SYNAPTIC RELATIONSHIP BETWEEN SUBSTANCE-P AND THE SUBSTANCE-P RECEPTOR - LIGHT AND ELECTRON-MICROSCOPIC CHARACTERIZATION OF THE MISMATCH BETWEEN NEUROPEPTIDES AND THEIR RECEPTORS

被引:262
作者
LIU, HT
BROWN, JL
JASMIN, L
MAGGIO, JE
VIGNA, SR
MANTYH, PW
BASBAUM, AI
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PHYSIOL,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,KECK CTR INTEGRAT NEUROSCI,SAN FRANCISCO,CA 94143
[3] HARVARD UNIV,SCH MED,DEPT BIOL CHEM & MOLEC PHARMACOL,BOSTON,MA 02115
[4] DUKE UNIV,MED CTR,DEPT CELL BIOL,DURHAM,NC 27710
[5] VET ADM MED CTR,MOLEC NEUROBIOL LAB,MINNEAPOLIS,MN 55417
关键词
D O I
10.1073/pnas.91.3.1009
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
Light microscopic studies have demonstrated significant mismatches in the location of neuropeptides and their respective binding sites in the central nervous system. In the present study we used an antiserum raised against a synthetic peptide corresponding to the carboxyl-terminal tail of the substance P (SP) receptor (SPR) to further explore the relationship between a neuropeptide and its receptor. Light microscopy revealed an excellent correlation between the patterns of SPR immunoreactivity and of I-125-labeled SPR-binding sites in the central nervous system. The SPR appeared to be exclusively expressed by neurons; in fact, the SPR decorates the somatic and dendritic surface of neurons, producing Golgi-like images. Electron microscopic analysis in cortex, striatum, and spinal cord revealed that approximately 70% of the surface membrane of immunoreactive neurons is SPR laden. Simultaneous electron microscopic labeling of SP and SPR demonstrated significant mismatch at the synaptic level. Although some SP terminals contacted SPR-immunoreactive membrane, no more than 15% of the SPR-laden membrane apposed synaptic terminals. These results suggest that in contrast to more ''classical'' central and peripheral nervous system synapses, wherein the receptor immediately apposes the site of neurotransmitter storage and release, much of the surface of SPR-expressing neurons can be targeted by SP that diffuses a considerable distance from its site of release.
引用
收藏
页码:1009 / 1013
页数:5
相关论文
共 41 条
[1]   GABAERGIC TERMINALS ARE PRESYNAPTIC TO PRIMARY AFFERENT TERMINALS IN SUBSTANTIA GELATINOSA OF RAT SPINAL-CORD [J].
BARBER, RP ;
VAUGHN, JE ;
SAITO, K ;
MCLAUGHLIN, BJ ;
ROBERTS, E .
BRAIN RESEARCH, 1978, 141 (01) :35-55
[2]   MONO-AMINE INNERVATION OF RAT CEREBRAL-CORTEX - SYNAPTIC AND NON-SYNAPTIC AXON TERMINALS [J].
BEAUDET, A ;
DESCARRIES, L .
NEUROSCIENCE, 1978, 3 (10) :851-+
[3]  
BEAUDET A, 1985, ANN NY ACAD SCI, V668, P173
[4]   ULTRASTRUCTURAL DEMONSTRATION OF NONSYNAPTIC RELEASE SITES IN THE CENTRAL-NERVOUS-SYSTEM OF THE SNAIL LYMNAEA-STAGNALIS, THE INSECT PERIPLANETA-AMERICANA, AND THE RAT [J].
BUMA, P ;
ROUBOS, EW .
NEUROSCIENCE, 1986, 17 (03) :867-879
[5]   SPINAL NEURONS EXHIBITING A SPECIFIC NOCICEPTIVE RESPONSE RECEIVE ABUNDANT SUBSTANCE-P-CONTAINING SYNAPTIC CONTACTS [J].
DE KONINCK, Y ;
RIBEIRODASILVA, A ;
HENRY, JL ;
CUELLO, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (11) :5073-5077
[6]  
DEBIASI S, 1988, P NATL ACAD SCI USA, V85, P7820
[7]   EFFECT OF PEPTIDASE INHIBITION ON THE PATTERN OF INTRASPINALLY RELEASED IMMUNOREACTIVE SUBSTANCE-P DETECTED WITH ANTIBODY MICROPROBES [J].
DUGGAN, AW ;
SCHAIBLE, HG ;
HOPE, PJ ;
LANG, CW .
BRAIN RESEARCH, 1992, 579 (02) :261-269
[8]   RELEASE, SPREAD AND PERSISTENCE OF IMMUNOREACTIVE NEUROKININ A IN THE DORSAL HORN OF THE CAT FOLLOWING NOXIOUS CUTANEOUS STIMULATION - STUDIES WITH ANTIBODY MICROPROBES [J].
DUGGAN, AW ;
HOPE, PJ ;
JARROTT, B ;
SCHAIBLE, HG ;
FLEETWOODWALKER, SM .
NEUROSCIENCE, 1990, 35 (01) :195-202
[9]   SELECTIVE ASSOCIATION OF N-METHYL ASPARTATE AND QUISQUALATE TYPES OF L-GLUTAMATE RECEPTOR WITH BRAIN POSTSYNAPTIC DENSITIES [J].
FAGG, GE ;
MATUS, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (21) :6876-6880
[10]  
FERTUCK H C, 1974, Proceedings of the National Academy of Sciences of the United States of America, V71, P1376, DOI 10.1073/pnas.71.4.1376