Synapse (New York, N.Y.) · 2005
Correlation of non-uniform protein expression with variation in transmitter release probability.
Сравнительное исследованиеСтатьяНазвание и аннотация: Перевод в очереди
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Knight David, Mann Dwayne L, Jackson V Margaret, Trout Stephen J, Cunnane Tom C, Lavidis Nickolas A
Аннотация
The strength of synaptic transmission is highly variable between different synapses. The present study examined some factors that may contribute to this variation in the strength of neurotransmission in sympathetic varicosities of the mouse vas deferens. Transmitter release was measured using a focal macropatch electrode placed over pairs of visualised varicosities. By regulating the calcium concentration of the solutions inside the recording electrode and in the bath independently of each other, transmitter release was restricted to one or two surface varicosities at each recording site. Using this technique, transmitter release probability was shown to be highly variable, even between adjacent varicosities on single axon branches. Very little variation was observed in the calcium influx following single impulse nerve stimulation between adjacent Oregon Green BAPTA-1 loaded varicosities. However, the staining intensities of three vesicular proteins, SV2, synaptophysin, and synaptotagmin 1, showed considerable variation between adjacent varicosities on single axon branches. This variation in staining intensity may be partly explained by variation in the density of synaptic vesicles. However, double staining experiments using two vesicular antigens showed some varicosities staining for one vesicular antigen, but not for the second, suggesting that the expression of these release machinery proteins is regulated locally within the varicosities. The results of the present study strengthen suggestions that synaptic strength is at least in part, regulated by variation in the expression of vesicular proteins.
Предметные рубрики MeSH
Action PotentialsAnimalsCalciumCalcium-Binding ProteinsEgtazic AcidElectric StimulationElectrophysiologyImmunohistochemistryIn Vitro TechniquesIndicators and ReagentsMaleMembrane GlycoproteinsMiceMice, Inbred BALB CMicroscopy, Electron, TransmissionNerve Tissue ProteinsNeurotransmitter AgentsProbabilitySynapsesSynaptic TransmissionSynaptic VesiclesSynaptophysinSynaptotagmin ISynaptotagminsVas Deferens