HDAC6型
胰岛素
内分泌学
胰岛
内科学
胰腺
信号转导
HDAC10型
糖尿病
胰岛素受体
细胞生物学
生物
组蛋白
癌症研究
组蛋白脱乙酰基酶
化学
医学
小岛
胰岛素抵抗
生物化学
基因
作者
Hiroyuki Inoue,Shun‐ichiro Asahara,Yumiko Sugiura,Yukina Kawada,Asuka Imai,Chisako Hara,Ayumi Kanno,Maki Kimura-Koyanagi,Yoshiaki Kido
标识
DOI:10.1016/j.bbrc.2020.10.078
摘要
The reduction of pancreatic β cell mass is one of the key factors for the onset of type 2 diabetes. Many reports have indicated that insulin signaling is important for type 2 diabetes, but the mechanism by which insulin signaling is altered in pancreatic β cells remains unclear. This study was designed to examine the role of histone deacetylases (HDACs) in the regulation of insulin signaling in pancreatic β cells. We found that insulin signaling was downregulated by inhibition of HDAC6. HDAC6 expression was specifically observed in pancreatic β cells and was decreased in the pancreatic islets of a type 2 diabetes mouse model. When a mouse pancreatic β cell line (MIN6 cells) was treated with palmitic acid to mimic the effect of a high-fat diet on pancreatic β cells, HDAC6 was imported into the nucleus. These results suggest that HDAC6 plays an important role in the regulation of insulin signaling in pancreatic β cells. Therefore, clarifying the regulation of insulin signaling by HDAC6 may be a valuable approach for the treatment of type 2 diabetes.
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