Song Min Jeong, Kim Kang Ho, Yoon Jeong Min, Kim Jae Bum
Department of Biological Sciences, Research Center for Functional Cellulomics, Seoul National University, Seoul 151-742, Republic of Korea.
Biochem Biophys Res Commun. 2006 Aug 4;346(3):739-45. doi: 10.1016/j.bbrc.2006.05.170. Epub 2006 Jun 6.
Chronic inflammation is closely associated with metabolic disorders such as obesity and type 2 diabetes, however, the underlying mechanism is unclear. Toll-like receptors (TLRs) play a key role in innate immune response as well as inflammatory signals. Here, we observed that mRNA level of TLR4 was induced during adipocyte differentiation and remarkably enhanced in fat tissues of obese db/db mice. In addition, activation of TLR4 with either LPS or free fatty acids stimulated NFkappaB signaling and expression of inflammatory cytokine genes, such as TNFalpha and IL-6 in 3T3-L1 adipocytes. Furthermore, we discovered that TLR4 activation in 3T3-L1 adipocytes provoked insulin resistance. Taken together, these results suggest that activation of TLR4 in adipocyte might be implicated in the onset of insulin resistance in obesity and type 2 diabetes.
慢性炎症与肥胖和2型糖尿病等代谢紊乱密切相关,然而,其潜在机制尚不清楚。Toll样受体(TLRs)在先天免疫反应以及炎症信号中起关键作用。在此,我们观察到TLR4的mRNA水平在脂肪细胞分化过程中被诱导,并且在肥胖的db/db小鼠的脂肪组织中显著增强。此外,用脂多糖(LPS)或游离脂肪酸激活TLR4可刺激3T3-L1脂肪细胞中的NFκB信号传导以及炎症细胞因子基因如TNFα和IL-6的表达。此外,我们发现3T3-L1脂肪细胞中TLR4的激活引发胰岛素抵抗。综上所述,这些结果表明脂肪细胞中TLR4的激活可能与肥胖和2型糖尿病中胰岛素抵抗的发生有关。