Chiellini Chiara, Bertacca Anna, Novelli Silvia E, Görgün Cem Z, Ciccarone Annamaria, Giordano Antonio, Xu Haiyan, Soukas Alexander, Costa Mario, Gandini Daniele, Dimitri Roberto, Bottone Pietro, Cecchetti Paolo, Pardini Ennia, Perego Lucia, Navalesi Renzo, Folli Franco, Benzi Luca, Cinti Saverio, Friedman Jeffrey M, Hotamisligil Gökhan S, Maffei Margherita
Department of Endocrinology and Metabolism, University of Pisa, Pisa, Italy.
J Cell Physiol. 2002 Feb;190(2):251-8. doi: 10.1002/jcp.10061.
Increase in adipose mass results in obesity and modulation of several factors in white adipose tissue (WAT). Two important examples are tumor necrosis factor alpha (TNFalpha) and leptin, both of which are upregulated in adipose tissue in obesity. In order to isolate genes differentially expressed in the WAT of genetically obese db/db mice compared to their lean littermates, we performed RNA fingerprinting and identified haptoglobin (Hp), which is significantly upregulated in the obese animals. Hp is a glycoprotein induced by a number of cytokines, LPS (Lipopolysaccharide), and more generally by inflammation. A significant upregulation of WAT Hp expression was also evident in several experimental obese models including the yellow agouti (/) A(y), ob/ob and goldthioglucose-treated mice (10-, 8-, and 7-fold, respectively). To identify the potential signals for an increase in Hp expression in obesity, we examined leptin and TNFalpha in vivo. Wild type animals treated with recombinant leptin did not show any alteration in WAT Hp expression compared to controls that were food restricted to the level of intake of the treated animals. On the other hand, Hp expression was induced in mice transgenically expressing TNFalpha in adipose tissue. Finally, a significant downregulation of WAT Hp mRNA was observed in ob/ob mice deficient in TNFalpha function, when compared to the ob/ob controls. These results demonstrate that haptoglobin expression in WAT is increased in obesity in rodents and TNFalpha is an important signal for this regulation.
脂肪量增加会导致肥胖,并调节白色脂肪组织(WAT)中的多种因子。两个重要的例子是肿瘤坏死因子α(TNFα)和瘦素,在肥胖状态下,这两种因子在脂肪组织中均会上调。为了分离出与瘦的同窝仔相比,基因肥胖的db/db小鼠白色脂肪组织中差异表达的基因,我们进行了RNA指纹分析,并鉴定出触珠蛋白(Hp),其在肥胖动物中显著上调。Hp是一种由多种细胞因子、脂多糖(LPS)以及更普遍地由炎症诱导产生的糖蛋白。在包括黄刺鼠(/)A(y)、ob/ob和金硫葡萄糖处理的小鼠(分别为10倍、8倍和7倍)在内的几种实验性肥胖模型中,白色脂肪组织Hp表达的显著上调也很明显。为了确定肥胖中Hp表达增加的潜在信号,我们在体内检测了瘦素和TNFα。与食物摄入量限制在与经重组瘦素处理的动物相同水平的对照组相比,经重组瘦素处理的野生型动物白色脂肪组织Hp表达没有任何变化。另一方面,在脂肪组织中转基因表达TNFα的小鼠中诱导了Hp表达。最后,与ob/ob对照组相比,在缺乏TNFα功能的ob/ob小鼠中观察到白色脂肪组织Hp mRNA显著下调。这些结果表明,啮齿动物肥胖时白色脂肪组织中触珠蛋白表达增加,TNFα是这种调节的重要信号。