila DN model was established by treating a chronic high-sucrose diet that exhibits similar phenotypes in animals. Results showed that flies fed a chronic high-sucrose diet exhibited a reduction in lifespan, as well as increased lipid droplets in fat body tissue. Furthermore, the chronic high-sucrose diet effectively induced the morphological abnormalities of nephrocytes in Drosophila. High-sucrose diet induced mitochondria fusion in nephrocytes by increasing Opa1 and Marf expression. These findings establish Drosophila as a useful model for studying novel regulators and molecular mechanisms for imbalanced mitochondrial dynamics in the pathogenesis of DN. Furthermore, understanding the pathology of mitochondrial dysfunction regarding morphological changes in DN would facilitate the development of novel therapeutics.

材料
產品編號
品牌
產品描述

Sigma-Aldrich
山羊抗小鼠IgG抗体,(H + L)HRP共轭标记, 1 mg/mL, Chemicon®
Sigma-Aldrich
山羊抗兔IgG抗体,(H + L)HRP偶联, 1 mg/mL, Chemicon®
Sigma-Aldrich
抗 线粒体融合素-2(N-末端) 兔抗, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
β-甲基巴豆酰基辅酶A 锂盐, ≥90%