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Molecular targeting regulation of proliferation and differentiation of the bone marrow-derived mesenchymal stem cells or mesenchymal stromal cells

机译:分子靶向调控骨髓源间充质干细胞或间质基质细胞的增殖和分化

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摘要

The bone marrow-derived mesenchymal stem cells or mesenchymal stromal cells (MSCs), with pluripotent differentiation capacity, present an ideal source for cell transplantation or tissue engineering therapies, but exact understanding of regulating mechanism underling MSC proliferation and differentiation remains a critical issue in securing their safe and efficient clinical application. This review outlines current knowledge regarding MSC cell surface biomarkers and molecular mechanisms of MSC differentiation and proliferation with emphasis on Wnt/β-catenin signaling, Notch signaling pathway, bone morphogenesis proteins and various growth factors functioning in regulation of differentiation and proliferation of MSCs. Possible relation of oncogene and immunosuppressive activities of MSCs with tumorigenicity or tumor generation is also addressed for safe translational clinical application. Fast increase of MSC knowledge and techniques has led to some successful clinical trials and helped devising new tissue engineering therapies for bone and cartilage diseases that severely afflict human health. Production of adult MSC-derived functional neurons can further extend their therapeutic application in nerve injury and neurodegenerative diseases. It is promising that MSCs shall overcome ethical and immunorejection problems appeared in human embryonic stem cells, and specific molecular targeting manipulation may result in practical MSC therapy for personalized treatment of various diseases in the regeneration medicine.
机译:骨髓来源的间充质干细胞或间充质基质细胞(MSCs)具有多能分化能力,是细胞移植或组织工程疗法的理想来源,但是准确了解调节MSC增殖和分化基础的调节机制仍然是确保安全的关键问题。其安全有效的临床应用。这篇综述概述了有关MSC细胞表面生物标志物和MSC分化和增殖的分子机制的当前知识,重点是Wnt /β-catenin信号传导,Notch信号传导途径,骨形态发生蛋白和各种调节MSC分化和增殖的生长因子。为了安全的翻译临床应用,还讨论了MSC的致癌基因和免疫抑制活性与致瘤性或肿瘤发生的可能关系。 MSC知识和技术的快速增长导致了一些成功的临床试验,并帮助设计出了新的组织工程疗法,用于严重危害人类健康的骨骼和软骨疾病。成人MSC衍生的功能神经元的生产可以进一步扩展其在神经损伤和神经退行性疾病中的治疗应用。 MSC有望克服人类胚胎干细胞中出现的伦理和免疫排斥问题,并且有针对性的分子靶向操作可能会产生实用的MSC疗法,用于个性化治疗再生医学中的各种疾病。

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