Neuronal nitric oxide synthase alternatively spliced forms: Prominent functional localizations in the brain

被引:245
作者
Eliasson, MJL
Blackshaw, S
Schell, MJ
Snyder, SH
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PHARMACOL & MOL SCI,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT PSYCHIAT & BEHAV SCI,BALTIMORE,MD 21205
关键词
ornithine transcarbamoylase; postsynaptic density protein 95; citrulline;
D O I
10.1073/pnas.94.7.3396
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuronal nitric-oxide synthase (nNOS) is subject to alternative splicing, In mice with targeted deletions of exon 2 (nNOS(Delta/Delta)), two alternatively spliced forms, nNOS beta and gamma, which lack exon 2, have been described, We have compared localizations of native nNOS alpha and nNOS beta and gamma by in situ hybridization and immunohistochemistry in wild-type and nNOS(Delta/Delta) mice, To assess nNOS catalytic activity in intact animals we localized citrulline, which is formed stoichiometrically with NO, by immunohistochemistry. nNOS beta is prominent In several brain regions of wild-type animals and shows 2-to 3-fold up-regulation in the cortex and striatum of nNOS(Delta/Delta) animals, The persistence of much nNOS mRNA and protein, and distinct citrulline immunoreactivity (cit-IR) in the ventral cochlear nuclei and some cit-IR in the striatum and lateral tegmental nuclei, indicate that nNOS beta is a major functional form of the enzyme in these regions, Thus, nNOS beta, and possibly other uncharacterized splice forms, appear to be important physiological sources of NO in discrete brain regions and may account for the relatively modest level of impairment in nNOS(Delta/Delta) animals.
引用
收藏
页码:3396 / 3401
页数:6
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