Suppr超能文献

短期链脲佐菌素诱导糖尿病大鼠肾脏中错配修复基因的免疫组化表达模式。

Immunohistochemical Expression Pattern of Mismatch Repair Genes in the Short-term Streptozotocin-induced Diabetic Rat Kidneys.

机构信息

Intensive Care Unit, Department of Internal Medicine, University Hospital Centre Split.

Department of Anatomy, Histology and Embryology, University of Split School of Medicine, Split, Croatia.

出版信息

Appl Immunohistochem Mol Morphol. 2021 Oct 1;29(9):e83-e91. doi: 10.1097/PAI.0000000000000937.

Abstract

We studied the expression of mismatch repair genes (MMRs)-mutS protein homolog 2 (MSH2), PMS2, MutL homolog 1 (MLH1), and yH2AFX in diabetic rat kidneys. Streptozotocin-induced diabetes mellitus type 1 rat model (DM1) was used. Renal samples were collected 2 weeks and 2 months after DM1 induction and immunohistochemical expression of MMR genes in the renal cortex was analyzed. Diabetic animals showed lower MSH2 and higher yH2AFX kidney expression both 2 weeks and 2 months after DM1 induction. MLH1 expression significantly increased 2 weeks after DM1 induction (P<0.0001). The most substantial differences were observed in the period 2 weeks after induction, with lower MSH2 and higher MLH1 expression in the proximal convoluted tubules and distal convoluted tubules (DCT) of diabetic animals (P<0.001). yH2AFX expression significantly increased in the DCT of diabetic animals at both time points (P<0.001; P<0.01). PMS2 expression changed only in the glomeruli, where it significantly decreased 2 months after DM1 induction (P<0.05). We concluded that the most substantial changes in renal expression of MMRs are happening already 2 weeks after diabetes induction, predominantly in the proximal convoluted tubules and DCT. Moreover, DCT could have a critical role in the pathophysiology of diabetic nephropathy (DN) and might be a future therapeutic target in this condition. The obtained results point to the MMRs as a potential factor in the development and progression of DN, as well as the possible link between DN and renal carcinogenesis.

摘要

我们研究了错配修复基因(MMR)-MutS 蛋白同源物 2(MSH2)、PMS2、MutL 同源物 1(MLH1)和 yH2AFX 在糖尿病大鼠肾脏中的表达。使用链脲佐菌素诱导的 1 型糖尿病大鼠模型(DM1)。在 DM1 诱导后 2 周和 2 个月收集肾脏样本,并分析肾皮质中 MMR 基因的免疫组织化学表达。糖尿病动物在 DM1 诱导后 2 周和 2 个月时肾脏中 MSH2 表达降低,yH2AFX 表达升高。MLH1 表达在 DM1 诱导后 2 周时显著增加(P<0.0001)。在诱导后 2 周的时间段内观察到最显著的差异,糖尿病动物的近端曲管和远端曲管(DCT)中 MSH2 表达降低,MLH1 表达升高(P<0.001)。yH2AFX 表达在糖尿病动物的 DCT 中在两个时间点均显著增加(P<0.001;P<0.01)。PMS2 表达仅在肾小球中发生变化,在 DM1 诱导后 2 个月时显著降低(P<0.05)。我们得出结论,在糖尿病诱导后 2 周内,MMR 在肾脏中的表达发生了最显著的变化,主要发生在近端曲管和 DCT。此外,DCT 在糖尿病肾病(DN)的病理生理学中可能具有关键作用,并且可能成为该疾病的未来治疗靶点。研究结果表明,MMR 可能是 DN 发生和进展的潜在因素,以及 DN 与肾肿瘤发生之间的可能联系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验