Identification of novel putative membrane proteins selectively expressed during adipose conversion of 3T3-L1 cells

被引:42
作者
Xu, AM
Choi, KL
Wang, Y
Parmana, PA
Xu, LY
Bogardus, C
Cooper, GJS
机构
[1] Univ Auckland, Sch Biol Sci, Auckland 1, New Zealand
[2] NIDDKD, Phoenix Epidemiol & Clin Res Branch, NIH, Phoenix, AZ 85016 USA
关键词
adipogenesis; proteomics; insulin; metabolism; membrane protein;
D O I
10.1016/S0006-291X(02)00354-6
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
Fat tissue plays a critical role in the regulation of energy metabolism. Here we report the proteomic identification of a novel fat tissue-specific low molecular weight protein (Falp) which responds to insulin. Falp is preferentially expressed in adipocytes but not in preadipocytes, as shown by two-dimensional gel electrophoresis. Northern blot analysis shows that the Falp gene is predominantly expressed in brown and white fat tissues, but not in any other tissues examined. Human homologs of mouse Falp are found to exist as two alternatively spliced isoforms, which share the same N-terminus but have different C-termini. Both human and mouse Falp contain a conserved putative transmembrane domain. Immunofluorescent analyses of 3T3-L1 adipocytes show that Falp protein strictly localizes at a compact perinuclear membrane compartment. Treatment of cells with insulin induces the redistribution of Falp into numerous discrete spotty structures spreading throughout the cytoplasm. Whereas the function of Falp is currently unclear, its tissue specific expression and the responsiveness to insulin suggest that Falp might be involved in a process specifically restricted to adipose tissue function, such as vesicular transport and protein secretion. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1161 / 1167
页数:7
相关论文
共 32 条
[1]   Insulin stimulates both leptin secretion and production by rat white adipose tissue [J].
Barr, VA ;
Malide, D ;
Zarnowski, MJ ;
Taylor, SI ;
Cushman, SW .
ENDOCRINOLOGY, 1997, 138 (10) :4463-4472
[2]   Adiponutrin, a transmembrane protein corresponding to a novel dietary- and obesity-linked mRNA specifically expressed in the adipose lineage [J].
Baulande, S ;
Lasnier, F ;
Lucas, M ;
Pairault, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) :33336-33344
[3]   Central role of the adipocyte in the metabolic syndrome [J].
Bergman, RN ;
Van Citters, GW ;
Mittelman, SD ;
Dea, MK ;
Hamilton-Wessler, M ;
Kim, SP ;
Ellmerer, M .
JOURNAL OF INVESTIGATIVE MEDICINE, 2001, 49 (01) :119-126
[4]   Two compartments for insulin-stimulated exocytosis in 3T3-L1 adipocytes defined by endogenous ACRP30 and GLUT4 [J].
Bogan, JS ;
Lodish, HF .
JOURNAL OF CELL BIOLOGY, 1999, 146 (03) :609-620
[5]   The adipocyte as a secretory organ: Mechanisms of vesicle transport and secretory pathways [J].
Bradley, RL ;
Cleveland, KA ;
Cheatham, B .
RECENT PROGRESS IN HORMONE RESEARCH, VOL 56, 2001, 56 :329-358
[6]   REGULATION OF ADIPOCYTE DEVELOPMENT [J].
CORNELIUS, P ;
MACDOUGALD, OA ;
LANE, MD .
ANNUAL REVIEW OF NUTRITION, 1994, 14 :99-129
[7]   The adipocyte:: a model for integration of endocrine and metabolic signaling in energy metabolism regulation [J].
Frühbeck, G ;
Gómez-Ambrosi, J ;
Muruzábal, FJ ;
Burrell, MA .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (06) :E827-E847
[8]   Insulin resistance in human partial lipodystrophy. [J].
Hegele R.A. .
Current Atherosclerosis Reports, 2000, 2 (5) :397-404
[9]  
HOFMANN K, 1993, BIOL CHEM HOPPESEYLE, V347, P166
[10]   Moving the insulin-regulated glucose transporter GLUT4 into and out of storage [J].
Holman, GD ;
Sandoval, IV .
TRENDS IN CELL BIOLOGY, 2001, 11 (04) :173-179