Mouse subthalamic nucleus neurons with local axon collaterals
The neuronal population of the subthalamic nucleus (STN) has the ability to prolong incoming cortical excitation. This could result from intra‐STN feedback excitation. The combination of inducible genetic fate mapping techniques with in vitro targeted patch‐clamp recordings, allowed identifying a ne...
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Veröffentlicht in: | Journal of comparative neurology (1911) 2018-02, Vol.526 (2), p.275-284 |
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container_title | Journal of comparative neurology (1911) |
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description | The neuronal population of the subthalamic nucleus (STN) has the ability to prolong incoming cortical excitation. This could result from intra‐STN feedback excitation. The combination of inducible genetic fate mapping techniques with in vitro targeted patch‐clamp recordings, allowed identifying a new type of STN neurons that possess a highly collateralized intrinsic axon. The time window of birth dates was found to be narrow (E10.5–E14.5) with very few STN neurons born at E10.5 or E14.5. The fate mapped E11.5–12.5 STN neuronal population included 20% of neurons with profuse axonal branching inside the nucleus and a dendritic arbor that differed from that of STN neurons without local axon collaterals. They had intrinsic electrophysiological properties and in particular, the ability to generate plateau potentials, similar to that of STN neurons without local axon collaterals and more generally to that of classically described STN neurons. This suggests that a subpopulation of STN neurons forms a local glutamatergic network, which together with plateau potentials, allow amplification of hyperdirect cortical inputs and synchronization of the STN neuronal population.
The combination of inducible genetic fate mapping techniques and in vitro targeted patch‐clamp recordings demonstrated the existence of a new type of mouse subthalamic nucleus (STN) neuron that possesses a highly local collateralized axon. These neurons represent twenty percent of fate mapped E11.5–12.5 STN neurons, exhibit different dendritic arbors compared to non‐collateralized STN neurons and have electrophysiological properties similar to that of the general STN population. They are well‐suited to participate to a feed forward excitatory network in the STN. |
doi_str_mv | 10.1002/cne.24334 |
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The combination of inducible genetic fate mapping techniques and in vitro targeted patch‐clamp recordings demonstrated the existence of a new type of mouse subthalamic nucleus (STN) neuron that possesses a highly local collateralized axon. These neurons represent twenty percent of fate mapped E11.5–12.5 STN neurons, exhibit different dendritic arbors compared to non‐collateralized STN neurons and have electrophysiological properties similar to that of the general STN population. They are well‐suited to participate to a feed forward excitatory network in the STN.</description><identifier>ISSN: 0021-9967</identifier><identifier>ISSN: 0092-7317</identifier><identifier>EISSN: 1096-9861</identifier><identifier>EISSN: 1550-7130</identifier><identifier>DOI: 10.1002/cne.24334</identifier><identifier>PMID: 28971478</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Axon collaterals ; basal ganglia ; calcium binding proteins ; Cell fate ; Cortex ; Electrical stimuli ; Fate maps ; Gene mapping ; Glutamatergic transmission ; inducible genetic fate mapping ; Life Sciences ; Neurons ; Neurons and Cognition ; patch‐clamp ; Placebo effect ; Rodents ; RRID: AB_10000340 ; RRID: AB_10000342 ; RRID: AB_2313584 ; RRID: AB_2336933 ; RRID: AB_2337249 ; RRID: AB_2650496 ; Solitary tract nucleus ; Subthalamic nucleus ; Synchronization</subject><ispartof>Journal of comparative neurology (1911), 2018-02, Vol.526 (2), p.275-284</ispartof><rights>2017 Wiley Periodicals, Inc.</rights><rights>2018 Wiley Periodicals, Inc.</rights><rights>Attribution</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4224-b82bb34837e4f3f1fa026d95702f7c26125c756753474d5236eec92d994efde93</citedby><cites>FETCH-LOGICAL-c4224-b82bb34837e4f3f1fa026d95702f7c26125c756753474d5236eec92d994efde93</cites><orcidid>0000-0002-5545-059X ; 0000-0002-9778-8716 ; 0000-0003-2111-6638</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcne.24334$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.24334$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28971478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://amu.hal.science/hal-01963551$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gouty‐Colomer, Laurie‐Anne</creatorcontrib><creatorcontrib>Michel, François J</creatorcontrib><creatorcontrib>Baude, Agnès</creatorcontrib><creatorcontrib>Lopez‐Pauchet, Catherine</creatorcontrib><creatorcontrib>Dufour, Amandine</creatorcontrib><creatorcontrib>Cossart, Rosa</creatorcontrib><creatorcontrib>Hammond, Constance</creatorcontrib><title>Mouse subthalamic nucleus neurons with local axon collaterals</title><title>Journal of comparative neurology (1911)</title><addtitle>J Comp Neurol</addtitle><description>The neuronal population of the subthalamic nucleus (STN) has the ability to prolong incoming cortical excitation. This could result from intra‐STN feedback excitation. The combination of inducible genetic fate mapping techniques with in vitro targeted patch‐clamp recordings, allowed identifying a new type of STN neurons that possess a highly collateralized intrinsic axon. The time window of birth dates was found to be narrow (E10.5–E14.5) with very few STN neurons born at E10.5 or E14.5. The fate mapped E11.5–12.5 STN neuronal population included 20% of neurons with profuse axonal branching inside the nucleus and a dendritic arbor that differed from that of STN neurons without local axon collaterals. They had intrinsic electrophysiological properties and in particular, the ability to generate plateau potentials, similar to that of STN neurons without local axon collaterals and more generally to that of classically described STN neurons. This suggests that a subpopulation of STN neurons forms a local glutamatergic network, which together with plateau potentials, allow amplification of hyperdirect cortical inputs and synchronization of the STN neuronal population.
The combination of inducible genetic fate mapping techniques and in vitro targeted patch‐clamp recordings demonstrated the existence of a new type of mouse subthalamic nucleus (STN) neuron that possesses a highly local collateralized axon. These neurons represent twenty percent of fate mapped E11.5–12.5 STN neurons, exhibit different dendritic arbors compared to non‐collateralized STN neurons and have electrophysiological properties similar to that of the general STN population. They are well‐suited to participate to a feed forward excitatory network in the STN.</description><subject>Axon collaterals</subject><subject>basal ganglia</subject><subject>calcium binding proteins</subject><subject>Cell fate</subject><subject>Cortex</subject><subject>Electrical stimuli</subject><subject>Fate maps</subject><subject>Gene mapping</subject><subject>Glutamatergic transmission</subject><subject>inducible genetic fate mapping</subject><subject>Life Sciences</subject><subject>Neurons</subject><subject>Neurons and Cognition</subject><subject>patch‐clamp</subject><subject>Placebo effect</subject><subject>Rodents</subject><subject>RRID: AB_10000340</subject><subject>RRID: AB_10000342</subject><subject>RRID: AB_2313584</subject><subject>RRID: AB_2336933</subject><subject>RRID: AB_2337249</subject><subject>RRID: AB_2650496</subject><subject>Solitary tract nucleus</subject><subject>Subthalamic nucleus</subject><subject>Synchronization</subject><issn>0021-9967</issn><issn>0092-7317</issn><issn>1096-9861</issn><issn>1550-7130</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE9PwkAQxTdGI4ge_AKmiRc9FPZfd7sHD4SgmKBe9LzZbqehpHSxS0W-vYsgJiaeJpn55c17D6FLgvsEYzqwNfQpZ4wfoS7BSsQqFeQYdcONxEoJ2UFn3s8xxkqx9BR1aKok4TLtorsn13qIfJutZqYyi9JGdWsraH1UQ9u42kfrcjWLKmdNFZlPV0fWVZVZQWMqf45OijDgYj976O1-_DqaxNOXh8fRcBpbTimPs5RmGeMpk8ALVpDCYCpylUhMC2mpIDSxMhEyYVzyPKFMAFhFc6U4FDko1kO3O93gUS-bcmGajXam1JPhVG93mCjBkoR8kMDe7Nhl495b8Cu9KL2F4LmGkFUTxQWnCVEsoNd_0LlrmzokCZTEXGGe0t_ntnHeN1AcHBCst_3r0L_-7j-wV3vFNltAfiB_Cg_AYAesywo2_yvp0fN4J_kFfHeMNQ</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Gouty‐Colomer, Laurie‐Anne</creator><creator>Michel, François J</creator><creator>Baude, Agnès</creator><creator>Lopez‐Pauchet, Catherine</creator><creator>Dufour, Amandine</creator><creator>Cossart, Rosa</creator><creator>Hammond, Constance</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley & Sons</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-5545-059X</orcidid><orcidid>https://orcid.org/0000-0002-9778-8716</orcidid><orcidid>https://orcid.org/0000-0003-2111-6638</orcidid></search><sort><creationdate>20180201</creationdate><title>Mouse subthalamic nucleus neurons with local axon collaterals</title><author>Gouty‐Colomer, Laurie‐Anne ; Michel, François J ; Baude, Agnès ; Lopez‐Pauchet, Catherine ; Dufour, Amandine ; Cossart, Rosa ; Hammond, Constance</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4224-b82bb34837e4f3f1fa026d95702f7c26125c756753474d5236eec92d994efde93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Axon collaterals</topic><topic>basal ganglia</topic><topic>calcium binding proteins</topic><topic>Cell fate</topic><topic>Cortex</topic><topic>Electrical stimuli</topic><topic>Fate maps</topic><topic>Gene mapping</topic><topic>Glutamatergic transmission</topic><topic>inducible genetic fate mapping</topic><topic>Life Sciences</topic><topic>Neurons</topic><topic>Neurons and Cognition</topic><topic>patch‐clamp</topic><topic>Placebo effect</topic><topic>Rodents</topic><topic>RRID: AB_10000340</topic><topic>RRID: AB_10000342</topic><topic>RRID: AB_2313584</topic><topic>RRID: AB_2336933</topic><topic>RRID: AB_2337249</topic><topic>RRID: AB_2650496</topic><topic>Solitary tract nucleus</topic><topic>Subthalamic nucleus</topic><topic>Synchronization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gouty‐Colomer, Laurie‐Anne</creatorcontrib><creatorcontrib>Michel, François J</creatorcontrib><creatorcontrib>Baude, Agnès</creatorcontrib><creatorcontrib>Lopez‐Pauchet, Catherine</creatorcontrib><creatorcontrib>Dufour, Amandine</creatorcontrib><creatorcontrib>Cossart, Rosa</creatorcontrib><creatorcontrib>Hammond, Constance</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gouty‐Colomer, Laurie‐Anne</au><au>Michel, François J</au><au>Baude, Agnès</au><au>Lopez‐Pauchet, Catherine</au><au>Dufour, Amandine</au><au>Cossart, Rosa</au><au>Hammond, Constance</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mouse subthalamic nucleus neurons with local axon collaterals</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J Comp Neurol</addtitle><date>2018-02-01</date><risdate>2018</risdate><volume>526</volume><issue>2</issue><spage>275</spage><epage>284</epage><pages>275-284</pages><issn>0021-9967</issn><issn>0092-7317</issn><eissn>1096-9861</eissn><eissn>1550-7130</eissn><abstract>The neuronal population of the subthalamic nucleus (STN) has the ability to prolong incoming cortical excitation. This could result from intra‐STN feedback excitation. The combination of inducible genetic fate mapping techniques with in vitro targeted patch‐clamp recordings, allowed identifying a new type of STN neurons that possess a highly collateralized intrinsic axon. The time window of birth dates was found to be narrow (E10.5–E14.5) with very few STN neurons born at E10.5 or E14.5. The fate mapped E11.5–12.5 STN neuronal population included 20% of neurons with profuse axonal branching inside the nucleus and a dendritic arbor that differed from that of STN neurons without local axon collaterals. They had intrinsic electrophysiological properties and in particular, the ability to generate plateau potentials, similar to that of STN neurons without local axon collaterals and more generally to that of classically described STN neurons. This suggests that a subpopulation of STN neurons forms a local glutamatergic network, which together with plateau potentials, allow amplification of hyperdirect cortical inputs and synchronization of the STN neuronal population.
The combination of inducible genetic fate mapping techniques and in vitro targeted patch‐clamp recordings demonstrated the existence of a new type of mouse subthalamic nucleus (STN) neuron that possesses a highly local collateralized axon. These neurons represent twenty percent of fate mapped E11.5–12.5 STN neurons, exhibit different dendritic arbors compared to non‐collateralized STN neurons and have electrophysiological properties similar to that of the general STN population. They are well‐suited to participate to a feed forward excitatory network in the STN.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28971478</pmid><doi>10.1002/cne.24334</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5545-059X</orcidid><orcidid>https://orcid.org/0000-0002-9778-8716</orcidid><orcidid>https://orcid.org/0000-0003-2111-6638</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Axon collaterals basal ganglia calcium binding proteins Cell fate Cortex Electrical stimuli Fate maps Gene mapping Glutamatergic transmission inducible genetic fate mapping Life Sciences Neurons Neurons and Cognition patch‐clamp Placebo effect Rodents RRID: AB_10000340 RRID: AB_10000342 RRID: AB_2313584 RRID: AB_2336933 RRID: AB_2337249 RRID: AB_2650496 Solitary tract nucleus Subthalamic nucleus Synchronization |
title | Mouse subthalamic nucleus neurons with local axon collaterals |
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