The activation of dormant ependymal cells following spinal cord injury

被引:4
|
作者
Rodriguez-Jimenez, Francisco Javier [1 ]
Jendelova, Pavla [3 ]
Erceg, Slaven [1 ,2 ,3 ]
机构
[1] Res Ctr Principe Felipe, Stem Cell Therapies Neurodegenerat Dis Lab, C Eduardo Primo Yufera 3, Valencia 46012, Spain
[2] Res Ctr Principe Felipe, Natl Stem Cell Bank Valencia Node, C Eduardo Primo Yufera 3, Valencia 46012, Spain
[3] Czech Acad Sci, Inst Expt Med, Dept Neuroregenerat, Prague, Czech Republic
关键词
Spinal cord injury; Ependymal cells; Activation; Regeneration; NEURAL STEM-CELLS; P2X7 RECEPTOR INHIBITION; CENTRAL-NERVOUS-SYSTEM; BRILLIANT-BLUE-G; NEURONAL DIFFERENTIATION; STEM/PROGENITOR CELLS; PURINERGIC RECEPTORS; ADHESION MOLECULE; IMPROVES RECOVERY; PROGENITOR CELLS;
D O I
10.1186/s13287-023-03395-4
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Ependymal cells, a dormant population of ciliated progenitors found within the central canal of the spinal cord, undergo significant alterations after spinal cord injury (SCI). Understanding the molecular events that induce ependymal cell activation after SCI represents the first step toward controlling the response of the endogenous regenerative machinery in damaged tissues. This response involves the activation of specific signaling pathways in the spinal cord that promotes self-renewal, proliferation, and differentiation. We review our current understanding of the signaling pathways and molecular events that mediate the SCI-induced activation of ependymal cells by focusing on the roles of some cell adhesion molecules, cellular membrane receptors, ion channels (and their crosstalk), and transcription factors. An orchestrated response regulating the expression of receptors and ion channels fine-tunes and coordinates the activation of ependymal cells after SCI or cell transplantation. Understanding the major players in the activation of ependymal cells may help us to understand whether these cells represent a critical source of cells contributing to cellular replacement and tissue regeneration after SCI. A more complete understanding of the role and function of individual signaling pathways in endogenous spinal cord progenitors may foster the development of novel targeted therapies to induce the regeneration of the injured spinal cord.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Central Canal Ependymal Cells Proliferate Extensively in Response to Traumatic Spinal Cord Injury but Not Demyelinating Lesions
    Lacroix, Steve
    Hamilton, Laura K.
    Vaugeois, Alexandre
    Beaudoin, Stefanny
    Breault-Dugas, Christian
    Pineau, Isabelle
    Levesque, Sebastien A.
    Gregoire, Catherine-Alexandra
    Fernandes, Karl J. L.
    PLOS ONE, 2014, 9 (01):
  • [32] Pain following spinal cord injury
    PJ Siddall
    JD Loeser
    Spinal Cord, 2001, 39 : 63 - 73
  • [33] Pain following spinal cord injury
    Defrin, R
    Ohry, A
    Blumen, N
    Urca, G
    SPINAL CORD, 2002, 40 (02) : 96 - 97
  • [34] Depression following a spinal cord injury
    Boekamp, JR
    Overholser, JC
    Schubert, DSP
    INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE, 1996, 26 (03): : 329 - 349
  • [35] Pain following spinal cord injury
    Gülçin Demirel
    Hürriyet Yllmaz
    Belgin Gençosmanoğlu
    Nur Kesiktaş
    Spinal Cord, 1998, 36 : 25 - 28
  • [36] Pain following spinal cord injury
    Siddall, PJ
    Loeser, JD
    SPINAL CORD, 2001, 39 (02) : 63 - 73
  • [37] Mortality following spinal cord injury
    Yeo, JD
    Walsh, J
    Rutkowski, S
    Soden, R
    Craven, M
    Middleton, J
    SPINAL CORD, 1998, 36 (05) : 329 - 336
  • [38] Pain following spinal cord injury
    Demirel, G
    Yllmaz, H
    Gencosmanoglu, B
    Kesiktas, N
    SPINAL CORD, 1998, 36 (01) : 25 - 28
  • [39] Pain following spinal cord injury
    R Defrin
    A Ohry
    N Blumen
    G Urca
    Spinal Cord, 2002, 40 : 96 - 97
  • [40] Mortality following spinal cord injury
    John D Yeo
    John Walsh
    Sue Rutkowski
    Ros Soden
    Mary Craven
    James Middleton
    Spinal Cord, 1998, 36 : 329 - 336