Opposing changes of trimeric G protein levels during ontogenetic development of rat brain
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
11850064
DOI
10.1016/s0165-3806(01)00322-4
PII: S0165380601003224
Knihovny.cz E-zdroje
- MeSH
- buněčná diferenciace fyziologie MeSH
- down regulace fyziologie MeSH
- heterotrimerní G-proteiny metabolismus MeSH
- krysa rodu Rattus MeSH
- mozek růst a vývoj metabolismus MeSH
- neuroglie metabolismus MeSH
- neurony metabolismus MeSH
- novorozená zvířata MeSH
- potkani Wistar MeSH
- proteiny vázající GTP - alfa-podjednotka Gi2 MeSH
- proteiny vázající GTP - alfa-podjednotky Gi-Go metabolismus MeSH
- proteiny vázající GTP - alfa-podjednotky Gq-G11 MeSH
- proteiny vázající GTP - alfa-podjednotky Gs metabolismus MeSH
- proteiny vázající GTP - alfa-podjednotky MeSH
- proteiny vázající GTP metabolismus MeSH
- protoonkogenní proteiny metabolismus MeSH
- stárnutí metabolismus MeSH
- up regulace fyziologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- Gnai2 protein, rat MeSH Prohlížeč
- heterotrimerní G-proteiny MeSH
- olfactory G protein subunit alpha olf MeSH Prohlížeč
- proteiny vázající GTP - alfa-podjednotka Gi2 MeSH
- proteiny vázající GTP - alfa-podjednotky Gi-Go MeSH
- proteiny vázající GTP - alfa-podjednotky Gq-G11 MeSH
- proteiny vázající GTP - alfa-podjednotky Gs MeSH
- proteiny vázající GTP - alfa-podjednotky MeSH
- proteiny vázající GTP MeSH
- protoonkogenní proteiny MeSH
Developmental changes in the distribution of guanine nucleotide-binding regulatory proteins (G proteins) were investigated in the rat brain during postnatal development. Using a standard or high-resolution urea-SDS-PAGE and specific polyclonal antipeptide antibodies oriented against G(i)alpha1/G(i)alpha2, G(i)alpha3, G(s)alpha, G(o)alpha1/G(o)alpha2, G(q)alpha/G(11)alpha and Gbeta subunit, all these proteins were determined by quantitative immunoblotting in homogenates prepared from cortex, thalamus, hippocampus and pituitary of 1-, 7-, 12-, 18-, 25- and 90-day-old animals. The levels of the majority of G protein alpha subunits, namely G(i)alpha1, G(i)alpha2, G(i)alpha3, G(o)alpha1, G(o)alpha2, G(q)alpha, G(11)alpha and Gbeta, were high already at birth. Whereas the short variant of G(s)alpha, G(s)alphaS, rose sharply in all tested brain regions between postnatal day (PD) 1 and 90, the long variant of G(s)alpha, G(s)alphaL, was unchanged in cortex and thalamus and slightly increased in hippocampus. An increase was observed also in expression of G(i)alpha1/G(i)alpha2 and G(o)alpha1 protein, while G(o)alpha2 remained constant. Minority protein G(o)alpha* dramatically increased in cortex and thalamus, was unchanged in hippocampus and not detectable in pituitary. By contrast, the highest levels of G(i)alpha3 and G(q)alpha/G(11)alpha were detected as early as at PD 1. During the next 90 days, the immunological signal of G(i)alpha3 almost disappeared and G(q)alpha/G(11)alpha continuously declined to the levels corresponding to 50% of the levels determined at birth. Expression of Gbeta subunit was basically unchanged during postnatal development. Our present analysis indicates that G(s)alpha, G(i)alpha/G(o)alpha and G(q)alpha/G(11)alpha proteins are differently expressed in the course of brain development. Differential expression of the individual alpha subunits of trimeric G proteins during postnatal development suggests their different roles in maturation of the brain tissue.
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