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胰岛素耗竭导致肥胖小鼠而非瘦小鼠出现脂肪特异性细胞死亡。

Insulin depletion leads to adipose-specific cell death in obese but not lean mice.

作者信息

Loftus T M, Kuhajda F P, Lane M D

机构信息

Department of Biological Chemistry, Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14168-72. doi: 10.1073/pnas.95.24.14168.

Abstract

Mutation of the obese gene produces obesity, hyperinsulinemia, and compensatory "overexpression" of the defective gene. As insulin activates obese gene expression, it seemed possible that hyperinsulinemia might be responsible for overexpression of the gene. To address this question we rapidly neutralized circulating insulin by injection of an insulin antibody. Unexpectedly, insulin depletion in obese (ob/ob or db/db) mice caused massive adipose RNA degradation confirmed by histological analysis to result from adipocyte cell death by a largely necrotic mechanism. This effect was not observed in lean littermates and was completely corrected by coadministration of insulin. Comparison of multiple tissues demonstrated that the effect was restricted to adipose tissue. Insulin depletion in obese mice by administration of streptozotocin also led to cell death, but this death was less extensive and appeared to be apoptotic in mechanism. Thus insulin may promote the survival side of the physiological balance between adipocyte survival and death.

摘要

肥胖基因的突变会导致肥胖、高胰岛素血症以及缺陷基因的代偿性“过度表达”。由于胰岛素会激活肥胖基因的表达,因此高胰岛素血症可能是该基因过度表达的原因。为了解决这个问题,我们通过注射胰岛素抗体迅速中和循环胰岛素。出乎意料的是,肥胖(ob/ob或db/db)小鼠体内胰岛素耗竭导致大量脂肪RNA降解,组织学分析证实这是由脂肪细胞通过主要为坏死机制的细胞死亡所致。在瘦的同窝小鼠中未观察到这种效应,同时给予胰岛素可完全纠正该效应。对多种组织的比较表明,这种效应仅限于脂肪组织。通过给予链脲佐菌素使肥胖小鼠体内胰岛素耗竭也会导致细胞死亡,但这种死亡范围较小,且机制上似乎是凋亡性的。因此,胰岛素可能促进脂肪细胞存活与死亡之间生理平衡中存活这一方面。

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