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Coincidence Detection within the Excitable Rat Olfactory Bulb Granule Cell Spines
In the mammalian olfactory bulb, the inhibitory axonless granule cells (GCs) feature reciprocal synapses that interconnect them with the principal neurons of the bulb, mitral, and tufted cells. These synapses are located within large excitable spines that can generate local action potentials (APs) u...
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Published in: | The Journal of neuroscience 2019-01, Vol.39 (4), p.584-595 |
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description | In the mammalian olfactory bulb, the inhibitory axonless granule cells (GCs) feature reciprocal synapses that interconnect them with the principal neurons of the bulb, mitral, and tufted cells. These synapses are located within large excitable spines that can generate local action potentials (APs) upon synaptic input ("spine spike"). Moreover, GCs can fire global APs that propagate throughout the dendrite. Strikingly, local postsynaptic Ca
entry summates mostly linearly with Ca
entry due to coincident global APs generated by glomerular stimulation, although some underlying conductances should be inactivated. We investigated this phenomenon by constructing a compartmental GC model to simulate the pairing of local and global signals as a function of their temporal separation Δt. These simulations yield strongly sublinear summation of spine Ca
entry for the case of perfect coincidence Δt = 0 ms. Summation efficiency (SE) sharply rises for both positive and negative Δt. The SE reduction for coincident signals depends on the presence of voltage-gated Na
channels in the spine head, while NMDARs are not essential. We experimentally validated the simulated SE in slices of juvenile rat brain (both sexes) by pairing two-photon uncaging of glutamate at spines and APs evoked by somatic current injection at various intervals Δt while imaging spine Ca
signals. Finally, the latencies of synaptically evoked global APs and EPSPs were found to correspond to Δt ≈ 10 ms, explaining the observed approximately linear summation of synaptic local and global signals. Our results provide additional evidence for the existence of the GC spine spike.
Here we investigate the interaction of local synaptic inputs and global activation of a neuron by a backpropagating action potential within a dendritic spine with respect to local Ca
signaling. Our system of interest, the reciprocal spine of the olfactory bulb granule cell, is known to feature a special processing mode, namely, a synaptically triggered action potential that is restricted to the spine head. Therefore, coincidence detection of local and global signals follows different rules than in more conventional synapses. We unravel these rules using both simulations and experiments and find that signals coincident within ≈±7 ms around 0 ms result in sublinear summation of Ca
entry because of synaptic activation of voltage-gated Na
channels within the spine. |
doi_str_mv | 10.1523/JNEUROSCI.1798-18.2018 |
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entry summates mostly linearly with Ca
entry due to coincident global APs generated by glomerular stimulation, although some underlying conductances should be inactivated. We investigated this phenomenon by constructing a compartmental GC model to simulate the pairing of local and global signals as a function of their temporal separation Δt. These simulations yield strongly sublinear summation of spine Ca
entry for the case of perfect coincidence Δt = 0 ms. Summation efficiency (SE) sharply rises for both positive and negative Δt. The SE reduction for coincident signals depends on the presence of voltage-gated Na
channels in the spine head, while NMDARs are not essential. We experimentally validated the simulated SE in slices of juvenile rat brain (both sexes) by pairing two-photon uncaging of glutamate at spines and APs evoked by somatic current injection at various intervals Δt while imaging spine Ca
signals. Finally, the latencies of synaptically evoked global APs and EPSPs were found to correspond to Δt ≈ 10 ms, explaining the observed approximately linear summation of synaptic local and global signals. Our results provide additional evidence for the existence of the GC spine spike.
Here we investigate the interaction of local synaptic inputs and global activation of a neuron by a backpropagating action potential within a dendritic spine with respect to local Ca
signaling. Our system of interest, the reciprocal spine of the olfactory bulb granule cell, is known to feature a special processing mode, namely, a synaptically triggered action potential that is restricted to the spine head. Therefore, coincidence detection of local and global signals follows different rules than in more conventional synapses. We unravel these rules using both simulations and experiments and find that signals coincident within ≈±7 ms around 0 ms result in sublinear summation of Ca
entry because of synaptic activation of voltage-gated Na
channels within the spine.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.1798-18.2018</identifier><identifier>PMID: 30674614</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Action Potentials - physiology ; Algorithms ; Animals ; Brain ; Brain slice preparation ; Calcium imaging ; Calcium influx ; Calcium ions ; Calcium Signaling - physiology ; Calcium signalling ; Computer Simulation ; Current injection ; Dendrites - physiology ; Dendritic spines ; Dendritic structure ; Excitatory Postsynaptic Potentials - physiology ; Female ; Glutamic acid receptors ; Granular materials ; Granule cells ; Male ; Models, Neurological ; N-Methyl-D-aspartic acid receptors ; Neuroimaging ; Neurons - physiology ; Olfactory bulb ; Olfactory Bulb - cytology ; Rats ; Rats, Wistar ; Receptors, N-Methyl-D-Aspartate - metabolism ; Sodium channels ; Sodium channels (voltage-gated) ; Sodium Channels - physiology ; Spine ; Synapses</subject><ispartof>The Journal of neuroscience, 2019-01, Vol.39 (4), p.584-595</ispartof><rights>Copyright © 2019 the authors 0270-6474/19/390584-12$15.00/0.</rights><rights>Copyright Society for Neuroscience Jan 23, 2019</rights><rights>Copyright © 2019 the authors 0270-6474/19/390584-12$15.00/0 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-703cb6c02ef9e9ad456a0e62afedaeba280c1a449971d47ebf48721f242b67b23</citedby><cites>FETCH-LOGICAL-c508t-703cb6c02ef9e9ad456a0e62afedaeba280c1a449971d47ebf48721f242b67b23</cites><orcidid>0000-0003-4737-5267 ; 0000-0002-5283-263X ; 0000-0002-5869-8523</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343640/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343640/$$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/30674614$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aghvami, S Sara</creatorcontrib><creatorcontrib>Müller, Max</creatorcontrib><creatorcontrib>Araabi, Babak N</creatorcontrib><creatorcontrib>Egger, Veronica</creatorcontrib><title>Coincidence Detection within the Excitable Rat Olfactory Bulb Granule Cell Spines</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>In the mammalian olfactory bulb, the inhibitory axonless granule cells (GCs) feature reciprocal synapses that interconnect them with the principal neurons of the bulb, mitral, and tufted cells. These synapses are located within large excitable spines that can generate local action potentials (APs) upon synaptic input ("spine spike"). Moreover, GCs can fire global APs that propagate throughout the dendrite. Strikingly, local postsynaptic Ca
entry summates mostly linearly with Ca
entry due to coincident global APs generated by glomerular stimulation, although some underlying conductances should be inactivated. We investigated this phenomenon by constructing a compartmental GC model to simulate the pairing of local and global signals as a function of their temporal separation Δt. These simulations yield strongly sublinear summation of spine Ca
entry for the case of perfect coincidence Δt = 0 ms. Summation efficiency (SE) sharply rises for both positive and negative Δt. The SE reduction for coincident signals depends on the presence of voltage-gated Na
channels in the spine head, while NMDARs are not essential. We experimentally validated the simulated SE in slices of juvenile rat brain (both sexes) by pairing two-photon uncaging of glutamate at spines and APs evoked by somatic current injection at various intervals Δt while imaging spine Ca
signals. Finally, the latencies of synaptically evoked global APs and EPSPs were found to correspond to Δt ≈ 10 ms, explaining the observed approximately linear summation of synaptic local and global signals. Our results provide additional evidence for the existence of the GC spine spike.
Here we investigate the interaction of local synaptic inputs and global activation of a neuron by a backpropagating action potential within a dendritic spine with respect to local Ca
signaling. Our system of interest, the reciprocal spine of the olfactory bulb granule cell, is known to feature a special processing mode, namely, a synaptically triggered action potential that is restricted to the spine head. Therefore, coincidence detection of local and global signals follows different rules than in more conventional synapses. We unravel these rules using both simulations and experiments and find that signals coincident within ≈±7 ms around 0 ms result in sublinear summation of Ca
entry because of synaptic activation of voltage-gated Na
channels within the spine.</description><subject>Action Potentials - physiology</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Brain</subject><subject>Brain slice preparation</subject><subject>Calcium imaging</subject><subject>Calcium influx</subject><subject>Calcium ions</subject><subject>Calcium Signaling - physiology</subject><subject>Calcium signalling</subject><subject>Computer Simulation</subject><subject>Current injection</subject><subject>Dendrites - physiology</subject><subject>Dendritic spines</subject><subject>Dendritic structure</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Female</subject><subject>Glutamic acid receptors</subject><subject>Granular materials</subject><subject>Granule cells</subject><subject>Male</subject><subject>Models, Neurological</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>Neuroimaging</subject><subject>Neurons - physiology</subject><subject>Olfactory bulb</subject><subject>Olfactory Bulb - cytology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Sodium channels</subject><subject>Sodium channels (voltage-gated)</subject><subject>Sodium Channels - physiology</subject><subject>Spine</subject><subject>Synapses</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkU9vEzEQxS1UREPhK1SWeullg__F3r1UapdQiioiWnq2vN7ZxtXGDrYX6LfHUUtUOM3h_eZp3jyEjimZ0wXjH758Xd7drG7bqzlVTV3Res4IrV-hWVGbiglCD9CMMEUqKZQ4RG9TeiCEKELVG3TIiVRCUjFD39rgvHU9eAv4I2Sw2QWPf7m8dh7nNeDlb-uy6UbANybj1TgYm0N8xBfT2OHLaPxUpBbGEd9unYf0Dr0ezJjg_fM8Qneflt_bz9X16vKqPb-u7ILUuVKE205awmBooDG9WEhDQDIzQG-gM6wmlhohmkbRXijoBlErRgcmWCdVx_gROnvy3U7dBnoLPkcz6m10GxMfdTBO_6t4t9b34aeWXHApSDE4fTaI4ccEKeuNS7YEMR7ClDQrnxWC0kVT0JP_0IcwRV_i7ShGOadCFko-UTaGlCIM-2Mo0bvW9L41vWtN01rvWiuLxy-j7Nf-1sT_AF_flMc</recordid><startdate>20190123</startdate><enddate>20190123</enddate><creator>Aghvami, S Sara</creator><creator>Müller, Max</creator><creator>Araabi, Babak N</creator><creator>Egger, Veronica</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><orcidid>https://orcid.org/0000-0003-4737-5267</orcidid><orcidid>https://orcid.org/0000-0002-5283-263X</orcidid><orcidid>https://orcid.org/0000-0002-5869-8523</orcidid></search><sort><creationdate>20190123</creationdate><title>Coincidence Detection within the Excitable Rat Olfactory Bulb Granule Cell Spines</title><author>Aghvami, S Sara ; Müller, Max ; Araabi, Babak N ; Egger, Veronica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-703cb6c02ef9e9ad456a0e62afedaeba280c1a449971d47ebf48721f242b67b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Action Potentials - physiology</topic><topic>Algorithms</topic><topic>Animals</topic><topic>Brain</topic><topic>Brain slice preparation</topic><topic>Calcium imaging</topic><topic>Calcium influx</topic><topic>Calcium ions</topic><topic>Calcium Signaling - physiology</topic><topic>Calcium signalling</topic><topic>Computer Simulation</topic><topic>Current injection</topic><topic>Dendrites - physiology</topic><topic>Dendritic spines</topic><topic>Dendritic structure</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Female</topic><topic>Glutamic acid receptors</topic><topic>Granular materials</topic><topic>Granule cells</topic><topic>Male</topic><topic>Models, Neurological</topic><topic>N-Methyl-D-aspartic acid receptors</topic><topic>Neuroimaging</topic><topic>Neurons - physiology</topic><topic>Olfactory bulb</topic><topic>Olfactory Bulb - cytology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Sodium channels</topic><topic>Sodium channels (voltage-gated)</topic><topic>Sodium Channels - physiology</topic><topic>Spine</topic><topic>Synapses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aghvami, S Sara</creatorcontrib><creatorcontrib>Müller, Max</creatorcontrib><creatorcontrib>Araabi, Babak N</creatorcontrib><creatorcontrib>Egger, Veronica</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>Aghvami, S Sara</au><au>Müller, Max</au><au>Araabi, Babak N</au><au>Egger, Veronica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coincidence Detection within the Excitable Rat Olfactory Bulb Granule Cell Spines</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2019-01-23</date><risdate>2019</risdate><volume>39</volume><issue>4</issue><spage>584</spage><epage>595</epage><pages>584-595</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>In the mammalian olfactory bulb, the inhibitory axonless granule cells (GCs) feature reciprocal synapses that interconnect them with the principal neurons of the bulb, mitral, and tufted cells. These synapses are located within large excitable spines that can generate local action potentials (APs) upon synaptic input ("spine spike"). Moreover, GCs can fire global APs that propagate throughout the dendrite. Strikingly, local postsynaptic Ca
entry summates mostly linearly with Ca
entry due to coincident global APs generated by glomerular stimulation, although some underlying conductances should be inactivated. We investigated this phenomenon by constructing a compartmental GC model to simulate the pairing of local and global signals as a function of their temporal separation Δt. These simulations yield strongly sublinear summation of spine Ca
entry for the case of perfect coincidence Δt = 0 ms. Summation efficiency (SE) sharply rises for both positive and negative Δt. The SE reduction for coincident signals depends on the presence of voltage-gated Na
channels in the spine head, while NMDARs are not essential. We experimentally validated the simulated SE in slices of juvenile rat brain (both sexes) by pairing two-photon uncaging of glutamate at spines and APs evoked by somatic current injection at various intervals Δt while imaging spine Ca
signals. Finally, the latencies of synaptically evoked global APs and EPSPs were found to correspond to Δt ≈ 10 ms, explaining the observed approximately linear summation of synaptic local and global signals. Our results provide additional evidence for the existence of the GC spine spike.
Here we investigate the interaction of local synaptic inputs and global activation of a neuron by a backpropagating action potential within a dendritic spine with respect to local Ca
signaling. Our system of interest, the reciprocal spine of the olfactory bulb granule cell, is known to feature a special processing mode, namely, a synaptically triggered action potential that is restricted to the spine head. Therefore, coincidence detection of local and global signals follows different rules than in more conventional synapses. We unravel these rules using both simulations and experiments and find that signals coincident within ≈±7 ms around 0 ms result in sublinear summation of Ca
entry because of synaptic activation of voltage-gated Na
channels within the spine.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>30674614</pmid><doi>10.1523/JNEUROSCI.1798-18.2018</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4737-5267</orcidid><orcidid>https://orcid.org/0000-0002-5283-263X</orcidid><orcidid>https://orcid.org/0000-0002-5869-8523</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials - physiology Algorithms Animals Brain Brain slice preparation Calcium imaging Calcium influx Calcium ions Calcium Signaling - physiology Calcium signalling Computer Simulation Current injection Dendrites - physiology Dendritic spines Dendritic structure Excitatory Postsynaptic Potentials - physiology Female Glutamic acid receptors Granular materials Granule cells Male Models, Neurological N-Methyl-D-aspartic acid receptors Neuroimaging Neurons - physiology Olfactory bulb Olfactory Bulb - cytology Rats Rats, Wistar Receptors, N-Methyl-D-Aspartate - metabolism Sodium channels Sodium channels (voltage-gated) Sodium Channels - physiology Spine Synapses |
title | Coincidence Detection within the Excitable Rat Olfactory Bulb Granule Cell Spines |
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