Expression profiling during adipocyte differentiation of 3T3-L1 fibroblasts

被引:56
作者
Jessen, BA [1 ]
Stevens, GJ [1 ]
机构
[1] Agouron Pharmaceut Inc, Drug Safety Evaluat, Pfizer Global Res & Dev, San Diego, CA 92121 USA
关键词
DNA microarray; 11 beta-hydroxysteroid dehydrogenase 1; lipocalin; 2; haptoglobin;
D O I
10.1016/S0378-1119(02)01017-X
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
The 3T3-L1 cell line is a well-established and commonly used in vitro model to assess adipocyte differentiation. Over the course of several days confluent 3T3-L1 cells can be converted to adipocytes in the presence of an adipogenic cocktail. Changes in gene expression were measured by DNA microarrays at three time points (24 h, 4 days, and I week) during the course of differentiation from preadipocytes to mature adipocytes. Several functional categories of genes were affected by adipocyte conversion. In addition, seven genes were found to be commonly altered by 5-fold or more by adipocyte conversion at all three time points. Lipocalin 2, haptoglobin, serum amyloid A3, stearoyl-CoA desaturase, and 11beta-hydroxysteroid dehydrogenase 1 were induced while actin alpha2 and procollagen VIII alpha1 were suppressed by adipocyte differentiation. Further study of the regulation of these genes and pathways will lead to an increased understanding of the biochemical pathways involved in adipocyte differentiation and possibly to the identification of new therapeutic targets for treatment of obesity and other metabolic diseases. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:95 / 100
页数:6
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