Acidic pH rapidly increases immunoreactivity of glial fibrillary acidic protein in cultured astrocytes

Glia ◽  
1995 ◽  
Vol 13 (4) ◽  
pp. 319-322 ◽  
Author(s):  
Tae H. Oh ◽  
George J. Markelonis ◽  
Jon R. Von Visger ◽  
Bonsook Baik ◽  
Michael T. Shipley
1996 ◽  
Vol 133 (4) ◽  
pp. 853-863 ◽  
Author(s):  
M Galou ◽  
E Colucci-Guyon ◽  
D Ensergueix ◽  
J L Ridet ◽  
M Gimenez y Ribotta ◽  
...  

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.


1995 ◽  
Vol 200 (3) ◽  
pp. 175-178 ◽  
Author(s):  
Rubén F. Iacono ◽  
Analia Nessi de Aviñón ◽  
Francisco A. Rosetti ◽  
María I. Berría

1996 ◽  
Vol 2 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Mikio Ishikawa ◽  
Tetsuro Tsukamoto ◽  
Teiji Yamamoto

The chronic demyelinated plaque of multiple sclerosis (MS) is characterised by a loss of oligodendrocytes, astrogliosis, and incomplete or no remyelination which probably results in part from the suppressive effects of gliotic astrocytes on myelin formation. We explanted mouse cerebella on astrocyte cultures which had been maintained for 2 to 12 weeks and assessed the myelination in the cerebellar tissue at 18 days after explanation. Myelination occurred vigorously in the tissue explanted on 2-to 4-week-old astrocytes, but was poorer in the tissue explanted on astrocytes older than 4 weeks. No myelin sheath was formed on 12-week-old astrocytes, although axons developed equally as well as those in the tissues explanted on 2-week-old astrocytes. As astrocytes were maintained longer, they became fibrous and immunostained more deeply with anti-glial fibrillary acidic protein antibody, being analogous to astrogliosis. These findings imply that astrogliosis in chronic demyelinated lesions of MS may potentially block remyelination.


1990 ◽  
Vol 49 (4) ◽  
pp. 399-405 ◽  
Author(s):  
Michael D. Norenberg ◽  
Joseph T. Neary ◽  
Luz-Oliva B. Norenberg ◽  
Michelin McCarthy

Pathology ◽  
1983 ◽  
Vol 15 (4) ◽  
pp. 373-378 ◽  
Author(s):  
Stephen J. Lolait ◽  
J.H. Harmer ◽  
G. Auteri ◽  
J.S. Pedersen ◽  
B.H. Toh

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