Functional characterization of human mesenchymal stem cell-derived adipocytes

被引:100
作者
Rydén, M [1 ]
Dicker, A
Götherström, C
Åström, G
Tammik, C
Arner, P
Le Blanc, K
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Ctr Metab & Endocrinol, Dept Med, S-14186 Stockholm, Sweden
[2] Huddinge Univ Hosp, Karolinska Inst, Div Immunol, Dept Lab Med, S-14186 Stockholm, Sweden
关键词
stem cell; differentiation; adipocyte; lipolysis; antilipolysis; alpha 2A adrenoceptor; HSL; PDE;
D O I
10.1016/j.bbrc.2003.10.010
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
The function of adipocytes derived from human mesenchymal stem cells (hMSC) was investigated for the first time in hMSC from fetal liver (FL) and adult bone marrow (BM) and compared with preadipocytes from human subcutaneous adipose tissue differentiated according to adipocyte-specific protocols. FL- and BM-derived adipocytes displayed both morphological and functional characteristics of mature adipocytes including specific intracellular signaling pathways for tumor necrosis factor-alpha, catecholamine-regulated lipolysis as well as secretion of adiponectin and leptin. Similar to differentiated preadipocytes, hMSC adipocytes displayed lipolytic effects mediated by beta-adrenoceptors and antilipolytic effects mediated by the alpha2A-adrenoceptor (alpha2A-AR) and expressed proteins with a pivotal role in human lipolysis, including beta2-AR, alpha2A-AR, and hormone-sensitive lipase. We conclude that hMSC-derived adipocytes are morphologically and functionally similar to preadipocytes and display an intact lipolytic signaling pathway and endocrine function. These systems could be of great value in adipocyte research as a renewable source of adipocytes. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:391 / 397
页数:7
相关论文
共 20 条
  • [1] Human adipocytes express alpha(2)-adrenergic receptor of the alpha(2)-subtype only: Pharmacological and genetic evidence
    Castan, I
    Devedjian, JC
    Valet, P
    Paris, H
    Lafontan, M
    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1995, 9 (06) : 569 - 575
  • [2] CASTAN L, 1994, AM J PHYSIOL, V266, pR1141
  • [3] Phosphorylation and activation of hormone-sensitive adipocyte phosphodiesterase type 3B
    Degerman, E
    Landstrom, TR
    Wijkander, J
    Holst, LS
    Ahmad, F
    Belfrage, P
    Manganiello, V
    [J]. METHODS, 1998, 14 (01) : 43 - 53
  • [4] DEMONSTRATION OF AN IN-VIVO FUNCTIONAL BETA(3)-ADRENOCEPTOR IN MAN
    ENOCKSSON, S
    SHIMIZU, M
    LONNQVIST, F
    NORDENSTROM, J
    ARNER, P
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) : 2239 - 2245
  • [5] Mechanisms behind lipolytic catecholamine resistance of subcutaneous fat cells in the polycystic ovarian syndrome
    Faulds, G
    Rydén, M
    Ek, I
    Wahrenberg, H
    Arner, P
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (05) : 2269 - 2273
  • [6] Integrative physiology of human adipose tissue
    Frayn, KN
    Karpe, F
    Fielding, BA
    Macdonald, IA
    Coppack, SW
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2003, 27 (08) : 875 - 888
  • [7] Immunomodulatory effects of human foetal liver-derived mesenchymal stem cells
    Götherström, C
    Ringdén, O
    Westgren, M
    Tammik, C
    Le Blanc, K
    [J]. BONE MARROW TRANSPLANTATION, 2003, 32 (03) : 265 - 272
  • [8] PROMOTING EFFECT OF GLUCOCORTICOIDS ON THE DIFFERENTIATION OF HUMAN ADIPOCYTE PRECURSOR CELLS CULTURED IN A CHEMICALLY DEFINED MEDIUM
    HAUNER, H
    ENTENMANN, G
    WABITSCH, M
    GAILLARD, D
    AILHAUD, G
    NEGREL, R
    PFEIFFER, EF
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) : 1663 - 1670
  • [9] MECHANISMS FOR DIFFERENCES IN LIPOLYSIS BETWEEN HUMAN SUBCUTANEOUS AND OMENTAL FAT-CELLS
    HELLMER, J
    MARCUS, C
    SONNENFELD, T
    ARNER, P
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 75 (01) : 15 - 20
  • [10] AdipoQ is a novel adipose-specific gene dysregulated in obesity
    Hu, E
    Liang, P
    Spiegelman, BM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) : 10697 - 10703