glutamate;
group III mGluR;
mGluR4;
mGluR8;
osteoblasts;
RT-PCR;
cAMP accumulation;
NR1;
NR2D;
D O I:
10.1006/bbrc.2001.4355
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Reverse transcription polymerase chain reaction revealed expression of mRNAs for particular receptors for the central neurotransmitter L-glutamic acid (Glu) in primary cultures of rat calvarial osteoblastic cells under premature to mature states according to the duration of days in vitro, These included metabotropic Glu receptors (mGluR) such as mGluR4 and mGluR8, in addition to several ionotropic Glu receptor subunits including NR1 and NR2D. Expression of mRNAs was not detected with other mGluR and NR2A-C subunits irrespective of the maturity of cultured cells. The agonist for group III mGluR L-(+)-2-amino-4-phosphonobutyric acid significantly inhibited the forskolin-induced accumulation of cAMP in premature osteoblasts, which occurred in a manner sensitive to prevention by the group III mGluR antagonist (RS)alpha -cyclopropyl-4-phosphonophenylglycine. These results suggest that Glu may at least in part play a role in mechanisms associated with cellular proliferation and/or differentiation through group III mGluR functionally expressed in rat calvarial osteoblastic cells. (C) 2001 Academic Press.
机构:
GlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, ItalyGlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, Italy
Faedo, S.
Remelli, R.
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GlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, ItalyGlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, Italy
Remelli, R.
Corsi, M.
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GlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, ItalyGlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, Italy
Corsi, M.
Cavanni, P.
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GlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, ItalyGlaxoWellcome SpA, Med Res Ctr, GlaxoSmithKline Grp, I-37134 Verona, Italy
机构:
Univ Paris 05, CNRS, UMR8601, Paris 06, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Acher, F. C.
Courtiol, T.
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Univ Paris 05, CNRS, UMR8601, Paris 06, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Courtiol, T.
Brabet, I.
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机构:
Univ Montpellier 1, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, France
Univ Montpellier 2, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Brabet, I.
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机构:
Selvam, C.
Oueslati, N.
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Univ Montpellier 1, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, France
Univ Montpellier 2, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Oueslati, N.
Rigault, D.
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Univ Paris 05, CNRS, UMR8601, Paris 06, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Rigault, D.
Lemasson, I. A.
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Univ Paris 05, CNRS, UMR8601, Paris 06, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Lemasson, I. A.
Cesarini, S.
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Univ Paris 05, CNRS, UMR8601, Paris 06, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Cesarini, S.
Bertrand, H-O
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Parc Club Orsay Univ, F-91893 Orsay, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Bertrand, H-O
Goudet, C.
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Univ Montpellier 1, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, France
Univ Montpellier 2, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France
Goudet, C.
Pin, J. -P.
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Univ Montpellier 1, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, France
Univ Montpellier 2, Inst Genom Fonct, CNRS, UMR5203,INSERM,U661, F-34094 Montpellier, FranceUniv Paris 05, CNRS, UMR8601, Paris 06, France