Literature DB >> 1374657

Reorganization of the ependyma during axolotl spinal cord regeneration: changes in intermediate filament and fibronectin expression.

C M O'Hara1, M W Egar, E A Chernoff.   

Abstract

Changes in intermediate filament content and extracellular matrix material showed that the injury response of ependymal cells in lesioned axolotl spinal cord involves an epithelial-to-mesenchymal transformation, and that fibrous astrocytes are excluded from the remodeling lesion site. Antibody localization was used to visualize cytokeratin-, vimentin-, and glial fibrillary acidic protein- (GFAP-) containing intermediate filaments, as well as the adhesive glycoprotein fibronectin. In normal axolotl spinal cord cytokeratins were found near the apical surface of the ependymal cells. Transmission electron microscopic examination suggested that these cytokeratins were in tonofilaments. Cytokeratin expression was lost and vimentin production was initiated in ependymal cells 2-3 weeks following spinal cord injury. There was a period of approximately 1-2 weeks when cytokeratins and vimentin were co-expressed in vivo. This co-expression was maintained in vitro by culture on a fibronectin-coated substratum. As the central canal reformed, vimentin expression was lost. Ependymal cells lacked GFAP intermediate filaments, but GFAP was present in fibrous astrocytes of the neuropil and white matter. Following injury, GFAP localization showed that fibrous astrocytes disappeared from the remodeling lesion site and reappeared only after the ependymal epithelium reformed and newly myelinated axons were found. Fibronectin expression closely followed the expression of vimentin during mesenchymal ependymal cell outgrowth. These results suggest that the ependymal cell outgrowth requires changes in cell shape followed by changes in production of extracellular matrix.

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Year:  1992        PMID: 1374657     DOI: 10.1002/aja.1001930202

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  25 in total

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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
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Review 3.  Don't fence me in: harnessing the beneficial roles of astrocytes for spinal cord repair.

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Journal:  Restor Neurol Neurosci       Date:  2008       Impact factor: 2.406

4.  Genes encoding giant danio and golden shiner ependymin.

Authors:  D S Adams; M Kiyokawa; M E Getman; V E Shashoua
Journal:  Neurochem Res       Date:  1996-03       Impact factor: 3.996

5.  Absence of gliosis in a teleost model of spinal cord regeneration.

Authors:  Antonia G Vitalo; Ruxandra F Sîrbulescu; Iulian Ilieş; Günther K H Zupanc
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2016-05-25       Impact factor: 1.836

6.  Spinal cord regeneration in Xenopus laevis.

Authors:  Gabriela Edwards-Faret; Rosana Muñoz; Emilio E Méndez-Olivos; Dasfne Lee-Liu; Victor S Tapia; Juan Larraín
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7.  Fgf-2 in astroglial cells during vertebrate spinal cord recovery.

Authors:  Gehan H Fahmy; Marie Z Moftah
Journal:  Front Cell Neurosci       Date:  2010-11-04       Impact factor: 5.505

8.  Ependyma: phylogenetic evolution of glial fibrillary acidic protein (GFAP) and vimentin expression in vertebrate spinal cord.

Authors:  G Bodega; I Suárez; M Rubio; B Fernández
Journal:  Histochemistry       Date:  1994-08

9.  Up-regulation of neural stem cell markers suggests the occurrence of dedifferentiation in regenerating spinal cord.

Authors:  Sally Walder; Fang Zhang; Patrizia Ferretti
Journal:  Dev Genes Evol       Date:  2003-11-08       Impact factor: 0.900

Review 10.  Stem cells in canine spinal cord injury--promise for regenerative therapy in a large animal model of human disease.

Authors:  Barbara G McMahill; Dori L Borjesson; Maya Sieber-Blum; Jan A Nolta; Beverly K Sturges
Journal:  Stem Cell Rev Rep       Date:  2015-02       Impact factor: 5.739

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