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Mesenchymal Stem Cells as Therapeutic Candidates for Halting the Progression of Diabetic Nephropathy

机译:间充质干细胞作为治疗糖尿病肾病进展的治疗候选者

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Mesenchymal stem cells (MSCs) possess pleiotropic properties that include immunomodulation, inhibition of apoptosis, fibrosis and oxidative stress, secretion of trophic factors, and enhancement of angiogenesis. These properties provide a broad spectrum for their potential in a wide range of injuries and diseases, including diabetic nephropathy (DN). MSCs are characterized by adherence to plastic, expression of the surface molecules CD73, CD90, and CD105 in the absence of CD34, CD45, HLA-DR, and CD14 or CD11b and CD79a or CD19 surface molecules, and multidifferentiation capacity in vitro. MSCs can be derived from many tissue sources, consistent with their broad, possibly ubiquitous distribution. This article reviews the existing literature and knowledge of MSC therapy in DN, as well as the most appropriate rodent models to verify the therapeutic potential of MSCs in DN setting. Some predinical relevant studies are highlighted and new perspectives of combined therapies for decreasing DN progression are discussed. Hence, improved comprehension and interpretation of experimental data will accelerate the progress towards clinical trials that should assess the feasibility and safety of this therapeutic approach in humans. Therefore, MSC-based therapies may bring substantial benefit for patients suffering from DN.
机译:间充质干细胞(MSCs)具有抗性特性,包括免疫调节,抑制凋亡,纤维化和氧化应激,营养因子的分泌,以及血管生成的增强。这些性质为其在广泛的伤害和疾病中提供了广泛的频谱,包括糖尿病肾病(DN)。 MSCs的特征在于在没有CD34,CD45,HLA-DR和CD14或CD11B和CD79A或CD79A或CD19表面分子的情况下粘附到塑料,表面分子CD73,CD90和CD105的表达,以及体外多草体能力。 MSC可以源自许多组织来源,符合其宽泛的,可能无处不在的分布。本文审查了DN中现有的文学和知识,以及最合适的啮齿动物模型,以验证DN设置中MSC的治疗潜力。讨论了一些突出的相关研究,并讨论了用于减少DN进展的组合疗法的新观点。因此,改善的理解和对实验数据的解释将加速对临床试验的进展,这些临床试验应该评估这种治疗方法在人类中的可行性和安全性。因此,基于MSC的疗法可能为患有DN的患者带来大量益处。

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