脂肪组织
脂肪细胞
内科学
内分泌学
胰岛素抵抗
生物
基因表达
免疫组织化学
基因
微阵列
电池类型
脂肪生成
微阵列分析技术
细胞
肥胖
医学
遗传学
作者
Margareta Jernås,Jenny Palming,Kajsa Sjöholm,Eva Jennische,Per‐Arne Svensson,Britt G. Gabrielsson,Max Levin,Anders Sjögren,Mats Rudemo,Theodore C. Lystig,Björn Carlsson,Lena Carlsson,Malin Lönn,Margareta Jernås,Jenny Palming,Kajsa Sjöholm,Eva Jennische,Per‐Arne Svensson,Britt G. Gabrielsson,Max Levin
标识
DOI:10.1096/fj.05-5678fje
摘要
Enlarged adipocytes are associated with insulin resistance and are an independent predictor of type 2 diabetes. To understand the molecular link between these diseases and adipocyte hypertrophy, we developed a technique to separate human adipocytes from an adipose tissue sample into populations of small cells (mean 57.6+/-3.54 microm) and large cells (mean 100.1+/-3.94 microm). Microarray analysis of the cell populations separated from adipose tissue from three subjects identified 14 genes, of which five immune-related, with more than fourfold higher expression in large cells than small cells. Two of these genes were serum amyloid A (SAA) and transmembrane 4 L six family member 1 (TM4SF1). Real-time RT-PCR analysis of SAA and TM4SF1 expression in adipocytes from seven subjects revealed 19-fold and 22-fold higher expression in the large cells, respectively, and a correlation between adipocyte size and both SAA and TM4SF1 expression. The results were verified using immunohistochemistry. In comparison with 17 other human tissues and cell types by microarray, large adipocytes displayed by far the highest SAA and TM4SF1 expression. Thus, we have identified genes with markedly higher expression in large, compared with small, human adipocytes. These genes may link hypertrophic obesity to insulin resistance/type 2 diabetes.
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