Ito Ayaka, Suganami Takayoshi, Miyamoto Yoshihiro, Yoshimasa Yasunao, Takeya Motohiro, Kamei Yasutomi, Ogawa Yoshihiro
Department of Molecular Medicine and Metabolism, Medical Research Institute, Tokyo Medical and Dental University, and Department of Medicine, National Cardiovascular Center Hospital, Osaka, Japan.
J Biol Chem. 2007 Aug 31;282(35):25445-52. doi: 10.1074/jbc.M701549200. Epub 2007 Jul 3.
Monocyte chemoattractant protein-1 (MCP-1), an important chemokine whose expression is increased during the course of obesity, plays a role in macrophage infiltration into obese adipose tissue. This study was designed to elucidate the role of mitogen-activated protein kinase (MAPK) phosphatase-1 (MKP-1) in the induction of MCP-1 during the course of adipocyte hypertrophy. We examined the time course of MKP-1 and MCP-1 mRNA expression and extracellular signal-regulated kinase (ERK) phosphorylation in the adipose tissue from mice rendered mildly obese by a short term high fat diet. We also studied the role of MKP-1 in the induction of MCP-1 in 3T3-L1 adipocytes during the course of adipocyte hypertrophy. MCP-1 mRNA expression was increased, followed by ERK activation and down-regulation of MKP-1, an inducible dual specificity phosphatase to inactivate ERK, in the adipose tissue at the early stage of obesity induced by a short term high fat diet, when macrophages are not infiltrated. Down-regulation of MKP-1 preceded ERK activation and increased production of MCP-1 in 3T3-L1 adipocytes in vitro during the course of adipocyte hypertrophy. Adenovirus-mediated restoration of MKP-1 in hypertrophied 3T3-L1 adipocytes reduced the otherwise increased ERK phosphorylation, thereby leading to the significant reduction of MCP-1 mRNA expression. This study provides evidence that the down-regulation of MKP-1 is critical for increased production of MCP-1 during the course of adipocyte hypertrophy.
单核细胞趋化蛋白-1(MCP-1)是一种重要的趋化因子,其表达在肥胖过程中会升高,在巨噬细胞浸润至肥胖脂肪组织中发挥作用。本研究旨在阐明丝裂原活化蛋白激酶(MAPK)磷酸酶-1(MKP-1)在脂肪细胞肥大过程中诱导MCP-1产生的作用。我们检测了短期高脂饮食致轻度肥胖小鼠脂肪组织中MKP-1和MCP-1 mRNA表达以及细胞外信号调节激酶(ERK)磷酸化的时间进程。我们还研究了MKP-1在3T3-L1脂肪细胞肥大过程中诱导MCP-1产生的作用。在短期高脂饮食诱导肥胖的早期阶段,即巨噬细胞尚未浸润时,脂肪组织中MCP-1 mRNA表达增加,随后ERK激活,而可诱导的双特异性磷酸酶MKP-1下调,该酶可使ERK失活。在体外3T3-L1脂肪细胞肥大过程中,MKP-1下调先于ERK激活并增加MCP-1的产生。腺病毒介导的MKP-1在肥大的3T3-L1脂肪细胞中的恢复降低了原本增加的ERK磷酸化,从而导致MCP-1 mRNA表达显著降低。本研究提供了证据表明,MKP-1的下调在脂肪细胞肥大过程中对MCP-1产生增加至关重要。