db/db雌性小鼠出生后机体发生过程中肝脏细胞凋亡的研究

S. Michurina, I. Ishchenko, M. A. Cherepanova, S. Arkhipov, Y. Borodin, E. Zavjalov, D. Vasendin
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引用次数: 0

摘要

纯合子小鼠BKS肝细胞中抗凋亡Bcl-2蛋白和促凋亡蛋白Bad表达的免疫组化分析和形态计量学评价对Cg-Dock7m+/+Leprdb/J (db/db小鼠)在产后不同时期(8周龄和16周龄)发生的肥胖和2型糖尿病(DM2)进行研究。在8周龄db/db小鼠的肝脏中,在肝脏毛细血管窦细胞和单个肝细胞的异质群中检测到微弱的Bcl-2和Bcl-2阳性信号。结果发现,DM2对16周龄小鼠两种蛋白的免疫组化染色区域均有所增加。而在成年动物中,Bcl-2的表达面积几乎是Bad的2.5倍。这一事实表明,在db/db小鼠出生后的非酒精性脂肪性肝病(NAFLD)中,肝细胞具有抗凋亡保护作用,并为阻断凋亡线粒体“分支”的发展创造了条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apoptosis in the liver of db/db Mice Female in Postnatal Ontogenesis
Immunohistochemical analysis and morphometric evaluation of the expression of antiapoptotic Bcl-2 protein and proapoptotic protein Bad in the liver cells of homozygous mice BKS.Cg-Dock7m+/+Leprdb/J (db/db mice) females at different periods of postnatal ontogeny (at the age of 8 and 16 weeks) in the development of obesity and diabetes mellitus type 2 (DM2) were done. In the liver of db/db mice at the age of 8 weeks weak Bcl-2 and Bаd-positive signals were detected in the heterogeneous population of sinusoidal cells of the of liver blood capillaries and in single hepatocytes. It was found that immunohistochemical staining areas of both proteins were increased in mice aged 16 weeks with DM2. However in adult animals, Bcl-2 expression area was almost 2,5 times higher than this parameter value for Bad. This fact indicates the antiapoptotic protection of liver cells and the creation of conditions for blocking the development of apoptosis mitochondrial "branch" at non-alcoholic fatty liver disease (NAFLD) in db/db mice postnatal ontogenesis.
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