Gene network underlying the glial regenerative response to central nervous system injury

被引:20
|
作者
Kato, Kentaro [1 ]
Losada-Perez, Maria [2 ]
Hidalgo, Alicia [3 ]
机构
[1] Kyorin Univ, Sch Med, Tokyo, Japan
[2] CSIC, Inst Cajal, Madrid, Spain
[3] Univ Birmingham, Sch Biosci, Birmingham, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
CNS; Drosophila; glia; repair; regeneration; injury; OPC; astrocyte; NG2; Kon-tiki; Prospero; Prox1; Notch; NFB; TNF; Eiger; OLIGODENDROCYTE PRECURSOR CELLS; JNK SIGNALING PATHWAY; AXON DEGENERATION; MULTIPLE-SCLEROSIS; DROSOPHILA MODEL; ADULT BRAIN; CNS; NG2; PROLIFERATION; ASTROCYTES;
D O I
10.1002/dvdy.24565
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Although the central nervous system does not regenerate, injury induces repair and regenerative responses in glial cells. In mammals, activated microglia clear up apoptotic cells and debris resulting from the injury, astrocytes form a scar that contains the lesion, and NG2-glia elicit a prominent regenerative response. NG2-glia regenerate themselves and differentiate into oligodendrocytes, which remyelinate axons leading to some recovery of locomotion. The regenerative response of glial cells is evolutionarily conserved across the animals and Drosophila genetics revealed an underlying gene network. This involves the genes Notch, kon-tiki, eiger, dorsal, and prospero, homologues of mammalian Notch1, ng2, TNF, NFB, and prox1, respectively. Feedback loops between these genes enable a surge in proliferation in response to injury and ensuing differentiation. Negative feedback sets a timer for proliferation, and prevents uncontrolled growth that could lead to glioma. Remarkable parallels are found in these genetic relationships between fruit flies and mammals. Drosophila findings provide insights into gene functions that could be manipulated in stem cells and progenitors for therapeutic repair. Developmental Dynamics 247:85-93, 2018. (c) 2017 Wiley Periodicals, Inc.
引用
收藏
页码:85 / 93
页数:9
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