Comparison of proliferation and differentiation capacity of human adipocyte precursor cells from the omental and subcutaneous adipose tissue depot of obese subjects

被引:203
作者
van Harmelen, V [1 ]
Röhrig, K [1 ]
Hauner, H [1 ]
机构
[1] Tech Univ Munich, Else Kroner Fresenius Zentrum Ernahrungsmed, D-85350 Freising Weihenstephan, Germany
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2004年 / 53卷 / 05期
关键词
D O I
10.1016/j.metabol.2003.11.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Upper body obesity is characterized by an expansion of the visceral adipose tissue and is associated with an increased susceptibility for type 2 diabetes and cardiovascular disease. In order to get a better understanding of the regulation of body fat distribution, the aim of the present study was to compare adipocyte development between the omental and subcutaneous adipose tissue region in obese subjects. Therefore, the proliferation and differentiation capacity in primary cultures of adipose tissue-derived stromal cells were compared between the 2 depots in a group of 29 obese individuals, of which 21 were women. Proliferation of the cells was stimulated using fetal calf serum (FCS) and assessed by counting the cell number in the culture dishes. Differentiation of preadipocytes was assessed in parallel by morphological criteria and determination of glycerol-3-phosphate dehydrogenase (GPDH) after stimulation by standardized adipogenic conditions. Stromal cells from the subcutaneous adipose tissue region proliferated faster (doubling time, 4 1 days) than those from the omental region (doubling time, 5 1 days), whereas there was no regional difference in adipose differentiation with any of the adipogenic media. The same findings were observed when men were excluded from the analysis. Interestingly, there were more endothelial cells in the cultures from the omental tissue as compared to those from the subcutaneous tissue, but there was no correlation between endothelial cell contamination and proliferation capacity, suggesting that the regional difference in proliferation capacity was not due to regional differences in the amount of endothelial cells. In addition, we found a negative correlation between donor age and proliferation of subcutaneous cells but not of omental cells, possibly explaining the greater capacity for adipose tissue growth in the omental as compared to the subcutaneous depot with aging. In conclusion, there may exist regional differences in adipose tissue growth with regard to proliferation capacity, whereas there are apparently no significant differences in in vitro differentiation capacity between subcutaneous and omental preadipocytes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:632 / 637
页数:6
相关论文
共 23 条
[1]  
Ailhaud G., 1998, HDB OBESITY, P359
[2]  
Arner P, 2001, BIOCHEM SOC T, V29, P72, DOI 10.1042/bst0290072
[3]   DIFFERENCES IN LIPOLYSIS BETWEEN HUMAN SUBCUTANEOUS AND OMENTAL ADIPOSE TISSUES [J].
ARNER, P .
ANNALS OF MEDICINE, 1995, 27 (04) :435-438
[4]   ADIPOSE-TISSUE THYMIDINE KINASE-ACTIVITY IN MAN [J].
BAUM, D ;
BECK, RQ ;
HAMMER, LD ;
BRASEL, JA ;
GREENWOOD, MRC .
PEDIATRIC RESEARCH, 1986, 20 (02) :118-121
[5]  
BJORNTORP P, 1988, DIABETES METAB REV, V4, P615, DOI 10.1002/dmr.5610040607
[6]   Immnohistochemical and ultrastructural localization of leptin and leptin receptor in human white adipose tissue and differentiating human adipose cells in primary culture [J].
Bornstein, SR ;
Abu-Asab, M ;
Glasow, A ;
Päth, G ;
Hauner, H ;
Tsokos, M ;
Chrousos, GP ;
Scherbaum, WA .
DIABETES, 2000, 49 (04) :532-538
[7]  
HAUNER H, 1991, INT J OBESITY, V15, P121
[8]  
Hauner H, 1988, Horm Metab Res Suppl, V19, P35
[9]   PROMOTING EFFECT OF GLUCOCORTICOIDS ON THE DIFFERENTIATION OF HUMAN ADIPOCYTE PRECURSOR CELLS CULTURED IN A CHEMICALLY DEFINED MEDIUM [J].
HAUNER, H ;
ENTENMANN, G ;
WABITSCH, M ;
GAILLARD, D ;
AILHAUD, G ;
NEGREL, R ;
PFEIFFER, EF .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) :1663-1670
[10]   ENDOTHELIN-1 INHIBITS THE ADIPOSE DIFFERENTIATION OF CULTURED HUMAN ADIPOCYTE PRECURSOR CELLS [J].
HAUNER, H ;
PETRUSCHKE, T ;
GRIES, FA .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (02) :227-232