CCAAT/enhancer binding protein α maintains the ability of insulin-stimulated GLUT4 translocation in 3T3-C2 fibroblastic cells

被引:3
作者
Fujimoto, M
Masuzaki, H
Yamamoto, Y
Norisada, N
Imori, M
Yoshimoto, M
Tomita, T
Tanaka, T
Okazawa, K
Fujikura, J
Chusho, H
Ebihara, K
Hayashi, T
Hosoda, K
Inoue, G
Nakao, K
机构
[1] Kyoto Univ, Dept Med & Clin Sci, Div Endocrinol & Metab, Grad Sch Med,Sakyo Ku, Kyoto 6068507, Japan
[2] Fujisawa Pharmaceut Co Ltd, Inst Res & Dev, Osaka 532, Japan
[3] Kyoto Univ, Grad Sch Human & Environm Studies, Kyoto, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2005年 / 1745卷 / 01期
关键词
GLUT4; translocation; 3T3-C2; fibroblast; C/EBP alpha; peroxisome proliferator-activated receptor gamma; adipogenesis;
D O I
10.1016/j.bbamcr.2004.12.007
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
In 3T3-L1 preadipocytes, hormonal induction causes adipose conversion and facilitates the expression of insulin-sensitive glucose transporter, GLUT4. Evidence has accumulated that, in 3T3-L1 preadipocytes, the formation of GLUT4 storage vesicle and its translocation to plasma membrane precede both lipid accumulation and expression of GLUT4 and C/EBP alpha a key transcription factor for adipose differentiation. On the other hand, 3T3-C2 fibroblastic cells, a subline of 3T3-L1, follow adipogenic process till mitotic clonal expansion stage (2 days after hormonal induction), but do not proceed to terminal differentiation stage (8 days after the induction), resulting in a lack of adipose conversion and GLUT4 expression. Here we show that, when myc-tagged GLUT4 was retrovirally expressed in 3T3-C2 cells, insulin-stimulated GLUT4 translocation did occur on day 2 after the induction. On day 8 after the induction, however, neither GLUT4 translocation nor the expression of C/EBPa was observed. We also created 3T3-C2 cells stably expressing both myc-tagged GLUT4 and C/EBT alpha demonstrating that co-expressed cells showed insulin-stimulated GLUT4 translocation on day 8 after the induction, as well as adipose conversion coupling with PPAR gamma expression. Our results provide evidence that C/EBPa has the potential to maintain the ability of insulin-stimulated GLUT4 translocation in C/EBP alpha-deficient 3T3-C2 fibroblastic cells. (c) 2004 Elsevier B.V All rights reserved.
引用
收藏
页码:38 / 47
页数:10
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