Literature DB >> 9417833

Axonal and nonneuronal cell responses to spinal cord injury in mice lacking glial fibrillary acidic protein.

X Wang1, A Messing, S David.   

Abstract

We have examined the regeneration of corticospinal tract fibers and expression of various extracellular matrix (ECM) molecules and intermediate filaments [vimentin and glial fibrillary acidic protein (GFAP)] after dorsal hemisection of the spinal cord of adult GFAP-null and wild-type littermate control mice. The expression of these molecules was also examined in the uninjured spinal cord. There was no increase in axon sprouting or long distance regeneration in GFAP-/- mice compared to the wild type. In the uninjured spinal cord (i) GFAP was expressed in the wild type but not the mutant mice, while vimentin was expressed in astrocytes in the white matter of both types of mice; (ii) laminin and fibronectin immunoreactivity was localized to blood vessels and meninges; (iii) tenascin and chondroitin sulfate proteoglycan (CSPG) labeling was detected in astrocytes and the nodes of Ranvier in the white matter; and (iv) in addition, CSPG labeling which was generally less intense in the gray matter of mutant mice. Ten days after hemisection there was a large increase in vimentin+ cells at the lesion site in both groups of mice. These include astrocytes as well as meningeal cells that migrate into the wound. The center of these lesions was filled by laminin+/fibronectin+ cells. Discrete strands of tenascin-like immunoreactivity were seen in the core of the lesion and lining its walls. Marked increases in CSPG labeling was observed in the CNS parenchyma on either side of the lesion. These results indicate that the absence of GFAP in reactive astrocytes does not alter axonal sprouting or regeneration. In addition, except for CSPG, the expression of various ECM molecules appears unaltered in GFAP-/- mice. Copyright 1997 Academic Press.

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Year:  1997        PMID: 9417833     DOI: 10.1006/exnr.1997.6702

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


  14 in total

1.  Role of chondroitin sulfate proteoglycans in axonal conduction in Mammalian spinal cord.

Authors:  Arsen S Hunanyan; Guillermo García-Alías; Valentina Alessi; Joel M Levine; James W Fawcett; Lorne M Mendell; Victor L Arvanian
Journal:  J Neurosci       Date:  2010-06-09       Impact factor: 6.167

2.  Increased adenine nucleotide translocator 1 in reactive astrocytes facilitates glutamate transport.

Authors:  Charles R Buck; Michael J Jurynec; Deepak K Gupta; Alick K T Law; Johannes Bilger; Douglas C Wallace; Robert J McKeon
Journal:  Exp Neurol       Date:  2003-06       Impact factor: 5.330

3.  Axonal plasticity and functional recovery after spinal cord injury in mice deficient in both glial fibrillary acidic protein and vimentin genes.

Authors:  V Menet; M Prieto; A Privat; M Giménez y Ribotta
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-14       Impact factor: 11.205

4.  EphA4 deficient mice maintain astroglial-fibrotic scar formation after spinal cord injury.

Authors:  Julia E Herrmann; Ravi R Shah; Andrea F Chan; Binhai Zheng
Journal:  Exp Neurol       Date:  2010-02-17       Impact factor: 5.330

Review 5.  Glial fibrillary acidic protein: from intermediate filament assembly and gliosis to neurobiomarker.

Authors:  Zhihui Yang; Kevin K W Wang
Journal:  Trends Neurosci       Date:  2015-05-11       Impact factor: 13.837

Review 6.  Role of GFAP in CNS injuries.

Authors:  Michael Brenner
Journal:  Neurosci Lett       Date:  2014-02-06       Impact factor: 3.046

Review 7.  Dual roles of astrocytes in plasticity and reconstruction after traumatic brain injury.

Authors:  Yunxiang Zhou; Anwen Shao; Yihan Yao; Sheng Tu; Yongchuan Deng; Jianmin Zhang
Journal:  Cell Commun Signal       Date:  2020-04-15       Impact factor: 5.712

8.  Adult NG2+ cells are permissive to neurite outgrowth and stabilize sensory axons during macrophage-induced axonal dieback after spinal cord injury.

Authors:  Sarah A Busch; Kevin P Horn; Fernando X Cuascut; Alicia L Hawthorne; Lianhua Bai; Robert H Miller; Jerry Silver
Journal:  J Neurosci       Date:  2010-01-06       Impact factor: 6.167

Review 9.  Axon regeneration after spinal cord injury: insight from genetically modified mouse models.

Authors:  Jae K Lee; Binhai Zheng
Journal:  Restor Neurol Neurosci       Date:  2008       Impact factor: 2.406

10.  Müller glia reactivity follows retinal injury despite the absence of the glial fibrillary acidic protein gene in Xenopus.

Authors:  Reyna I Martinez-De Luna; Ray Y Ku; Alexandria M Aruck; Francesca Santiago; Andrea S Viczian; Diego San Mauro; Michael E Zuber
Journal:  Dev Biol       Date:  2016-03-18       Impact factor: 3.582

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