Literature DB >> 12503086

Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity.

Paul A Rosenberg1, Weimin Dai, Xiao Dong Gan, Sanjida Ali, Jennifer Fu, Stephen A Back, Russell M Sanchez, Michael M Segal, Pamela L Follett, Frances E Jensen, Joseph J Volpe.   

Abstract

We examined the vulnerability to excitotoxicity of rat oligodendrocytes in dissociated cell culture at different developmental stages. Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lineage were vulnerable to this insult. To test the hypothesis that the sensitivity of immature oligodendrocytes and the resistance of mature oligodendrocytes to kainate toxicity were due to differences in membrane responsiveness to kainate, we used whole-cell patch-clamp recording. Oligodendrocyte precursors in cultures vulnerable to kainate toxicity responded to 500 microM kainate with large inward currents, whereas mature myelin basic protein-expressing oligodendrocytes in cultures resistant to kainate toxicity showed no clear response to application of this agonist. We assayed expression of glutamate receptor subunits (GluR) -2, -4, -6, -7, and KA2 using immunoblot analysis and found that expression of all of these glutamate receptors was significantly down-regulated in mature oligodendrocytes. These results suggest a striking developmental regulation of glutamate receptors in oligodendrocytes and suggest that the vulnerability of oligodendrocytes to non- N-methyl-D-aspartate receptor-mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12503086     DOI: 10.1002/jnr.10472

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


  51 in total

1.  Role of metabotropic glutamate receptors in oligodendrocyte excitotoxicity and oxidative stress.

Authors:  Wenbin Deng; Hong Wang; Paul A Rosenberg; Joseph J Volpe; Frances E Jensen
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-10       Impact factor: 11.205

Review 2.  Axonal signals and oligodendrocyte differentiation.

Authors:  Maura Bozzali; Lawrence Wrabetz
Journal:  Neurochem Res       Date:  2004-05       Impact factor: 3.996

Review 3.  Reversal or reduction of glutamate and GABA transport in CNS pathology and therapy.

Authors:  Nicola J Allen; Ragnhildur Káradóttir; David Attwell
Journal:  Pflugers Arch       Date:  2004-08-24       Impact factor: 3.657

Review 4.  Pathophysiology of glia in perinatal white matter injury.

Authors:  Stephen A Back; Paul A Rosenberg
Journal:  Glia       Date:  2014-03-31       Impact factor: 7.452

5.  Cyclic GMP-dependent pathways protect differentiated oligodendrocytes from multiple types of injury.

Authors:  Joyce A Benjamins; Liljana Nedelkoska
Journal:  Neurochem Res       Date:  2006-12-27       Impact factor: 3.996

Review 6.  Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances.

Authors:  Joseph J Volpe
Journal:  Lancet Neurol       Date:  2009-01       Impact factor: 44.182

7.  Differential sensitivity of oligodendrocytes and motor neurons to reactive nitrogen species: implications for multiple sclerosis.

Authors:  Amy Bishop; Kimberly Green Hobbs; Asuka Eguchi; Stephanie Jeffrey; Lorraine Smallwood; Cedona Pennie; James Anderson; Alvaro G Estévez
Journal:  J Neurochem       Date:  2009-01-19       Impact factor: 5.372

8.  In utero PCP exposure alters oligodendrocyte differentiation and myelination in developing rat frontal cortex.

Authors:  Josette S Lindahl; Barton R Kjellsen; Jamie Tigert; Robin Miskimins
Journal:  Brain Res       Date:  2008-07-15       Impact factor: 3.252

9.  Axon-glia synapses are highly vulnerable to white matter injury in the developing brain.

Authors:  Yan Shen; Xiao-Bo Liu; David E Pleasure; Wenbin Deng
Journal:  J Neurosci Res       Date:  2011-08-02       Impact factor: 4.164

10.  BRAIN MYELINATION IN PREVALENT NEUROPSYCHIATRIC DEVELOPMENTAL DISORDERS: PRIMARY AND COMORBID ADDICTION.

Authors:  George Bartzokis
Journal:  Adolesc Psychiatry       Date:  2005
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.