Jiang Hong, Zhang Xiaoyu, Lin Hening
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA.
Howard Hughes Medical Institute, Cornell University, Ithaca, NY 14853, USA.
Sci Rep. 2016 Apr 15;6:24371. doi: 10.1038/srep24371.
Tumor necrosis factor-α (TNF-α) is a proinflammation cytokine secreted by various cells. Understanding its secretive pathway is important to understand the biological functions of TNF-α and diseases associated with TNF-α. TNF-α is one of the first proteins known be modified by lysine fatty acylation (e.g. myristoylation). We previously demonstrated that SIRT6, a member of the mammalian sirtuin family of enzymes, can remove the fatty acyl modification on TNF-α and promote its secretion. However, the mechanistic details about how lysine fatty acylation regulates TNF-α secretion have been unknown. Here we present experimental data supporting that lysine fatty acylation promotes lysosomal targeting of TNF-α. The result is an important first step toward understanding the biological functions of lysine fatty acylation.
肿瘤坏死因子-α(TNF-α)是一种由多种细胞分泌的促炎细胞因子。了解其分泌途径对于理解TNF-α的生物学功能以及与TNF-α相关的疾病至关重要。TNF-α是最早已知可通过赖氨酸脂肪酰化修饰(如肉豆蔻酰化)的蛋白质之一。我们之前证明,哺乳动物沉默调节蛋白家族的成员SIRT6可以去除TNF-α上的脂肪酰基修饰并促进其分泌。然而,赖氨酸脂肪酰化如何调节TNF-α分泌的机制细节尚不清楚。在此,我们提供了实验数据,支持赖氨酸脂肪酰化促进TNF-α靶向溶酶体。这一结果是迈向理解赖氨酸脂肪酰化生物学功能的重要第一步。