Departments of Medicine and.
Pathology, UT Health, San Antonio, Texas 78229.
J Biol Chem. 2019 Jun 14;294(24):9440-9460. doi: 10.1074/jbc.RA118.007023. Epub 2019 Apr 26.
S6 kinase acts as a driver for renal hypertrophy and matrix accumulation, two key pathologic signatures of diabetic nephropathy. As a post-translational modification, S6 kinase undergoes acetylation at the C terminus. The role of this acetylation to regulate kidney glomerular cell hypertrophy and matrix expansion is not known. In mesangial cells, high glucose decreased the acetylation and enhanced phosphorylation of S6 kinase and its substrates rps6 and eEF2 kinase that lead to dephosphorylation of eEF2. To determine the mechanism of S6 kinase deacetylation, we found that trichostatin A, a pan-histone deacetylase (HDAC) inhibitor, blocked all high glucose-induced effects. Furthermore, high glucose increased the expression and association of HDAC1 with S6 kinase. HDAC1 decreased the acetylation of S6 kinase and mimicked the effects of high glucose, resulting in mesangial cell hypertrophy and expression of fibronectin and collagen I (α2). In contrast, siRNA against HDAC1 inhibited these effects by high glucose. A C-terminal acetylation-mimetic mutant of S6 kinase suppressed high glucose-stimulated phosphorylation of S6 kinase, rps6 and eEF2 kinase, and inhibited the dephosphorylation of eEF2. Also, the acetylation mimetic attenuated the mesangial cell hypertrophy and fibronectin and collagen I (α2) expression. Conversely, an S6 kinase acetylation-deficient mutant induced all the above effects of high glucose. Finally, in the renal glomeruli of diabetic rats, the acetylation of S6 kinase was significantly reduced concomitant with increased HDAC1 and S6 kinase activity. In aggregate, our data uncovered a previously unrecognized role of S6 kinase deacetylation in high glucose-induced mesangial cell hypertrophy and matrix protein expression.
S6 激酶作为肾脏肥大和基质积累的驱动因子,这是糖尿病肾病的两个关键病理特征。作为一种翻译后修饰,S6 激酶在 C 端发生乙酰化。这种乙酰化调节肾脏肾小球细胞肥大和基质扩张的作用尚不清楚。在系膜细胞中,高葡萄糖降低 S6 激酶及其底物 rps6 和 eEF2 激酶的乙酰化并增强其磷酸化,导致 eEF2 的去磷酸化。为了确定 S6 激酶去乙酰化的机制,我们发现曲古抑菌素 A(一种组蛋白去乙酰化酶(HDAC)抑制剂)阻断了所有高葡萄糖诱导的作用。此外,高葡萄糖增加了 HDAC1 与 S6 激酶的表达和结合。HDAC1 降低了 S6 激酶的乙酰化,模拟了高葡萄糖的作用,导致系膜细胞肥大和纤维连接蛋白和胶原 I(α2)的表达。相反,高葡萄糖引起的这些作用被针对 HDAC1 的 siRNA 抑制。S6 激酶 C 端乙酰化模拟突变体抑制了 S6 激酶、rps6 和 eEF2 激酶的高葡萄糖刺激的磷酸化,并抑制了 eEF2 的去磷酸化。此外,乙酰化模拟减轻了系膜细胞肥大和纤维连接蛋白和胶原 I(α2)的表达。相反,S6 激酶乙酰化缺陷突变体诱导了高葡萄糖的所有上述作用。最后,在糖尿病大鼠的肾小球中,S6 激酶的乙酰化明显降低,同时 HDAC1 和 S6 激酶活性增加。总之,我们的数据揭示了 S6 激酶去乙酰化在高葡萄糖诱导的系膜细胞肥大和基质蛋白表达中的一个以前未被认识的作用。