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鸡卵清蛋白上游启动子转录因子II(COUP-TFII)调节出生后小鼠小脑的生长和模式形成。

Chicken Ovalbumin Upstream Promoter-Transcription Factor II (COUP-TFII) regulates growth and patterning of the postnatal mouse cerebellum.

作者信息

Kim Bum Jun, Takamoto Norio, Yan Jun, Tsai Sophia Y, Tsai Ming-Jer

机构信息

Department of Molecular and Cellular Biology and Development Program, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Dev Biol. 2009 Feb 15;326(2):378-91. doi: 10.1016/j.ydbio.2008.11.001. Epub 2008 Nov 14.

Abstract

COUP-TFII (also known as Nr2f2), a member of the nuclear orphan receptor superfamily, is expressed in several regions of the central nervous system (CNS), including the ventral thalamus, hypothalamus, midbrain, pons, and spinal cord. To address the function of COUP-TFII in the CNS, we generated conditional COUP-TFII knockout mice using a tissue-specific NSE-Cre recombinase. Ablation of COUP-TFII in the brain resulted in malformation of the lobule VI in the cerebellum and a decrease in differentiation of cerebellar neurons and cerebellar growth. The decrease in cerebellar growth in NSE(Cre/+)/CII(F/F) mice is due to reduced proliferation and increased apoptosis in granule cell precursors (GCPs). Additional studies demonstrated that insulin like growth factor 1 (IGF-1) expression was reduced in the cerebellum of NSE(Cre/+)/CII(F/F) mice, thereby leading to decreased Akt1 and GSK-3beta activities, and the reduced expression of mTOR. Using ChIP assays, we demonstrated that COUP-TFII was recruited to the promoter region of IGF-1 in a Sp1-dependent manner. In addition, dendritic branching of Purkinje cells was decreased in the mutant mice. Thus, our results indicate that COUP-TFII regulates growth and maturation of the mouse postnatal cerebellum through modulation of IGF-1 expression.

摘要

COUP - TFII(也称为Nr2f2)是核孤儿受体超家族的成员,在中枢神经系统(CNS)的几个区域表达,包括腹侧丘脑、下丘脑、中脑、脑桥和脊髓。为了研究COUP - TFII在中枢神经系统中的功能,我们使用组织特异性的NSE - Cre重组酶生成了条件性COUP - TFII基因敲除小鼠。大脑中COUP - TFII的缺失导致小脑小叶VI畸形,以及小脑神经元分化和小脑生长减少。NSE(Cre/+)/CII(F/F)小鼠小脑生长减少是由于颗粒细胞前体(GCPs)增殖减少和凋亡增加所致。进一步的研究表明,NSE(Cre/+)/CII(F/F)小鼠小脑中胰岛素样生长因子1(IGF - 1)的表达降低,从而导致Akt1和GSK - 3β活性降低,以及mTOR表达减少。使用染色质免疫沉淀(ChIP)分析,我们证明COUP - TFII以Sp1依赖的方式被招募到IGF - 1的启动子区域。此外,突变小鼠浦肯野细胞的树突分支减少。因此,我们的结果表明,COUP - TFII通过调节IGF - 1的表达来调节小鼠出生后小脑的生长和成熟。

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