Tu Chao, Wang Liangzhi, Wei Lan
Department of Internal Medicine, the Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, 213000, People's Republic of China.
Diabetes Metab Syndr Obes. 2022 May 4;15:1405-1412. doi: 10.2147/DMSO.S366403. eCollection 2022.
Diabetic microangiopathy is among the most common complications affecting patients with diabetes, and includes both diabetic retinopathy (DR) and diabetic nephropathy (DKD). Diabetic microangiopathy remains a persistent threat to the health and quality of life of affected patients. Mechanistically, the severity of DR and DKD is tied to mitochondrial and glucose metabolism abnormalities, with the activation of the glycolytic enzyme pyruvate kinase M2 (PKM2) contributing to mitochondrial and glomerular dysfunction, abnormal renal hemodynamics, and retinopathy. PKM2 can activate inflammatory bodies in macrophages to promote the release of inflammatory mediators, and serves as a key regulator of inflammatory factors, chemokines and adhesion molecules. As such, there is sufficient evidence that PKM2 can be used as a biomarker for the diagnosis of diabetes and diabetic microangiopathy. Here, we survey the mechanisms whereby PKM2 contributes to diabetes-related microvascular diseases, associated regulatory roles, post-translational modifications, and the potential utility of PKM2 as a therapeutic target. Through this literature review, we have determined that PKM2 offers promise as both a diagnostic marker and therapeutic target with direct relevance to research pertaining to diabetic microangiopathy.
糖尿病微血管病变是影响糖尿病患者的最常见并发症之一,包括糖尿病视网膜病变(DR)和糖尿病肾病(DKD)。糖尿病微血管病变仍然是影响患者健康和生活质量的持续威胁。从机制上讲,DR和DKD的严重程度与线粒体和葡萄糖代谢异常有关,糖酵解酶丙酮酸激酶M2(PKM2)的激活会导致线粒体和肾小球功能障碍、肾血流动力学异常以及视网膜病变。PKM2可激活巨噬细胞中的炎性小体,促进炎性介质的释放,并作为炎性因子、趋化因子和黏附分子的关键调节因子。因此,有充分证据表明PKM2可作为糖尿病和糖尿病微血管病变诊断的生物标志物。在此,我们综述了PKM2导致糖尿病相关微血管疾病的机制、相关调节作用、翻译后修饰以及PKM2作为治疗靶点的潜在效用。通过这篇文献综述,我们确定PKM2有望成为与糖尿病微血管病变相关研究直接相关的诊断标志物和治疗靶点。