GLIAL FIBRILLARY ACIDIC PROTEIN MESSENGER-RNA ISOTYPES - EXPRESSION IN-VITRO AND IN-VIVO

Citation
E. Galea et al., GLIAL FIBRILLARY ACIDIC PROTEIN MESSENGER-RNA ISOTYPES - EXPRESSION IN-VITRO AND IN-VIVO, Journal of neuroscience research, 41(4), 1995, pp. 452-461
Citations number
39
Categorie Soggetti
Neurosciences
ISSN journal
03604012
Volume
41
Issue
4
Year of publication
1995
Pages
452 - 461
Database
ISI
SICI code
0360-4012(1995)41:4<452:GFAPMI>2.0.ZU;2-H
Abstract
Glial fibrillary acidic protein (GFAP) and its mRNA, primarily express ed in astrocytes, are also expressed in peripheral nervous system Schw ann cells as well as in certain non-neural tissues, Schwann cells expr ess a GFAP mRNA (GFAP-beta) which differs from the CNS-type mRNA (GFAP -alpha) by the presence of an extended 5' untranslated region, We have developed a polymerase chain reaction assay which allows distinction of these two GFAP mRNAs, as well as quantitative analysis of their lev els, In the cultured rat Schwannoma cell line RT4-D6, GFAP-beta was th e major GFAP mRNA species, accounting for at least 75% of total GFAP ( alpha + beta) mRNA, GFAP-beta was also detected in primary rat astrocy te cultures, where it constituted approximately 5% of the total GFAP m RNA, as well as in RNA samples prepared from normal rat cerebral corte x, and from hamster and human brain, In rat cortex, the temporal expre ssion of GFAP-beta mRNA paralleled that of total GFAP mRNA, with plate au levels reached between postnatal days 15 and 20. In astrocyte cultu res, the relative levels of GFAP-alpha and -beta mRNAs were differenti ally regulated by exposure to interferorm-gamma (10 to 25 units/ml), w hich caused an increase in GFAP-beta levels while at the same time no change or a small decrease in total GFAP levels. In rat brain cortical slices, 4 hr exposure to 25 units/ml interferon-gamma decreased total GFAP mRNA levels over tenfold, while GFAP-beta levels were unaffected . These data indicate that a second form of the GFAP mRNA is expressed in astrocytes both in vivo and in vitro and provide evidence for inde pendent regulation of these two GFAP mRNA species. (C) 1995 Wiley-Liss , Inc.