Expression of rat cGMP-binding cGMP-specific phosphodiesterase mRNA in Purkinje cell layers during postnatal neuronal development

被引:80
作者
Kotera, J [1 ]
Yanaka, N [1 ]
Fujishige, K [1 ]
Imai, Y [1 ]
Akatsuka, H [1 ]
Ishizuka, T [1 ]
Kawashima, K [1 ]
Omori, K [1 ]
机构
[1] TANABE SEIYAKU CO LTD,LEAD GENERAT RES LAB,YODOGAWA KU,OSAKA 532,JAPAN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 249卷 / 02期
关键词
rat; cGMP; phosphodiesterase; Purkinje cell layers; neuronal development;
D O I
10.1111/j.1432-1033.1997.t01-1-00434.x
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
The cDNA encoding rat cGMP-binding, cGMP-specific phosphodiesterase (cGB-PDE) was isolated from a rat lung cDNA library. Although the deduced amino acid sequence showed 93.4% similarity with that of bovine cGB-PDE, the N-terminal portion of rat cGB-PDE was extremely different from that of bovine. Northern blot analysis indicated that cGB-PDE transcripts in rats were expressed not only in aorta and lung, but also in several other tissues including cerebellum. fn situ hybridization analysis demonstrated that cerebellar expression of cGB-PDE was confined to Purkinje cell layers in adult rats. To clarify the role of cGB-PDE in the cerebellum, we investigated expression of cGB-PDE mRNA in rats of various apes. cGB-PDE mRNA was not observed in the cerebellum of newborn rats, but levels of a cGB-PDE mRNA were markedly increased between 4 days and 28 days of age and reached a maximum ill eight-week-old rats. In this study, we suggest that cGB-PDE plays important roles not only in regulating the relaxation of vascular vessels, but also in establishing neuronal networks in the cerebellum at an early postnatal stage. In addition the NO/cGMP/cGB-PDE pathway appears to be essential for the induction of long-term depression.
引用
收藏
页码:434 / 442
页数:9
相关论文
共 58 条
[1]  
AHN HS, 1989, BIOCHEM PHARMACOL, V38, P3331
[2]   IMMUNOHISTOCHEMICAL LOCALIZATION OF GUANYLATE-CYCLASE WITHIN NEURONS OF RAT-BRAIN [J].
ARIANO, MA ;
LEWICKI, JA ;
BRANDWEIN, HJ ;
MURAD, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (04) :1316-1320
[3]  
BEAVO JA, 1994, MOL PHARMACOL, V46, P399
[4]   INDUCIBLE CYTOSOLIC ENZYME-ACTIVITY FOR THE PRODUCTION OF NITROGEN-OXIDES FROM L-ARGININE IN HEPATOCYTES [J].
BILLIAR, TR ;
CURRAN, RD ;
STUEHR, DJ ;
STADLER, J ;
SIMMONS, RL ;
MURRAY, SA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (03) :1034-1040
[5]   DEVELOPMENTAL EXPRESSION OF CALMODULIN-DEPENDENT CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE IN RAT-BRAIN [J].
BILLINGSLEY, ML ;
POLLI, JW ;
BALABAN, CD ;
KINCAID, RL .
DEVELOPMENTAL BRAIN RESEARCH, 1990, 53 (02) :253-263
[6]   LOCALIZATION OF NITRIC-OXIDE SYNTHASE INDICATING A NEURAL ROLE FOR NITRIC-OXIDE [J].
BREDT, DS ;
HWANG, PM ;
SNYDER, SH .
NATURE, 1990, 347 (6295) :768-770
[7]   NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[8]   NITRIC-OXIDE SYNTHASE PROTEIN AND MESSENGER-RNA ARE DISCRETELY LOCALIZED IN NEURONAL POPULATIONS OF THE MAMMALIAN CNS TOGETHER WITH NADPH DIAPHORASE [J].
BREDT, DS ;
GLATT, CE ;
HWANG, PM ;
FOTUHI, M ;
DAWSON, TM ;
SNYDER, SH .
NEURON, 1991, 7 (04) :615-624
[9]   CLONED AND EXPRESSED NITRIC-OXIDE SYNTHASE STRUCTURALLY RESEMBLES CYTOCHROME-P-450 REDUCTASE [J].
BREDT, DS ;
HWANG, PM ;
GLATT, CE ;
LOWENSTEIN, C ;
REED, RR ;
SNYDER, SH .
NATURE, 1991, 351 (6329) :714-718
[10]   EXPRESSION OF SOLUBLE GUANYLYL CYCLASE GENE IN ADULT-RAT BRAIN [J].
BURGUNDER, JM ;
CHEUNG, PT .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (02) :211-217