Nephrology Department, Second Xiangya Hospital, Central South University, No. 139 Renmin Road, Changsha, 410011, Hunan, People's Republic of China.
Inflammation. 2018 Feb;41(1):1-10. doi: 10.1007/s10753-017-0657-7.
SUV39H1, the histone methyltransferase (HMTase) of histone H3 lysine 9 trimethylation (H3K9me3), is a known transcriptional repressor of inflammatory genes. The effect of SUV39H1 on inflammatory gene promoters under high-glucose stimulation in vascular smooth muscle cells (VSMCs), macrophages, and cardiomyocytes has been studied, but how SUV39H1 functions in renal tubules under diabetic conditions is unclear. Renal biopsy specimens of ten diabetic nephropathy (DN) subjects and seven non-DN minimal change diseases (MCD) subjects were collected. SUV39H1, IL-6, and MCP-1 expression in renal tissues were measured using immunohistochemical, while SUV39H1, H3K9me3, IL-6, and MCP-1 in human proximal tubular epithelial cells (HK-2) under varying glucose conditions were assayed by Western blot and ELISA. SUV39H1 was overexpressed in HK-2 cells; the regulation of SUV39H1 and H3K9me3 on NF-κB, IL-6, MCP-1, caspase 3, and apoptosis was measured. SUV39H1 was expressed more in diabetic human renal tubules. HK-2 cells with high glucose up-regulated IL-6 and MCP-1 in a dose- and time-dependent manner, and SUV39H1 expression was reduced with greater glucose and prolonged stimulation. Expression of H3K9me3 was synchronized with SUV39H1. Moreover, overexpression of SUV39H1 in high glucose environment was accompanied with increased H3K9me3 and decreased inflammation and apoptosis. SUV39H1 dysregulation may be involved in DN progression. Overexpression of SUV39H1 may reduce renal inflammation and apoptosis via epigenetic modulation, thus plays a protective role in DN.
SUV39H1 是组蛋白 H3 赖氨酸 9 三甲基化(H3K9me3)的组蛋白甲基转移酶(HMTase),是炎症基因的已知转录抑制剂。已经研究了 SUV39H1 在高葡萄糖刺激下对血管平滑肌细胞(VSMCs)、巨噬细胞和心肌细胞中炎症基因启动子的影响,但在糖尿病条件下 SUV39H1 在肾小管中的作用尚不清楚。收集了 10 名糖尿病肾病(DN)患者和 7 名非 DN 微小病变疾病(MCD)患者的肾活检标本。使用免疫组织化学测量肾组织中的 SUV39H1、IL-6 和 MCP-1 表达,同时通过 Western blot 和 ELISA 测定不同葡萄糖条件下人近端肾小管上皮细胞(HK-2)中的 SUV39H1、H3K9me3、IL-6 和 MCP-1。在 HK-2 细胞中过表达 SUV39H1;测量 SUV39H1 和 H3K9me3 对 NF-κB、IL-6、MCP-1、caspase 3 和细胞凋亡的调节作用。在糖尿病人类肾小管中 SUV39H1 的表达增加。高葡萄糖以剂量和时间依赖的方式上调 HK-2 细胞中的 IL-6 和 MCP-1,并且随着葡萄糖增加和刺激延长,SUV39H1 表达减少。H3K9me3 的表达与 SUV39H1 同步。此外,在高葡萄糖环境中过表达 SUV39H1 伴随着 H3K9me3 的增加以及炎症和凋亡的减少。SUV39H1 失调可能与 DN 的进展有关。SUV39H1 的过表达可能通过表观遗传调节减少肾脏炎症和凋亡,从而在 DN 中发挥保护作用。