ANALYSIS OF GLIAL FIBRILLARY ACIDIC PROTEIN, NEUROFILAMENT PROTEIN, ACTIN AND HEAT-SHOCK PROTEINS IN HUMAN FETAL BRAIN DURING THE 2ND TRIMESTER

Citation
Da. Aquino et al., ANALYSIS OF GLIAL FIBRILLARY ACIDIC PROTEIN, NEUROFILAMENT PROTEIN, ACTIN AND HEAT-SHOCK PROTEINS IN HUMAN FETAL BRAIN DURING THE 2ND TRIMESTER, Developmental brain research, 91(1), 1996, pp. 1-10
Citations number
40
Categorie Soggetti
Neurosciences
ISSN journal
01653806
Volume
91
Issue
1
Year of publication
1996
Pages
1 - 10
Database
ISI
SICI code
0165-3806(1996)91:1<1:AOGFAP>2.0.ZU;2-1
Abstract
Glial fibrillary acidic protein (GFAP), the 66 kDa neurofilament prote in (NF-66), actin, the 27 kDa heat shock protein (HSP27) and the 70 kD a constitutive heat shock protein (HSC70) were analyzed in human fetal brain during the second trimester, from 10 to 24 gestational weeks (G W). By immunohistochemistry, cell-type specific localization of GFAP a nd NF-66 in astrocytes and neurons, respectively, was confirmed. HSP27 was expressed mostly in the nuclear region of neurons and non-neurona l cells, and HSC70 was widely distributed throughout the tissue. By qu antitative immunoblotting, GFAP was not detectable in gray matter of p refrontal cortex prior to 16 GW. Between 16 and 21 GW, the content of GFAP rose slowly. Thereafter, GFAP accumulated rapidly. The content of GFAP in different brain regions (prefrontal, parietal, and occipital cortices) differed significantly at 22 GW. In contrast, NF-66 was alre ady highly expressed at 10 GW, slowly rose to maximal values by 18 GW, and thereafter remained stationary. In contrast to GFAP, the content of NF-66 was similar in different brain regions at 22 GW. Although act in was abundant throughout the second trimester, a sharp drop in its c ontent in the prefrontal cortex was detected at 17 GW. To explain such a decrease, two heat shock proteins were analyzed. HSP27, known to mo dulate actin polymerization, was found to increase sharply at 16-17 GW . In contrast, HSC70 remained constant during the second trimester and was highly expressed in the fetal brain, at a level comparable to tha t in the adult brain.