Sabelström Hanna, Stenudd Moa, Frisén Jonas
Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Exp Neurol. 2014 Oct;260:44-9. doi: 10.1016/j.expneurol.2013.01.026. Epub 2013 Jan 30.
Spinal cord injury results in cell loss, disruption of neural circuitry and chronic functional impairment. Several different cell types generate progeny in response to injury, which participate in scar formation and remyelination. Work over the last few years has identified neural stem cells and delineated the stem cell potential of different cell populations in the adult spinal cord under homeostasis and in response to injury. Neural stem cell properties are contained within the ependymal cell population, and these cells generate the majority of new astrocytes forming the glial scar. Oligodendrocyte progenitors give rise to myelinating oligodendrocytes in the intact spinal cord. They also generate the majority of remyelinating oligodendrocytes after spinal cord injury, with a minor contribution by ependymal cells. The fibrotic component of the scar tissue is generated by a subtype of pericytes. A better understanding of the regulation and precise function of different cells in the response to injury may aid in the development of regenerative strategies.
脊髓损伤会导致细胞丢失、神经回路破坏以及慢性功能障碍。几种不同类型的细胞会对损伤产生反应并产生子代细胞,这些子代细胞参与瘢痕形成和髓鞘再生。过去几年的研究已经鉴定出神经干细胞,并描绘了成年脊髓在稳态和损伤反应下不同细胞群体的干细胞潜能。神经干细胞特性存在于室管膜细胞群体中,这些细胞产生构成胶质瘢痕的大部分新星形胶质细胞。少突胶质前体细胞在完整脊髓中产生有髓鞘的少突胶质细胞。脊髓损伤后,它们也产生大部分参与髓鞘再生的少突胶质细胞,室管膜细胞的贡献较小。瘢痕组织的纤维化成分由周细胞的一个亚型产生。更好地理解不同细胞在损伤反应中的调控和精确功能可能有助于再生策略的开发。