<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>110(24)</volume><submitter>Aldahabi M</submitter><pubmed_abstract>A stunning example of synaptic diversity is the postsynaptic target cell-type-dependent difference in synaptic efficacy in cortical networks. Here, we show that CA1 pyramidal cell (PC) to fast spiking interneuron (FSIN) connections have 10-fold larger release probability (P&lt;sub>v&lt;/sub>) than those on oriens lacunosum-moleculare (O-LM) interneurons. Freeze-fracture immunolabeling revealed that different nano-topologies and coupling distances between Ca&lt;sup>2+&lt;/sup> channels and release sites (RSs) are not responsible for the distinct P&lt;sub>v&lt;/sub>. Although [Ca&lt;sup>2+&lt;/sup>] transients are 40% larger in FSINs innervating boutons, when [Ca&lt;sup>2+&lt;/sup>] entry is matched in the two bouton populations, EPSCs in O-LM cells are still 7-fold smaller. However, application of a phorbol ester analog</pubmed_abstract><journal>Neuron</journal><pagination>4144-4161.e7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9796815</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Different priming states of synaptic vesicles underlie distinct release probabilities at hippocampal excitatory synapses.</pubmed_title><pmcid>PMC9796815</pmcid><pubmed_authors>Holderith N</pubmed_authors><pubmed_authors>Aldahabi M</pubmed_authors><pubmed_authors>Balint F</pubmed_authors><pubmed_authors>Reva M</pubmed_authors><pubmed_authors>Nusser Z</pubmed_authors><pubmed_authors>Lorincz A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Different priming states of synaptic vesicles underlie distinct release probabilities at hippocampal excitatory synapses.</name><description>A stunning example of synaptic diversity is the postsynaptic target cell-type-dependent difference in synaptic efficacy in cortical networks. Here, we show that CA1 pyramidal cell (PC) to fast spiking interneuron (FSIN) connections have 10-fold larger release probability (P&lt;sub>v&lt;/sub>) than those on oriens lacunosum-moleculare (O-LM) interneurons. Freeze-fracture immunolabeling revealed that different nano-topologies and coupling distances between Ca&lt;sup>2+&lt;/sup> channels and release sites (RSs) are not responsible for the distinct P&lt;sub>v&lt;/sub>. Although [Ca&lt;sup>2+&lt;/sup>] transients are 40% larger in FSINs innervating boutons, when [Ca&lt;sup>2+&lt;/sup>] entry is matched in the two bouton populations, EPSCs in O-LM cells are still 7-fold smaller. However, application of a phorbol ester analog</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-22T18:00:55.175Z</modification><creation>2025-04-06T02:20:16.164Z</creation></dates><accession>S-EPMC9796815</accession><cross_references><pubmed>36261033</pubmed><doi>10.1016/j.neuron.2022.09.035</doi></cross_references></HashMap>