Literature DB >> 8666670

Disrupted glial fibrillary acidic protein network in astrocytes from vimentin knockout mice.

M Galou1, E Colucci-Guyon, D Ensergueix, J L Ridet, M Gimenez y Ribotta, A Privat, C Babinet, P Dupouey.   

Abstract

Glial fibrillary acidic protein (GFAP) is an intermediate filament protein expressed predominantly in astrocytes. The study of its expression in the astrocyte lineage during development and in reactive astrocytes has revealed an intricate relationship with the expression of vimentin, another intermediate filament protein widely expressed in embryonic development. these findings suggested that vimentin could be implicated in the organization of the GFAP network. To address this question, we have examined GFAP expression and network formation in the recently generated vimentin knockout (Vim-) mice. We show that the GFAP network is disrupted in astrocytes that normally coexpress vimentin and GFAP, e.g., those of the corpus callosum or the Bergmann glia of cerebellum. Furthermore, Western blot analysis of GFAP protein content in the cerebellum suggests that posttranslational mechanisms are implicated in the disturbance of GFAP network formation. The role of vimentin in this process was further suggested by transfection of Vim-cultured astrocytes with a vimentin cDNA, which resulted in the normal assembly of the GFAP network. Finally, we examined GFAP expression after stab wound-induced astrogliosis. We demonstrate that in Vim- mice, reactive astrocytes that normally express both GFAP and vimentin do not exhibit GFAP immunoreactivity, whereas those that normally express GFAP only retain GFAP immunoreactivity. Taken together, these results show that in astrocytes, where vimentin is normally expressed with GFAP fails to assemble into a filamentous network in the absence of vimentin. In these cells, therefore, vimentin appears necessary to stabilize GFAP filaments and consequently the network formation.

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Year:  1996        PMID: 8666670      PMCID: PMC2120844          DOI: 10.1083/jcb.133.4.853

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  47 in total

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2.  Molecular interactions in intermediate-sized filaments revealed by chemical cross-linking. Heteropolymers of vimentin and glial filament protein in cultured human glioma cells.

Authors:  R A Quinlan; W W Franke
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3.  Localization of vimentin, the nonspecific intermediate filament protein, in embryonal glia and in early differentiating neurons. In vivo and in vitro immunofluorescence study of the rat embryo with vimentin and neurofilament antisera.

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4.  Immunohistochemical studies on the proliferation of reactive astrocytes and the expression of cytoskeletal proteins following brain injury in rats.

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5.  Site-specific phosphorylation induces disassembly of vimentin filaments in vitro.

Authors:  M Inagaki; Y Nishi; K Nishizawa; M Matsuyama; C Sato
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6.  Glial fibrillary acidic protein in the cytoskeletal and soluble protein fractions of the developing rat brain.

Authors:  G D Malloch; J B Clark; F R Burnet
Journal:  J Neurochem       Date:  1987-01       Impact factor: 5.372

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Authors:  S Fedoroff; R White; J Neal; L Subrahmanyan; V I Kalnins
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Journal:  J Cell Biol       Date:  1983-06       Impact factor: 10.539

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Authors:  J Frisén; C B Johansson; C Török; M Risling; U Lendahl
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6.  A novel and efficient gene transfer strategy reduces glial reactivity and improves neuronal survival and axonal growth in vitro.

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7.  Dynamics of the expression of intermediate filaments vimentin and desmin during myofibroblast differentiation after corneal injury.

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8.  The 14-3-3 protein epsilon isoform expressed in reactive astrocytes in demyelinating lesions of multiple sclerosis binds to vimentin and glial fibrillary acidic protein in cultured human astrocytes.

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