EphB Signaling Directs Peripheral Nerve Regeneration through Sox2-Dependent Schwann Cell Sorting

被引:437
作者
Parrinello, Simona [1 ,2 ]
Napoli, Ilaria [1 ,2 ]
Ribeiro, Sara [1 ,2 ]
Digby, Patrick Wingfield [1 ,2 ]
Fedorova, Marina [1 ,2 ]
Parkinson, David B. [3 ]
Doddrell, Robin D. S. [3 ]
Nakayama, Masanori [4 ,5 ]
Adams, Ralf H. [4 ,5 ]
Lloyd, Alison C. [1 ,2 ]
机构
[1] UCL, MRC Lab Mol Cell Biol, London WC1E 6BT, England
[2] UCL, UCL Canc Inst, London WC1E 6BT, England
[3] Univ Plymouth, Peninsula Coll Med & Dent, Plymouth PL6 8BU, Devon, England
[4] Univ Munster, Dept Tissue Morphogenesis, Max Planck Inst Mol Biomed, D-48149 Munster, Germany
[5] Univ Munster, Fac Med, D-48149 Munster, Germany
关键词
NEURAL CREST MIGRATION; N-CADHERIN; AXON; SYSTEM; FIBROBLASTS; PRECURSORS; EXPRESSION; PATTERNS; ADHESION; GUIDANCE;
D O I
10.1016/j.cell.2010.08.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peripheral nervous system has astonishing regenerative capabilities in that cut nerves are able to reconnect and re-establish their function. Schwann cells are important players in this process, during which they dedifferentiate to a progenitor/stem cell and promote axonal regrowth. Here, we report that fibroblasts also play a key role. Upon nerve cut, ephrin-B/EphB2 signaling between fibroblasts and Schwann cells results in cell sorting, followed by directional collective cell migration of Schwann cells out of the nerve stumps to guide regrowing axons across the wound. Mechanistically, we find that cell-sorting downstream of EphB2 is mediated by the stemness factor Sox2 through N-cadherin relocalization to Schwann cell-cell contacts. In vivo, loss of EphB2 signaling impaired organized migration of Schwann cells, resulting in misdirected axonal regrowth. Our results identify a link between Ephs and Sox proteins, providing a mechanism by which progenitor cells can translate environmental cues to orchestrate the formation of new tissue.
引用
收藏
页码:145 / 155
页数:11
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