双特异性磷酸酶在糖尿病肾病中的研究进展

Research Progress of Dual-Specificity Phosphatase in Diabetic Nephropathy

  • 摘要: 糖尿病肾病(diabetic nephropathy, DN) 作为糖尿病的一种常见微血管并发症, 已成为全球范围内终末期肾病的主要诱因。近年来, 针对双特异性磷酸酶(dual specific phosphatase, DUSP)家族成员的深入研究发现, DUSP在肾脏疾病状态下的表达水平显著降低, 推测增强其表达可减轻或改善肾脏疾病症状。DUSP主要功能为介导丝裂原活化蛋白激酶(mitogen-activated protein kinase, MAPK)去磷酸化过程, 从而有效抑制MAPK通路的活化, 对DN发生与发展发挥重要调控作用。本文旨在深入探讨MAPK与DN和DUSP的相关性, 并对DUSP在DN领域的研究进展进行总结, 以期为DN诊治提供新视角和重要理论依据。

     

    Abstract: Diabetic nephropathy(DN), a prevalent microvascular complication of diabetes, has emerged as a leading cause of end-stage renal disease worldwide. Recent studies on the dual-specific phosphatase (DUSP) family have revealed a significant reduction in DUSP expression levels in renal disease, suggesting that enhancing its expression may mitigate or alleviate the symptoms associated with renal disease. The primary function of DUSP is to mediate the dephosphorylation of mitogen-activated protein kinase (MAPK), which effectively inhibits the activation of the MAPK pathway, thus playing a crucial regulatory role in the onset and progression of DN. This article aims to investigate the correlation between DN and DUSP and to summarize the current research advancements concerning DUSP in the context of DN, providing new insights and essential theoretical foundations for its diagnosis and treatment.

     

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