NEU1唾液酸酶通过NF-&kgr;B途径控制3T3-L1脂肪细胞中IL-6和MCP-1的基因表达和分泌

Y. Natori, M. Nasui, K. Edo, Shogo Sato, T. Sakurai, T. Kizaki, F. Kihara-Negishi
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引用次数: 15

摘要

唾液酸酶NEU1从糖缀合物中去除唾液酸,与多种细胞功能有关。异常的NEU1活性与多种病理相关,包括溶酶体贮积障碍、唾液中毒、自身免疫性疾病以及癌细胞的恶性和转移。我们最近报道了NEU1活性在3T3-L1脂肪形成过程中增加,并且在肥胖和糖尿病小鼠的附睾脂肪中更高。然而,NEU1在脂肪细胞中的确切功能尚未阐明。转染siRNA敲低3T3-L1脂肪细胞NEU1可显著降低LPS诱导的IL-6和MCP-1 mRNA表达和蛋白分泌。在转染了靶向NEU1(siNEU1)的siRNA序列的脂肪细胞中,IL-6和MCP-1的启动子活性以及核因子κB (NF-κB)核易位降低。使用siNEU1抑制NEU1会影响TLR4唾液化。这些发现表明NEU1可能通过TLR4/NF-κB信号通路参与脂肪细胞中IL-6和MCP-1的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NEU1 sialidase controls gene expression and secretion of IL-6 and MCP-1 through NF-&kgr;B pathway in 3T3-L1 adipocytes
A sialidase NEU1 that removes sialic acids from glycoconjugates has been implicated in diverse cellular functions. Aberrant NEU1 activity is associated with various pathologies including lysosomal storage disorder sialidosis, autoimmune diseases and the malignancy and metastasis of cancer cells. We recently reported that NEU1 activity increases during 3T3-L1 adipogenesis and that it is higher in the epididymal fat of obese and diabetic mice. However, the precise functions of NEU1 in adipocytes have not been elucidated. Knockdown of NEU1 using siRNA transfection in 3T3-L1 adipocytes significantly decreased the mRNA expression and protein secretion of IL-6 and MCP-1 induced by LPS. The promoter activities of both IL-6 and MCP-1 as well as nuclear factor-kappa B (NF-κB) nuclear translocation were reduced in adipocytes transfected with an siRNA sequence that targets NEU1(siNEU1). NEU1 suppression using siNEU1 affected TLR4 sialylation. These findings suggest that NEU1 is involved in the production of IL-6 and MCP-1 in adipocytes possibly through TLR4/NF-κB signalling.
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