ONTOGENY OF PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE (PACAP) RECEPTORS IN THE RAT CEREBELLUM - A QUANTITATIVE AUTORADIOGRAPHIC STUDY

被引:58
作者
BASILLE, M
GONZALEZ, BJ
FOURNIER, A
VAUDRY, H
机构
[1] UNIV ROUEN,FAC SCI,INST FED RECH MULTIDISCIPLINAIRES PEPTIDES,INSERM,U413,F-76821 MONT ST AIGNAN,FRANCE
[2] UNIV QUEBEC,INST NATL RECH SCI SANTE,POINTE CLAIRE H9R 1G6,PQ,CANADA
来源
DEVELOPMENTAL BRAIN RESEARCH | 1994年 / 82卷 / 1-2期
关键词
PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE; PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE RECEPTOR; CEREBELLUM; ONTOGENY; EXTERNAL GRANULE CELL LAYER; INTERNAL GRANULE CELL LAYER; MEDULLA; QUANTITATIVE AUTORADIOGRAPHY;
D O I
10.1016/0165-3806(94)90150-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pituitary adenylate cyclase-activating polypeptide and PACAP receptors are both present in the rat cerebellar cortex, suggesting that PACAP may play an important role in the cerebellum. In the present study, the variation of the concentration of PACAP binding sites in the rat cerebellum was investigated during postnatal development by means of quantitative autoradiography, using [I-125]PACAP27 as a radioligand. In the external granule cell layer and the medulla, the density of PACAP binding sites was high at birth, markedly decreased from postnatal day 8 (P8) to P25 and finally vanished at the end of the third postnatal week. In the internal granule cell layer and molecular layer, PACAP binding sites were first detected at P8. In the internal granule cell layer, the density of binding sites slightly decreased during development but remained elevated in adults. Conversely, in the molecular layer, PACAP binding sites rapidly decreased during the second and third postnatal weeks and virtually disappeared after P25. In all four layers of the cerebellar cortex, the autoradiographic labeling was displaced by PACAP27 (IC50 close to 10(-8) M), but was not affected by VIP. No significant changes in IC50 and Hill coefficient were noticed in the various layers throughout development. The present study shows that all four layers of the cerebellar cortex express PACAP binding sites during development. The evolution of the receptor concentration exhibited differential profiles in the various layers but the specificity characteristics of the recognition sites were identical in all four structures. The intense and transient expression of PACAP binding sites in the external granule cell layer, a germinative matrix which generates the majority of cerebellar interneurons, supports the concept that PACAP may play important functions during histogenesis of the cerebellum.
引用
收藏
页码:81 / 89
页数:9
相关论文
共 40 条
[2]   TISSUE DISTRIBUTION OF PACAP AS DETERMINED BY RIA - HIGHLY ABUNDANT IN THE RAT-BRAIN AND TESTES [J].
ARIMURA, A ;
SOMOGYVARIVIGH, A ;
MIYATA, A ;
MIZUNO, K ;
COY, DH ;
KITADA, C .
ENDOCRINOLOGY, 1991, 129 (05) :2787-2789
[3]   RECEPTORS FOR PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE - COMPARISON WITH VASOACTIVE-INTESTINAL-PEPTIDE RECEPTORS [J].
ARIMURA, A .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1992, 3 (08) :288-294
[4]  
ARIMURA A, 1992, REGUL PEPTIDES, V37, P287
[5]  
ARIMURA A, 1993, 75TH END SOC ANN M
[6]   LOCALIZATION AND CHARACTERIZATION OF PACAP RECEPTORS IN THE RAT CEREBELLUM DURING DEVELOPMENT - EVIDENCE FOR A STIMULATORY EFFECT OF PACAP ON IMMATURE CEREBELLAR GRANULE CELLS [J].
BASILLE, M ;
GONZALEZ, BJ ;
LEROUX, P ;
JEANDEL, L ;
FOURNIER, A ;
VAUDRY, H .
NEUROSCIENCE, 1993, 57 (02) :329-338
[7]   NEUROTROPHIC ACTION OF VIP ON SPINAL-CORD CULTURES [J].
BRENNEMAN, DE ;
EIDEN, LE ;
SIEGEL, RE .
PEPTIDES, 1985, 6 :35-39
[8]   STIMULATION OF RAT PANCREATIC TUMORAL AR4-2J CELL-PROLIFERATION BY PITUITARY ADENYLATE CYCLASE-ACTIVATING PEPTIDE [J].
BUSCAIL, L ;
CAMBILLAU, C ;
SEVA, C ;
SCEMAMA, JL ;
DENEEF, P ;
ROBBERECHT, P ;
CHRISTOPHE, J ;
SUSINI, C ;
VAYSSE, N .
GASTROENTEROLOGY, 1992, 103 (03) :1002-1008
[9]   PROPERTIES AND DISTRIBUTION OF RECEPTORS FOR PITUITARY ADENYLATE-CYCLASE ACTIVATING PEPTIDE (PACAP) IN RAT-BRAIN AND SPINAL-CORD [J].
CAUVIN, A ;
ROBBERECHT, P ;
DENEEF, P ;
GOURLET, P ;
VANDERMEERS, A ;
VANDERMEERSPIRET, MC ;
CHRISTOPHE, J .
REGULATORY PEPTIDES, 1991, 35 (02) :161-173
[10]  
DEUTSCH PJ, 1992, J BIOL CHEM, V267, P5108