Active form Notch4 promotes the proliferation and differentiation of 3T3-L1 preadipocytes

被引:22
作者
Lai, Peng-Yeh [1 ,2 ]
Tsai, Chong-Bin [1 ,2 ,3 ]
Tseng, Min-Jen [1 ,2 ]
机构
[1] Natl Chung Cheng Univ, Inst Mol Biol, Chiayi 621, Taiwan
[2] Natl Chung Cheng Univ, Dept Life Sci, Chiayi 621, Taiwan
[3] Chiayi Christian Hosp, Dept Ophthalmol, Chiayi 600, Taiwan
关键词
Notch; 3T3-L1; Adipogenesis; ADIPOCYTE DIFFERENTIATION; C/EBP-ALPHA; PPAR-GAMMA; ADIPOGENESIS; BINDING; TRANSCRIPTION; DEGRADATION; ACTIVATION; EXPRESSION; PROTEIN;
D O I
10.1016/j.bbrc.2012.12.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adipose tissue is composed of adipocytes, which differentiate from precursor cells in a process called adipogenesis. Many signal molecules are involved in the transcriptional control of adipogenesis, including the Notch pathway. Previous adipogenic studies of Notch have focused on Notch1 and HES1; however, the role of other Notch receptors in adipogenesis remains unclear. Q-RT-PCR analyses showed that the augmentation of Notch4 expression during the differentiation of 3T3-L1 preadipocytes was comparable to that of Notch1. To elucidate the role of Notch4 in adipogenesis, the human active form Notch4 (N4IC) was transiently transfected into 3T3-L1 cells. The expression of HES1, Hey1, C/EBP delta and PPAR gamma was up-regulated, and the expression of Pref-1, an adipogenic inhibitor, was down-regulated. To further characterize the effect of N4IC in adipogenesis, stable cells expressing human N4IC were established. The expression of N4IC promoted proliferation and enhanced differentiation of 3T3-L1 cells compared with those of control cells. These data suggest that N4IC promoted proliferation through modulating the ERK pathway and the cell cycle during the early stage of 3T3-L1 adipogenesis and facilitated differentiation through up-regulating adipogenic genes such as C/EBP alpha, PPAR gamma, aP2, LPL and HSL during the middle and late stages of 3T3-L1 adipogenesis. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1132 / 1139
页数:8
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