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脂联素是自然杀伤细胞细胞毒性的负调节因子。

Adiponectin is a negative regulator of NK cell cytotoxicity.

作者信息

Kim Kun-Yong, Kim Jae Kwang, Han Seung Hyun, Lim Jong-Seok, Kim Keun Il, Cho Dae Ho, Lee Myeong-Sok, Lee Jeong-Hyung, Yoon Do-Young, Yoon Suk Ran, Chung Jin Woong, Choi Inpyo, Kim Eunjoon, Yang Young

机构信息

Laboratory of Molecular and Cellular Biology, Department of Life Science, Sookmyung Women's University, Seoul 140-742, Korea.

出版信息

J Immunol. 2006 May 15;176(10):5958-64. doi: 10.4049/jimmunol.176.10.5958.

DOI:10.4049/jimmunol.176.10.5958
PMID:16670304
Abstract

NK cells are a key component of innate immune systems, and their activity is regulated by cytokines and hormones. Adiponectin, which is secreted from white adipose tissues, plays important roles in various diseases, including hypertension, cardiovascular diseases, inflammatory disorders, and cancer. In this study the effect of adiponectin on NK cell activity was investigated. Adiponectin was found to suppress the IL-2-enhanced cytotoxic activity of NK cells without affecting basal NK cell cytotoxicity and to inhibit IL-2-induced NF-kappaB activation via activation of the AMP-activated protein kinase, indicating that it suppresses IL-2-enhanced NK cell cytotoxicity through the AMP-activated protein kinase-mediated inhibition of NF-kappaB activation. IFN-gamma enhances NK cell cytotoxicity by causing an increase in the levels of expression of TRAIL and Fas ligand. The production of IFN-gamma, one of the NF-kappaB target genes in NK cells, was also found to be suppressed by adiponectin, accompanied by the subsequent down-regulation of IFN-gamma-inducible TRAIL and Fas ligand expression. These results clearly demonstrate that adiponectin is a potent negative regulator of IL-2-induced NK cell activation and thus may act as an in vivo regulator of anti-inflammatory functions.

摘要

自然杀伤细胞是先天性免疫系统的关键组成部分,其活性受细胞因子和激素调节。脂联素由白色脂肪组织分泌,在包括高血压、心血管疾病、炎症性疾病和癌症在内的各种疾病中发挥重要作用。在本研究中,研究了脂联素对自然杀伤细胞活性的影响。发现脂联素可抑制白细胞介素-2增强的自然杀伤细胞的细胞毒性活性,而不影响基础自然杀伤细胞的细胞毒性,并通过激活AMP激活的蛋白激酶抑制白细胞介素-2诱导的核因子κB激活,表明它通过AMP激活的蛋白激酶介导的核因子κB激活抑制来抑制白细胞介素-2增强的自然杀伤细胞细胞毒性。干扰素-γ通过导致肿瘤坏死因子相关凋亡诱导配体(TRAIL)和Fas配体表达水平增加来增强自然杀伤细胞的细胞毒性。还发现脂联素可抑制自然杀伤细胞中核因子κB靶基因之一干扰素-γ的产生,并随后下调干扰素-γ诱导的TRAIL和Fas配体表达。这些结果清楚地表明,脂联素是白细胞介素-2诱导的自然杀伤细胞激活的有效负调节因子,因此可能作为体内抗炎功能的调节因子发挥作用。

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