Literature DB >> 9418955

Do olfactory glia have advantages over Schwann cells for CNS repair?

R J Franklin1, S C Barnett.   

Abstract

To a large extent the success of axon regeneration and sustained remyelination which distinguishes the PNS from the CNS is attributable to differences in their respective glial environments. For this reason, many have been attracted to the idea that repair of the CNS might be achieved by transplanting Schwann cells into areas of CNS pathology. Schwann cells will not only promote regeneration but will also myelinate axons thereby making them an appropriate cell type to mediate repair of lesions characterised by demyelination as well as axotomy. The recent discovery that olfactory glia are capable of forming myelin sheaths, together with their well-documented ability to support axon regeneration, means that these cells have a range of repair properties similar to that of Schwann cells. It is not clear at present which of these two alternatives, the Schwann cells or the olfactory glial cell, would be of greater benefit for achieving regeneration of axons or remyelination of persistent demyelination following transplantation into the CNS. In this article we review the repair properties of olfactory glia and identify the areas in which their use for repairing the CNS may have advantages over Schwann cells.

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Year:  1997        PMID: 9418955     DOI: 10.1002/(SICI)1097-4547(19971201)50:5<665::AID-JNR4>3.0.CO;2-F

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  17 in total

Review 1.  The transitional zone and CNS regeneration.

Authors:  J P Fraher
Journal:  J Anat       Date:  1999-02       Impact factor: 2.610

2.  Cell type- and isotype-specific expression and regulation of β-tubulins in primary olfactory ensheathing cells and Schwann cells in vitro.

Authors:  Mohamed Omar; Florian Hansmann; Robert Kreutzer; Mihaela Kreutzer; Gudrun Brandes; Konstantin Wewetzer
Journal:  Neurochem Res       Date:  2013-02-22       Impact factor: 3.996

3.  CNS Schwann cells display oligodendrocyte precursor-like potassium channel activation and antigenic expression in vitro.

Authors:  Kristel Kegler; Ilka Imbschweiler; Reiner Ulrich; Peter Kovermann; Christoph Fahlke; Ulrich Deschl; Arno Kalkuhl; Wolfgang Baumgärnter; Konstantin Wewetzer
Journal:  J Neural Transm (Vienna)       Date:  2014-02-01       Impact factor: 3.575

4.  Hepatocyte growth factor is a mitogen for olfactory ensheathing cells.

Authors:  H Yan; X Nie; J D Kocsis
Journal:  J Neurosci Res       Date:  2001-11-15       Impact factor: 4.164

Review 5.  Transplantation-mediated strategies to promote axonal regeneration following spinal cord injury.

Authors:  Xiao-Ming Xu; Stephen M Onifer
Journal:  Respir Physiol Neurobiol       Date:  2009-08-07       Impact factor: 1.931

Review 6.  Cell Therapeutic Strategies for Spinal Cord Injury.

Authors:  Pinghui Zhou; Jingjing Guan; Panpan Xu; Jingwen Zhao; Changchun Zhang; Bin Zhang; Yingji Mao; Wenguo Cui
Journal:  Adv Wound Care (New Rochelle)       Date:  2019-10-16       Impact factor: 4.730

7.  Schwann cells are removed from the spinal cord after effecting recovery from paraplegia.

Authors:  L Jasmin; G Janni; T M Moallem; D A Lappi; P T Ohara
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

8.  Subcellular localization of Mayven following expression of wild type and mutant EGFP tagged cDNAs.

Authors:  Paul Montague; Peter G E Kennedy; Susan C Barnett
Journal:  BMC Neurosci       Date:  2010-05-26       Impact factor: 3.288

Review 9.  Axons and glial interfaces: ultrastructural studies.

Authors:  John Fraher
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

Review 10.  Therapeutic potential of olfactory ensheathing cells in neurodegenerative diseases.

Authors:  Shao-Chih Chiu; Huey-Shan Hung; Shinn-Zong Lin; Esheral Chiang; Demeral David Liu
Journal:  J Mol Med (Berl)       Date:  2009-09-10       Impact factor: 4.599

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