Synaptic precedence during synapse formation between reciprocally connected neurons involves transmitter-receptor interactions and AA metabolites

被引:10
作者
Lovell, P
McMahon, B
Syed, NI
机构
[1] Univ Calgary, Fac Med, Dept Cell Biol & Anat, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Fac Med, Dept Biol Sci, Resp Res Grp, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Fac Med, Dept Biol Sci, Neurosci Res Grp, Calgary, AB T2N 4N1, Canada
关键词
D O I
10.1152/jn.2002.88.3.1328
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The cellular mechanisms that determine specificity of synaptic connections between mutually connected neurons in the nervous system have not yet been fully examined in vertebrate and invertebrate species. Here we report on a novel form of synaptic interaction during early stages of synapse formation between reciprocally connected Lymnaea neurons. Specifically, using soma-soma synapses between an identified dopaminergic neuron (also known as the giant dopamine cell), right pedal dorsal 1 (RPeD1), and a FMRFamidergic neuron, visceral dorsal 4 (VD4), we demonstrate that although reciprocal inhibitory synapses re-form between the somata after 24-36 h of pairing, VD4 is, however, the first cell to establish synaptic contacts with RPeD1 (within 12-18 h). We show that VD4 "captures" RPeD1 first as a postsynaptic cell by suppressing its transmitter secretory machinery during early stages of cell-cell pairing. The VD4-induced suppression of transmitter release from RPeD1 was transient, and it required transcription and de novo protein synthesis dependent step in VD4 but not in RPeD1. The VD4-induced effects on RPeD1 were mimicked by a FMRFamidelike peptide. Perturbation of FMRFamide-activated metabolites of the arachidonic acid pathway in RPeD1 not only prevented FMRFamide-induced suppression of transmitter release from the giant dopamine cell but also shifted the synaptic balance in favor of RPeD1, thus making it the first cell to begin synaptic transmission with VD4 within 12-18 h. A single RPeD1 that had developed dopamine secretory capabilities overnight and was subsequently paired with VD4 for 12-18 h was, however, immune to VD4-induced suppression of transmitter release. Under these experimental conditions, both cells developed mutual inhibitory synapses concurrently. Taken together, our data provide evidence for novel synaptic interaction between reciprocally connected neurons and underscore the importance of transmitter-receptor interplay in regulating the timing of synapse formation in the nervous system.
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收藏
页码:1328 / 1338
页数:11
相关论文
共 50 条
[1]   2 ENDOGENOUS NEUROPEPTIDES MODULATE THE GILL AND SIPHON WITHDRAWAL REFLEX IN APLYSIA BY PRESYNAPTIC FACILITATION INVOLVING CAMP-DEPENDENT CLOSURE OF A SEROTONIN-SENSITIVE POTASSIUM CHANNEL [J].
ABRAMS, TW ;
CASTELLUCCI, VF ;
CAMARDO, JS ;
KANDEL, ER ;
LLOYD, PE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (24) :7956-7960
[2]   Neural science: A century of progress and the mysteries that remain (Reprinted from Cell, vol 1000, pg S1-S55, 2000) [J].
Albright, TD ;
Jessell, TM ;
Kandel, ER ;
Posner, MI .
NEURON, 2000, 25 :S1-S55
[3]  
Asmus SE, 2000, J NEUROSCI, V20, P1495
[4]   A LIPOXYGENASE PATHWAY OF ARACHIDONIC-ACID METABOLISM MEDIATES FMRFAMIDE ACTIVATION OF A POTASSIUM CURRENT IN AN IDENTIFIED NEURON OF HELISOMA [J].
BAHLS, FH ;
RICHMOND, JE ;
SMITH, WL ;
HAYDON, PG .
NEUROSCIENCE LETTERS, 1992, 138 (01) :165-168
[5]   FMRFAMIDE PRODUCES BIPHASIC MODULATION OF THE LFS MOTOR-NEURONS IN THE NEURAL CIRCUIT OF THE SIPHON WITHDRAWAL REFLEX OF APLYSIA BY ACTIVATING NA+ AND K+ CURRENTS [J].
BELKIN, KJ ;
ABRAMS, TW .
JOURNAL OF NEUROSCIENCE, 1993, 13 (12) :5139-5152
[6]  
Belkin KJ, 1998, J EXP BIOL, V201, P2225
[7]  
CHOW I, 1985, J NEUROSCI, V5, P1076
[8]  
CONSTANTINEPATON M, 1990, COLD SPRING HARB SYM, V55, P431
[9]   MODULATORY EFFECTS OF SEROTONIN, FMRFAMIDE, AND MYOMODULIN ON THE DURATION OF ACTION-POTENTIALS, EXCITABILITY, AND MEMBRANE CURRENTS IN TAIL SENSORY NEURONS OF APLYSIA [J].
CRITZ, SD ;
BAXTER, DA ;
BYRNE, JH .
JOURNAL OF NEUROPHYSIOLOGY, 1991, 66 (06) :1912-1926
[10]   HEBBIAN DEPRESSION OF ISOLATED NEUROMUSCULAR SYNAPSES INVITRO [J].
DAN, Y ;
POO, MM .
SCIENCE, 1992, 256 (5063) :1570-1573