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人诱导多能干细胞源性少突胶质前体细胞在脱髓鞘疾病中的旅程:从生成到移植。

The Journey of iPSC-derived OPCs in Demyelinating Disorders: From Generation to Transplantation.

机构信息

Student Research Committee, Babol University of Medical Science, Babol, Iran.

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Science, Babol, Iran.

出版信息

Curr Neuropharmacol. 2023;21(9):1980-1991. doi: 10.2174/1570159X21666230220150010.

Abstract

Loss of myelination is common among neurological diseases. It causes significant disability, even death, if it is not treated instantly. Different mechanisms involve the pathophysiology of demyelinating diseases, such as genetic background, infectious, and autoimmune inflammation. Recently, regenerative medicine and stem cell therapy have shown to be promising for the treatment of demyelinating disorders. Stem cells, including embryonic stem cells (ESCs), induced pluripotent stem cells (iPSCs), and adult stem cells (ASCs), can differentiate into oligodendrocyte progenitor cells (OPCs), which may convert to oligodendrocytes (OLs) and recover myelination. IPSCs provide an endless source for OPCs generation. However, the restricted capacity of proliferation, differentiation, migration, and myelination of iPSC-derived OPCs is a notable gap for future studies. In this article, we have first reviewed stem cell therapy in demyelinating diseases. Secondly, methods of different protocols have been discussed among and studies on iPSC-derived OPCs to contrast OPCs' transplantation efficacy. Lastly, we have reviewed the results of iPSCs-derived OLs production in each demyelination model.

摘要

脱髓鞘是常见的神经疾病。如果不及时治疗,它会导致严重的残疾甚至死亡。脱髓鞘疾病的病理生理学涉及多种机制,如遗传背景、感染和自身免疫炎症。最近,再生医学和干细胞疗法已显示出在治疗脱髓鞘疾病方面具有广阔的应用前景。干细胞,包括胚胎干细胞(ESCs)、诱导多能干细胞(iPSCs)和成人干细胞(ASCs),可以分化为少突胶质前体细胞(OPCs),后者可能转化为少突胶质细胞(OLs)并恢复髓鞘形成。iPSCs 为 OPCs 的产生提供了源源不断的来源。然而,iPSC 衍生的 OPCs 在增殖、分化、迁移和髓鞘形成方面的受限能力是未来研究的一个显著差距。在本文中,我们首先回顾了干细胞疗法在脱髓鞘疾病中的应用。其次,我们讨论了不同方案的方法,比较了 iPSC 衍生的 OPCs 在不同研究中的移植效果。最后,我们回顾了 iPSCs 衍生的 OLs 在每种脱髓鞘模型中的产生结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8517/10514531/5bddabaedcbb/CN-21-1980_F1.jpg

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