Du Keyong, Murakami Shoko, Sun Yingmin, Kilpatrick Casey L, Luscher Bernhard
From the Molecular Oncology Research Institute, Tufts Medical Center, Boston, Massachusetts 02111 and
Department of Biochemistry and Molecular Biology.
J Biol Chem. 2017 Feb 17;292(7):2979-2991. doi: 10.1074/jbc.M116.747139. Epub 2017 Jan 5.
Insulin-dependent translocation of glucose transporter 4 (Glut4) to the plasma membrane plays a key role in the dynamic regulation of glucose homeostasis. We recently showed that this process is critically dependent on palmitoylation of Glut4 at Cys-223. To gain further insights into the regulation of Glut4 palmitoylation, we set out to identify the palmitoyl acyltransferase (PAT) involved. Here we report that among 23 mammalian DHHC proteins, DHHC7 is the major Glut4 PAT, based on evidence that ectopic expression of DHHC7 increased Glut4 palmitoylation, whereas DHHC7 knockdown in 3T3-L1 adipocytes and DHHC7 KO in adipose tissue and muscle decreased Glut4 palmitoylation. Moreover, inactivation of DHHC7 suppressed insulin-dependent Glut4 membrane translocation in both 3T3-L1 adipocytes and primary adipocytes. Finally, DHHC7 KO mice developed hyperglycemia and glucose intolerance, thereby confirming that DHHC7 represents the principal PAT for Glut4 and that this mechanism is essential for insulin-regulated glucose homeostasis.
胰岛素依赖的葡萄糖转运蛋白4(Glut4)向质膜的转位在葡萄糖稳态的动态调节中起关键作用。我们最近表明,这一过程严重依赖于Glut4在半胱氨酸-223处的棕榈酰化。为了进一步深入了解Glut4棕榈酰化的调节机制,我们着手鉴定相关的棕榈酰酰基转移酶(PAT)。在此我们报告,在23种哺乳动物DHHC蛋白中,DHHC7是主要的Glut4 PAT,依据如下:异位表达DHHC7可增加Glut4的棕榈酰化,而在3T3-L1脂肪细胞中敲低DHHC7以及在脂肪组织和肌肉中敲除DHHC7可降低Glut4的棕榈酰化。此外,DHHC7失活抑制了3T3-L1脂肪细胞和原代脂肪细胞中胰岛素依赖的Glut4膜转位。最后,DHHC7基因敲除小鼠出现高血糖和葡萄糖不耐受,从而证实DHHC7是Glut4的主要PAT,且该机制对于胰岛素调节的葡萄糖稳态至关重要。