INDUCTION AND VARIANTS OF NEURONAL NITRIC-OXIDE SYNTHASE TYPE-I DURING SYNAPTOGENESIS

被引:86
作者
OGILVIE, P
SCHILLING, K
BILLINGSLEY, ML
SCHMIDT, HHHW
机构
[1] UNIV WURZBURG,MED KLIN,D-97078 WURZBURG,GERMANY
[2] UNIV ULM,ANAT & ZELLBIOL ABT,D-89081 ULM,GERMANY
[3] PENN STATE UNIV,COLL MED,DEPT PHARMACOL,HERSHEY,PA 17033
[4] PENN STATE UNIV,COLL MED,CTR CELL & MOLEC BIOL,HERSHEY,PA 17033
关键词
EXPRESSION; DEVELOPMENT; NITRO-L-ARGININE; SYNAPTOGENESIS;
D O I
10.1096/fasebj.9.9.7541381
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
In the adult central nervous system, nitric oxide (NO) is formed from L-arginine by the so-called constitutive or type I NO synthase (NOS-I-155) However, expression of NOS-I-155 immunoreactivity and activity was low or not detectable in developing mouse and rat brain. NOS-I-155 was sharply induced coincident with the onset of synaptogenesis in specific brain regions, This was followed by a second phase in which total NOS-I-155 expression decreased both in specific cell populations and in the total synaptosomal subcellular fraction, Furthermore, two putative variants of NOS-I were transiently observed: an NOS-I-immunoreactive protein with increased electrophoretic mobility (NOS-I-144) and a transient hypersensitivity of NOS-I-155 to the competitive substrate inhibitor N-omega-nitro-L-arginine. It is concluded that NOS-I expression is not constitutive but locally induced. In the central nervous system, this regionally specific, biphasic pattern of postnatal NOS-I induction is consistent with a role for NO in synaptogenesis and synaptic plasticity.
引用
收藏
页码:799 / 806
页数:8
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