Division of Endocrinology, Department of Medicine, Stanford University Medical Center, CA 94305, USA.
Diab Vasc Dis Res. 2010 Oct;7(4):311-8. doi: 10.1177/1479164110386126. Epub 2010 Oct 20.
We recently reported that a preponderance of small adipose cells, decreased expression of cell differentiation markers, and enhanced inflammatory activity in human subcutaneous whole adipose tissue were associated with insulin resistance. To test the hypothesis that small adipocytes exhibited these differential properties, we characterised small adipocytes from epididymal adipose tissue of Zucker Obese (ZO) and Lean (ZL) rats. Rat epididymal fat pads were removed and adipocytes isolated by collagenase digestion. Small adipocytes were separated by sequential filtration through nylon meshes. Adipocytes were fixed in osmium tetroxide for cell size distribution analysis via Beckman Coulter Multisizer. Quantitative real-time PCR for cell differentiation and inflammatory genes was performed. Small adipocytes represented a markedly greater percentage of the total adipocyte population in ZO than ZL rats (58±4% vs. 12±3%, p<0.001). In ZO rats, small as compared with total adipocytes had 4-fold decreased adiponectin, and 4-fold increased visfatin and IL-6 levels. Comparison of small adipocytes in ZO versus ZL rats revealed 3-fold decreased adiponectin and PPARγ levels, and 2.5-fold increased IL-6. In conclusion, ZO rat adipose tissue harbours a large proportion of small adipocytes that manifest impaired cell differentiation and pro-inflammatory activity, two mechanisms by which small adipocytes may contribute to insulin resistance.
我们最近报道,人体皮下全脂肪组织中小脂肪细胞的增多、细胞分化标志物表达的减少以及炎症活性的增强与胰岛素抵抗有关。为了验证小脂肪细胞具有这些差异特性的假设,我们对 Zucker 肥胖(ZO)和 Lean(ZL)大鼠的附睾脂肪组织中的小脂肪细胞进行了特征分析。从大鼠附睾脂肪垫中取出脂肪组织,并用胶原酶消化法分离脂肪细胞。通过尼龙滤网的连续过滤将小脂肪细胞分离出来。用锇四氧化物固定脂肪细胞,通过贝克曼库尔特 Multisizer 进行细胞大小分布分析。对细胞分化和炎症基因进行了定量实时 PCR 分析。与 ZL 大鼠相比,ZO 大鼠的总脂肪细胞中小脂肪细胞的比例明显更高(58±4%对 12±3%,p<0.001)。与总脂肪细胞相比,ZO 大鼠的小脂肪细胞中脂联素减少了 4 倍,而内脂素和 IL-6 水平则增加了 4 倍。与 ZO 大鼠相比,ZO 大鼠的小脂肪细胞中脂联素和 PPARγ水平降低了 3 倍,而 IL-6 水平则增加了 2.5 倍。总之,ZO 大鼠的脂肪组织中存在大量的小脂肪细胞,这些小脂肪细胞表现出细胞分化受损和促炎活性增强的特征,这两种机制可能导致小脂肪细胞引起胰岛素抵抗。