GABAergic striatal neurons project dendrites and axons into the postnatal subventricular zone leading to calcium activity
Identifieur interne : 001317 ( Ncbi/Curation ); précédent : 001316; suivant : 001318GABAergic striatal neurons project dendrites and axons into the postnatal subventricular zone leading to calcium activity
Auteurs : Stephanie Z. Young [États-Unis] ; Carlos A. Lafourcade [États-Unis] ; Jean-Claude Platel [France] ; Tiffany V. Lin [États-Unis] ; Angélique Bordey [États-Unis]Source :
- Frontiers in Cellular Neuroscience [ 1662-5102 ] ; 2014.
Abstract
GABA regulates the behavior of neuroblasts and neural progenitor cells in the postnatal neurogenic subventricular zone (SVZ) through GABAA receptor (GABAAR)-mediated calcium increases. However, the source of GABA necessary for sufficient GABAAR-mediated depolarization and calcium increase has remained speculative. Here, we explored whether GABAergic striatal neurons functionally connect with SVZ cells. Using patch clamp recordings or single cell electroporation, striatal neurons along the SVZ were filled with a fluorescent dye revealing that they send both dendrites and axons into the SVZ. About 93% of the recorded neurons were medium spiny or aspiny GABAergic neurons and each neuron sent 3–4 processes into the SVZ covering ~56 μm. Using calcium imaging, we found that depolarization of striatal neurons led to increased calcium activity in SVZ cells that were mediated by GABAAR activation. Collectively, these findings undercover a novel mode of signaling in the SVZ providing a mechanism of brain activity-mediated regulation of postnatal neurogenesis through GABAergic striatal activity.
Url:
DOI: 10.3389/fncel.2014.00010
PubMed: 24478632
PubMed Central: 3904109
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Young</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Departments of Neurosurgery and Cellular and Molecular Physiology, Yale University School of Medicine</institution><country>New Haven, CT, USA</country></nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Lafourcade, Carlos A" sort="Lafourcade, Carlos A" uniqKey="Lafourcade C" first="Carlos A." last="Lafourcade">Carlos A. Lafourcade</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Departments of Neurosurgery and Cellular and Molecular Physiology, Yale University School of Medicine</institution><country>New Haven, CT, USA</country></nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Platel, Jean Claude" sort="Platel, Jean Claude" uniqKey="Platel J" first="Jean-Claude" last="Platel">Jean-Claude Platel</name><affiliation wicri:level="1"><nlm:aff id="aff2"><institution>Developmental Biology, Aix-Marseille University, IBDML, CNRS, UMR7288</institution><country>Marseille, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Lin, Tiffany V" sort="Lin, Tiffany V" uniqKey="Lin T" first="Tiffany V." last="Lin">Tiffany V. Lin</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Departments of Neurosurgery and Cellular and Molecular Physiology, Yale University School of Medicine</institution><country>New Haven, CT, USA</country></nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea></wicri:regionArea></affiliation></author><author><name sortKey="Bordey, Angelique" sort="Bordey, Angelique" uniqKey="Bordey A" first="Angélique" last="Bordey">Angélique Bordey</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Departments of Neurosurgery and Cellular and Molecular Physiology, Yale University School of Medicine</institution><country>New Haven, CT, USA</country></nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea></wicri:regionArea></affiliation></author></analytic><series><title level="j">Frontiers in Cellular Neuroscience</title><idno type="eISSN">1662-5102</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>GABA regulates the behavior of neuroblasts and neural progenitor cells in the postnatal neurogenic subventricular zone (SVZ) through GABA<sub>A</sub> receptor (GABA<sub>A</sub>R)-mediated calcium increases. However, the source of GABA necessary for sufficient GABA<sub>A</sub>R-mediated depolarization and calcium increase has remained speculative. Here, we explored whether GABAergic striatal neurons functionally connect with SVZ cells. Using patch clamp recordings or single cell electroporation, striatal neurons along the SVZ were filled with a fluorescent dye revealing that they send both dendrites and axons into the SVZ. About 93% of the recorded neurons were medium spiny or aspiny GABAergic neurons and each neuron sent 3–4 processes into the SVZ covering ~56 μm. Using calcium imaging, we found that depolarization of striatal neurons led to increased calcium activity in SVZ cells that were mediated by GABA<sub>A</sub>R activation. 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