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Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions
It is widely assumed that electrical synapses in the mammalian brain, especially between interneurons, underlie neuronal synchrony. In the hippocampus, principal cells also establish electrical synapses with each other and have also been implicated in network oscillations, whereby the origin of fast...
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Published in: | The Journal of neuroscience 2020-06, Vol.40 (24), p.4661-4672 |
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description | It is widely assumed that electrical synapses in the mammalian brain, especially between interneurons, underlie neuronal synchrony. In the hippocampus, principal cells also establish electrical synapses with each other and have also been implicated in network oscillations, whereby the origin of fast electrical activity has been attributed to ectopic spikelets and dendro-dendritic or axo-axonal gap junctions. However, if electrical synapses were in axo-dendritic connections, where chemical synapses occur, the synaptic events would be mixed, having an electrical component preceding the chemical one. This type of communication is less well studied, mainly because it is not easily detected. Moreover, a possible scenario could be that an electrical synapse coexisted with a chemical one, but in a nonconductive state; hence, it would be considered inexistent. Could chemical synapses have a quiescent electrical component? If so, can silent electrical synapses be activated to be detected? We addressed this possibility, and we here report that, indeed, the connexin-36-containing glutamatergic mossy fiber synapses of the rat hippocampus express previously unrecognized electrical synapses, which are normally silent. We reveal that these synapses are pH sensitive, actuate
and
, and that the electrical signaling is bidirectional. With the simultaneous recording of hundreds of cells, we could reveal the existence of an electrical circuit in the hippocampus of adult rats of either sex consisting of principal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-use gap junctions.
In this work, we present a series of experiments, both
and
, that reveal previously unrecognized silent pH-sensitive electrical synapses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber synapse of the hippocampus. This type of connectivity underlies an "electrical circuit" between two substructures of the adult rat hippocampus consisting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-use gap junctions. Its identification will allow us to explore the participation of such a circuit in physiological and pathophysiological functions and will provide valuable conceptual tools to understanding computational and regulatory mechanisms that may underlie network activity. |
doi_str_mv | 10.1523/JNEUROSCI.2590-19.2020 |
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and
, and that the electrical signaling is bidirectional. With the simultaneous recording of hundreds of cells, we could reveal the existence of an electrical circuit in the hippocampus of adult rats of either sex consisting of principal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-use gap junctions.
In this work, we present a series of experiments, both
and
, that reveal previously unrecognized silent pH-sensitive electrical synapses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber synapse of the hippocampus. This type of connectivity underlies an "electrical circuit" between two substructures of the adult rat hippocampus consisting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-use gap junctions. Its identification will allow us to explore the participation of such a circuit in physiological and pathophysiological functions and will provide valuable conceptual tools to understanding computational and regulatory mechanisms that may underlie network activity.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.2590-19.2020</identifier><identifier>PMID: 32393538</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Animals ; Cells, Cultured ; Circuits ; Electric components ; Electrical junctions ; Electrical Synapses - metabolism ; Electrical Synapses - physiology ; Gap junctions ; Gap Junctions - metabolism ; Gap Junctions - physiology ; Glutamatergic transmission ; Glutamic Acid - metabolism ; Hippocampus ; Hippocampus - metabolism ; Hippocampus - physiology ; Interneurons ; Male ; Nerve Net - metabolism ; Nerve Net - physiology ; Neurons - metabolism ; Neurons - physiology ; Oscillations ; Rats ; Rats, Sprague-Dawley ; Rats, Wistar ; Synapses ; Synaptic Transmission - physiology</subject><ispartof>The Journal of neuroscience, 2020-06, Vol.40 (24), p.4661-4672</ispartof><rights>Copyright © 2020 the authors.</rights><rights>Copyright Society for Neuroscience Jun 10, 2020</rights><rights>Copyright © 2020 the authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-d8565bb44e05ab4aebc66debed31c224f87635a0fc86674a8ec4ecc4292f88163</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294797/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7294797/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32393538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ixmatlahua, Diana J</creatorcontrib><creatorcontrib>Vizcarra, Bianca</creatorcontrib><creatorcontrib>Gómez-Lira, Gisela</creatorcontrib><creatorcontrib>Romero-Maldonado, Isabel</creatorcontrib><creatorcontrib>Ortiz, Franco</creatorcontrib><creatorcontrib>Rojas-Piloni, Gerardo</creatorcontrib><creatorcontrib>Gutiérrez, Rafael</creatorcontrib><title>Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>It is widely assumed that electrical synapses in the mammalian brain, especially between interneurons, underlie neuronal synchrony. In the hippocampus, principal cells also establish electrical synapses with each other and have also been implicated in network oscillations, whereby the origin of fast electrical activity has been attributed to ectopic spikelets and dendro-dendritic or axo-axonal gap junctions. However, if electrical synapses were in axo-dendritic connections, where chemical synapses occur, the synaptic events would be mixed, having an electrical component preceding the chemical one. This type of communication is less well studied, mainly because it is not easily detected. Moreover, a possible scenario could be that an electrical synapse coexisted with a chemical one, but in a nonconductive state; hence, it would be considered inexistent. Could chemical synapses have a quiescent electrical component? If so, can silent electrical synapses be activated to be detected? We addressed this possibility, and we here report that, indeed, the connexin-36-containing glutamatergic mossy fiber synapses of the rat hippocampus express previously unrecognized electrical synapses, which are normally silent. We reveal that these synapses are pH sensitive, actuate
and
, and that the electrical signaling is bidirectional. With the simultaneous recording of hundreds of cells, we could reveal the existence of an electrical circuit in the hippocampus of adult rats of either sex consisting of principal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-use gap junctions.
In this work, we present a series of experiments, both
and
, that reveal previously unrecognized silent pH-sensitive electrical synapses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber synapse of the hippocampus. This type of connectivity underlies an "electrical circuit" between two substructures of the adult rat hippocampus consisting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-use gap junctions. Its identification will allow us to explore the participation of such a circuit in physiological and pathophysiological functions and will provide valuable conceptual tools to understanding computational and regulatory mechanisms that may underlie network activity.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Circuits</subject><subject>Electric components</subject><subject>Electrical junctions</subject><subject>Electrical Synapses - metabolism</subject><subject>Electrical Synapses - physiology</subject><subject>Gap junctions</subject><subject>Gap Junctions - metabolism</subject><subject>Gap Junctions - physiology</subject><subject>Glutamatergic transmission</subject><subject>Glutamic Acid - metabolism</subject><subject>Hippocampus</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - physiology</subject><subject>Interneurons</subject><subject>Male</subject><subject>Nerve Net - metabolism</subject><subject>Nerve Net - physiology</subject><subject>Neurons - metabolism</subject><subject>Neurons - physiology</subject><subject>Oscillations</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rats, Wistar</subject><subject>Synapses</subject><subject>Synaptic Transmission - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpdkU9P3DAQxa2qVdlu-xWQpV56ydb_EieXSnS13YLQIkERBw6W40zA1BsvtgPi29cRdNVyGsnz5s34_RA6pGRBS8a_nmxWl-dnF8vjBSsbUtBmwQgjb9Asd5uCCULfohlhkhSVkOIAfYjxjhAiCZXv0QFnvOElr2foegNj8IN2eO3GpLc6QbixBm8gPfrwG68cmBSs0c494SsboMOPNt3iC-tgSPj7mPCRSfZBJ906wGu9wyfjkF_8ED-id712ET691Dm6_LH6tfxZnJ6tj5dHp4URgqWiq8uqbFshgJS6FRpaU1UdtNBxahgTfS0rXmrSm7qqpNA1GAHGCNawvq5pxefo27Pvbmy30Jl8WNBO7YLd6vCkvLbq_85gb9WNf1CSNUI2Mht8eTEI_n6EmNTWRgPO6QH8GNUUZ814XpWln19J7_wYcn6TinJaSpqjnaPqWWWCjzFAvz-GEjXxU3t-auKnaKMmfnnw8N-v7Mf-AuN_AD8hmTs</recordid><startdate>20200610</startdate><enddate>20200610</enddate><creator>Ixmatlahua, Diana J</creator><creator>Vizcarra, Bianca</creator><creator>Gómez-Lira, Gisela</creator><creator>Romero-Maldonado, Isabel</creator><creator>Ortiz, Franco</creator><creator>Rojas-Piloni, Gerardo</creator><creator>Gutiérrez, Rafael</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200610</creationdate><title>Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions</title><author>Ixmatlahua, Diana J ; Vizcarra, Bianca ; Gómez-Lira, Gisela ; Romero-Maldonado, Isabel ; Ortiz, Franco ; Rojas-Piloni, Gerardo ; Gutiérrez, Rafael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-d8565bb44e05ab4aebc66debed31c224f87635a0fc86674a8ec4ecc4292f88163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Circuits</topic><topic>Electric components</topic><topic>Electrical junctions</topic><topic>Electrical Synapses - metabolism</topic><topic>Electrical Synapses - physiology</topic><topic>Gap junctions</topic><topic>Gap Junctions - metabolism</topic><topic>Gap Junctions - physiology</topic><topic>Glutamatergic transmission</topic><topic>Glutamic Acid - metabolism</topic><topic>Hippocampus</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - physiology</topic><topic>Interneurons</topic><topic>Male</topic><topic>Nerve Net - metabolism</topic><topic>Nerve Net - physiology</topic><topic>Neurons - metabolism</topic><topic>Neurons - physiology</topic><topic>Oscillations</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rats, Wistar</topic><topic>Synapses</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ixmatlahua, Diana J</creatorcontrib><creatorcontrib>Vizcarra, Bianca</creatorcontrib><creatorcontrib>Gómez-Lira, Gisela</creatorcontrib><creatorcontrib>Romero-Maldonado, Isabel</creatorcontrib><creatorcontrib>Ortiz, Franco</creatorcontrib><creatorcontrib>Rojas-Piloni, Gerardo</creatorcontrib><creatorcontrib>Gutiérrez, Rafael</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ixmatlahua, Diana J</au><au>Vizcarra, Bianca</au><au>Gómez-Lira, Gisela</au><au>Romero-Maldonado, Isabel</au><au>Ortiz, Franco</au><au>Rojas-Piloni, Gerardo</au><au>Gutiérrez, Rafael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2020-06-10</date><risdate>2020</risdate><volume>40</volume><issue>24</issue><spage>4661</spage><epage>4672</epage><pages>4661-4672</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>It is widely assumed that electrical synapses in the mammalian brain, especially between interneurons, underlie neuronal synchrony. In the hippocampus, principal cells also establish electrical synapses with each other and have also been implicated in network oscillations, whereby the origin of fast electrical activity has been attributed to ectopic spikelets and dendro-dendritic or axo-axonal gap junctions. However, if electrical synapses were in axo-dendritic connections, where chemical synapses occur, the synaptic events would be mixed, having an electrical component preceding the chemical one. This type of communication is less well studied, mainly because it is not easily detected. Moreover, a possible scenario could be that an electrical synapse coexisted with a chemical one, but in a nonconductive state; hence, it would be considered inexistent. Could chemical synapses have a quiescent electrical component? If so, can silent electrical synapses be activated to be detected? We addressed this possibility, and we here report that, indeed, the connexin-36-containing glutamatergic mossy fiber synapses of the rat hippocampus express previously unrecognized electrical synapses, which are normally silent. We reveal that these synapses are pH sensitive, actuate
and
, and that the electrical signaling is bidirectional. With the simultaneous recording of hundreds of cells, we could reveal the existence of an electrical circuit in the hippocampus of adult rats of either sex consisting of principal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-use gap junctions.
In this work, we present a series of experiments, both
and
, that reveal previously unrecognized silent pH-sensitive electrical synapses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber synapse of the hippocampus. This type of connectivity underlies an "electrical circuit" between two substructures of the adult rat hippocampus consisting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-use gap junctions. Its identification will allow us to explore the participation of such a circuit in physiological and pathophysiological functions and will provide valuable conceptual tools to understanding computational and regulatory mechanisms that may underlie network activity.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>32393538</pmid><doi>10.1523/JNEUROSCI.2590-19.2020</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cells, Cultured Circuits Electric components Electrical junctions Electrical Synapses - metabolism Electrical Synapses - physiology Gap junctions Gap Junctions - metabolism Gap Junctions - physiology Glutamatergic transmission Glutamic Acid - metabolism Hippocampus Hippocampus - metabolism Hippocampus - physiology Interneurons Male Nerve Net - metabolism Nerve Net - physiology Neurons - metabolism Neurons - physiology Oscillations Rats Rats, Sprague-Dawley Rats, Wistar Synapses Synaptic Transmission - physiology |
title | Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions |
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