Literature DB >> 12324218

Spinal cord regeneration: intrinsic properties and emerging mechanisms.

Ellen A G Chernoff1, Kazuna Sato, Angela Corn, Rachel E Karcavich.   

Abstract

Injured spinal cord regenerates in adult fish and urodele amphibians, young tadpoles of anuran amphibians, lizard tails, embryonic birds and mammals, and in adults of at least some strains of mice. The extent of this regeneration is described with respect to axonal regrowth, neurogenesis, glial responses, and maintenance of an 'embryonic' environment. The regeneration process in amphibian spinal cord demonstrates that gap replacement and caudal regeneration share some properties with developing spinal cord. This review considers the extent to which intrinsically regenerating spinal cord demonstrates neural stem cell behavior and to what extent anterior-posterior and dorsal-ventral patterning might be involved.

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Year:  2002        PMID: 12324218     DOI: 10.1016/s1084952102000927

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  10 in total

Review 1.  C. elegans as a genetic model to identify novel cellular and molecular mechanisms underlying nervous system regeneration.

Authors:  Hui Chiu; Amel Alqadah; Chiou-Fen Chuang; Chieh Chang
Journal:  Cell Adh Migr       Date:  2011 Sep-Oct       Impact factor: 3.405

2.  Dynamic membrane depolarization is an early regulator of ependymoglial cell response to spinal cord injury in axolotl.

Authors:  Keith Sabin; Tiago Santos-Ferreira; Jaclyn Essig; Sarah Rudasill; Karen Echeverri
Journal:  Dev Biol       Date:  2015-10-20       Impact factor: 3.582

3.  EST-based identification of genes expressed in brain and spinal cord of Gekko japonicus, a species demonstrating intrinsic capacity of spinal cord regeneration.

Authors:  Yan Liu; Fei Ding; Mei Liu; Maorong Jiang; Hui Yang; Xiao Feng; Xiaosong Gu
Journal:  J Mol Neurosci       Date:  2006       Impact factor: 3.444

4.  Enhanced de novo neurogenesis and dopaminergic neurogenesis in the substantia nigra of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced Parkinson's disease-like mice.

Authors:  Xiaoyang Shan; Liying Chi; Michael Bishop; Chun Luo; Lindsey Lien; Zheng Zhang; Rugao Liu
Journal:  Stem Cells       Date:  2006-01-19       Impact factor: 6.277

5.  Robust axonal growth and a blunted macrophage response are associated with impaired functional recovery after spinal cord injury in the MRL/MpJ mouse.

Authors:  S K Kostyk; P G Popovich; B T Stokes; P Wei; L B Jakeman
Journal:  Neuroscience       Date:  2008-08-19       Impact factor: 3.590

6.  Radial glial progenitors repair the zebrafish spinal cord following transection.

Authors:  Lisa K Briona; Richard I Dorsky
Journal:  Exp Neurol       Date:  2014-04-08       Impact factor: 5.330

7.  Structural and functional regeneration after spinal cord injury in the weakly electric teleost fish, Apteronotus leptorhynchus.

Authors:  Ruxandra F Sîrbulescu; Iulian Ilieş; Günther K H Zupanc
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2009-05-10       Impact factor: 1.836

8.  Spinal cord transection in the larval zebrafish.

Authors:  Lisa K Briona; Richard I Dorsky
Journal:  J Vis Exp       Date:  2014-05-21       Impact factor: 1.355

9.  Musashi and Plasticity of Xenopus and Axolotl Spinal Cord Ependymal Cells.

Authors:  Ellen A G Chernoff; Kazuna Sato; Hai V N Salfity; Deborah A Sarria; Teri Belecky-Adams
Journal:  Front Cell Neurosci       Date:  2018-02-27       Impact factor: 5.505

10.  AP-1cFos/JunB/miR-200a regulate the pro-regenerative glial cell response during axolotl spinal cord regeneration.

Authors:  Keith Z Sabin; Peng Jiang; Micah D Gearhart; Ron Stewart; Karen Echeverri
Journal:  Commun Biol       Date:  2019-03-06
  10 in total

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