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利用内源性神经干细胞促进脊髓损伤恢复

Employing Endogenous NSCs to Promote Recovery of Spinal Cord Injury.

作者信息

Liu Sumei, Chen Zhiguo

机构信息

Cell Therapy Center, Beijing Institute of Geriatrics, Xuanwu Hospital, Capital Medical University, Beijing 100053, China.

Key Laboratory of Neurodegenerative Diseases, Ministry of Education, Beijing 100053, China.

出版信息

Stem Cells Int. 2019 May 5;2019:1958631. doi: 10.1155/2019/1958631. eCollection 2019.

Abstract

Endogenous neural stem cells (NSCs) exist in the central canal of mammalian spinal cords. Under normal conditions, these NSCs remain quiescent and express FoxJ1. After spinal cord injury (SCI), the endogenous NSCs of a heterogeneous nature are activated and proliferate and migrate towards the lesion site and mainly differentiate into astrocytes to repair the injured tissue. , spinal cord NSCs are multipotent and can differentiate into neurons, astrocytes, and oligodendrocytes. The altered microenvironments after SCI play key roles on the fate determination of activated NSCs, especially on the neuronal specification potential. Studies show that the activated spinal cord NSCs can generate interneurons when transplanted into the adult hippocampus. In addition, the spinal cord NSCs exhibit low immunogenicity in a transplantation context, thus implicating a promising therapeutic potential on SCI recovery. Here, we summarize the characteristics of spinal cord NSCs, especially their properties after injury. With a better understanding of endogenous NSCs under normal and SCI conditions, we may be able to employ endogenous NSCs for SCI repair in the future.

摘要

内源性神经干细胞(NSCs)存在于哺乳动物脊髓的中央管中。在正常情况下,这些神经干细胞保持静止并表达FoxJ1。脊髓损伤(SCI)后,异质性的内源性神经干细胞被激活、增殖并向损伤部位迁移,主要分化为星形胶质细胞以修复受损组织。脊髓神经干细胞具有多能性,可分化为神经元、星形胶质细胞和少突胶质细胞。脊髓损伤后改变的微环境在激活的神经干细胞的命运决定中起关键作用,尤其是在神经元定向分化潜能方面。研究表明,激活的脊髓神经干细胞移植到成年海马体中时可产生中间神经元。此外,脊髓神经干细胞在移植环境中表现出低免疫原性,因此在脊髓损伤恢复方面具有广阔的治疗潜力。在此,我们总结脊髓神经干细胞的特征,尤其是其损伤后的特性。通过更好地了解正常和脊髓损伤条件下的内源性神经干细胞,我们未来或许能够利用内源性神经干细胞进行脊髓损伤修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91a/6525819/88a6c69fee20/SCI2019-1958631.001.jpg

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