Literature DB >> 10833310

Reactions of oligodendrocytes to spinal cord injury: cell survival and myelin repair.

E Frei1, I Klusman, L Schnell, M E Schwab.   

Abstract

The aim of this study was to elucidate whether oligodendrocytes die in fiber tracts that are spared by a spinal cord injury but are in close vicinity of inflammatory cells. Adult rat spinal cords were studied histologically 1 day to 2 weeks after a contusion lesion that left the ventral white matter largely intact. Massive oligodendrocyte death occurred in the lesion center, along with the death of neurons, microglia, and astrocytes. Oligodendrocytes, specifically positive for proteolipid protein (PLP) mRNA, were counted in the ventral white matter where axons at the rostral and caudal edges of the lesion were histologically intact. Although these regions contained many macrophages and neutrophils hypothesized to contribute to secondary tissue loss, there was no significant loss of oligodendrocytes. In the ventral funiculus, 3 and 6 mm rostral and caudal to the lesion, oligodendrocyte numbers were also unchanged, in spite of the presence of many activated microglial cells. From day 7 on, oligodendrocytes in close vicinity to the lesion increased their expression of PLP mRNA. We conclude that, at least within the first 2 weeks after a spinal cord contusion lesion, there is no major devastating influence of inflammatory cells or their mediators on oligodendrocytes. When death occurs, it may be due to mechanical trauma, ischemia, or excitotoxicity within the lesion or it may occur as a result of axonal degeneration. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10833310     DOI: 10.1006/exnr.2000.7379

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  11 in total

1.  Protective effect of a new hypothalamic peptide against cobra venom and trauma-induced neuronal injury.

Authors:  A A Galoyan; J S Sarkissian; T K Kipriyan; E J Sarkissian; E A Chavushyan; R M Sulkhanyan; I B Meliksetyan; S S Abrahamyan; Z A Avetisyan; N A Otieva
Journal:  Neurochem Res       Date:  2001-09       Impact factor: 3.996

2.  Proliferation of NG2-positive cells and altered oligodendrocyte numbers in the contused rat spinal cord.

Authors:  D M McTigue; P Wei; B T Stokes
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

3.  Reversible demyelination, blood-brain barrier breakdown, and pronounced neutrophil recruitment induced by chronic IL-1 expression in the brain.

Authors:  Carina C Ferrari; Amaicha M Depino; Federico Prada; Nara Muraro; Sandra Campbell; Osvaldo Podhajcer; V Hugh Perry; Daniel C Anthony; Fernando J Pitossi
Journal:  Am J Pathol       Date:  2004-11       Impact factor: 4.307

4.  Effects of axon degeneration on oligodendrocyte lineage cells: dorsal rhizotomy evokes a repair response while axon degeneration rostral to spinal contusion induces both repair and apoptosis.

Authors:  Fang Sun; Chien-Liang Glenn Lin; Dana McTigue; Xiu Shan; C Amy Tovar; Jacqueline C Bresnahan; Michael S Beattie
Journal:  Glia       Date:  2010-08-15       Impact factor: 7.452

5.  Intermittent noxious stimulation following spinal cord contusion injury impairs locomotor recovery and reduces spinal brain-derived neurotrophic factor-tropomyosin-receptor kinase signaling in adult rats.

Authors:  S M Garraway; J D Turtle; J R Huie; K H Lee; M A Hook; S A Woller; J W Grau
Journal:  Neuroscience       Date:  2011-10-18       Impact factor: 3.590

6.  Patterns of Nogo mRNA and protein expression in the developing and adult rat and after CNS lesions.

Authors:  Andrea B Huber; Oliver Weinmann; Christian Brösamle; Thomas Oertle; Martin E Schwab
Journal:  J Neurosci       Date:  2002-05-01       Impact factor: 6.167

7.  Dorsal column sensory axons degenerate due to impaired microvascular perfusion after spinal cord injury in rats.

Authors:  Johongir M Muradov; Eric E Ewan; Theo Hagg
Journal:  Exp Neurol       Date:  2013-08-23       Impact factor: 5.330

8.  Regulatory effects of intermittent noxious stimulation on spinal cord injury-sensitive microRNAs and their presumptive targets following spinal cord contusion.

Authors:  Eric R Strickland; Sarah A Woller; Sandra M Garraway; Michelle A Hook; James W Grau; Rajesh C Miranda
Journal:  Front Neural Circuits       Date:  2014-09-18       Impact factor: 3.492

9.  Early proliferation does not prevent the loss of oligodendrocyte progenitor cells during the chronic phase of secondary degeneration in a CNS white matter tract.

Authors:  Sophie C Payne; Carole A Bartlett; Donna L Savigni; Alan R Harvey; Sarah A Dunlop; Melinda Fitzgerald
Journal:  PLoS One       Date:  2013-06-11       Impact factor: 3.240

Review 10.  Stem cell therapy for central nerve system injuries: glial cells hold the key.

Authors:  Li Xiao; Chikako Saiki; Ryoji Ide
Journal:  Neural Regen Res       Date:  2014-07-01       Impact factor: 5.135

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