高脂饮食对β细胞增殖和β细胞质量的调节

M L Golson, A Ackermann Misfeldt, U G Kopsombut, C P Petersen, M Gannon
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引用次数: 0

摘要

2 型糖尿病(T2D)的特点是胰岛素相对不足,当肝脏、肌肉和脂肪细胞等外周组织对胰岛素的反应减弱时,就会导致胰岛素不足。肥胖是增加胰岛素抵抗和 T2D 风险的一个因素。在未患 T2D 的肥胖患者中,以及在最初患 T2D 的患者中,胰腺 β 细胞能够通过增加增殖和肥大以及增加每个 β 细胞的胰岛素分泌来增加 β 细胞的质量,从而补偿胰岛素抵抗。然而,在发展为 T2D 的患者中,最初的代偿期之后,β 细胞会因增殖减少和凋亡增加而衰竭。叉头盒转录因子 FoxM1 是小鼠四周龄后、妊娠期和胰腺部分切除术后β细胞复制所必需的。我们研究了饮食引起的肥胖是否也需要FoxM1来促进β细胞增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High Fat Diet Regulation of β-Cell Proliferation and β-Cell Mass.

High Fat Diet Regulation of β-Cell Proliferation and β-Cell Mass.

High Fat Diet Regulation of β-Cell Proliferation and β-Cell Mass.

High Fat Diet Regulation of β-Cell Proliferation and β-Cell Mass.

Type 2 Diabetes (T2D) is characterized by relative insulin insufficiency, caused when peripheral tissues such as liver, muscle, and adipocytes have a decreased response to insulin. One factor that elevates the risk for insulin resistance and T2D is obesity. In obese patients without T2D and initially in people who develop T2D, pancreatic β-cells are able to compensate for insulin resistance by increasing β-cell mass, effected by increased proliferation and hypertrophy, as well as increased insulin secretion per β-cell. In patients that go on to develop T2D, however, this initial period of compensation is followed by β-cell failure due to decreased proliferation and increased apoptosis. The forkhead box transcription factor FoxM1 is required for β-cell replication in mice after four weeks of age, during pregnancy, and after partial pancreatectomy. We investigated whether it is also required for β-cell proliferation due to diet-induced obesity.

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