New insights into glial scar formation after spinal cord injury

被引:114
作者
Tran, Amanda Phuong [1 ]
Warren, Philippa Mary [2 ]
Silver, Jerry [3 ]
机构
[1] Seattle Childrens Res Inst, Ctr Integrat Brain Res, Seattle, WA USA
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Wolfson Ctr Age Related Dis, Guys Campus, London, England
[3] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
基金
英国医学研究理事会;
关键词
Glia; Glial scar; Glial scar formation; Spinal cord injury; Chondroitin sulfate proteoglycans; Single-cell RNA sequencing; CHONDROITIN SULFATE PROTEOGLYCAN; RECEPTOR PTP-SIGMA; PROMOTES FUNCTIONAL RECOVERY; MEDIATED AXONAL DIEBACK; REGENERATION FAILURE; PERINEURONAL NETS; CNS INJURY; STEM-CELLS; REACTIVE ASTROGLIOSIS; CORTICOSPINAL AXONS;
D O I
10.1007/s00441-021-03477-w
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Severe spinal cord injury causes permanent loss of function and sensation throughout the body. The trauma causes a multifaceted torrent of pathophysiological processes which ultimately act to form a complex structure, permanently remodeling the cellular architecture and extracellular matrix. This structure is traditionally termed the glial/fibrotic scar. Similar cellular formations occur following stroke, infection, and neurodegenerative diseases of the central nervous system (CNS) signifying their fundamental importance to preservation of function. It is increasingly recognized that the scar performs multiple roles affecting recovery following traumatic injury. Innovative research into the properties of this structure is imperative to the development of treatment strategies to recover motor function and sensation following CNS trauma. In this review, we summarize how the regeneration potential of the CNS alters across phyla and age through formation of scar-like structures. We describe how new insights from next-generation sequencing technologies have yielded a more complex portrait of the molecular mechanisms governing the astrocyte, microglial, and neuronal responses to injury and development, especially of the glial component of the scar. Finally, we discuss possible combinatorial therapeutic approaches centering on scar modulation to restore function after severe CNS injury.
引用
收藏
页码:319 / 336
页数:18
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