Department of Molecular Biology, Hebei Key Lab of Laboratory Animal, Hebei Medical University, Shijiazhuang, China.
Mol Cell Endocrinol. 2013 Dec 5;381(1-2):255-60. doi: 10.1016/j.mce.2013.08.007. Epub 2013 Aug 22.
Although C-peptide has unique beneficial effects on diabetic nephropathy (DN), its functional localization and molecular mechanism have not been fully clarified. Whether C-peptide exhibits its protective role through the regulation of inducible nitric oxide synthase (iNOS), a key enzyme in oxidative stress, is not clear. In this study, it was revealed that C-peptide could enter the nucleus of high glucose-stimulated mesangial cells, especially in a time-dependent manner by high glucose pretreatment, while no C-peptide was detected in low glucose-cultured mesangial cells. The dynamic functional localization of C-peptide might be the intrinsic cause of its unique beneficial effects for DN, which may provide a foundation for further clarification of its underlying mechanism. Our preliminarily data also shown C-peptide suppressed the iNOS expression. Taking together, these results revealed the dynamic functional localization of C-peptide by high glucose stimulation in rat mesangial cells, which might suppress expression of iNOS to exhibit its protective effects.
虽然 C 肽对糖尿病肾病(DN)有独特的有益作用,但它的功能定位和分子机制尚未完全阐明。C 肽是否通过调节氧化应激中的关键酶诱导型一氧化氮合酶(iNOS)来发挥其保护作用尚不清楚。在这项研究中,研究揭示了 C 肽可以进入高糖刺激的系膜细胞的细胞核,特别是在高糖预处理时具有时间依赖性,而在低糖培养的系膜细胞中则检测不到 C 肽。C 肽的动态功能定位可能是其对 DN 独特有益作用的内在原因,这可能为进一步阐明其潜在机制提供基础。我们的初步数据还表明 C 肽抑制了 iNOS 的表达。综上所述,这些结果揭示了 C 肽在大鼠系膜细胞中受高糖刺激后的动态功能定位,可能通过抑制 iNOS 的表达来发挥其保护作用。