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1000 Titel
  • Disruption of Kcc2-dependent inhibition of olfactory bulb output neurons suggests its importance in odour discrimination
1000 Autor/in
  1. Gödde, Kathrin |
  2. Gschwend, Olivier |
  3. Puchkov, Dmytro |
  4. Pfeffer, Carsten K. |
  5. Carleton, Alan |
  6. Jentsch, Thomas |
1000 Erscheinungsjahr 2016
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2016-07-08
1000 Erschienen in
1000 Quellenangabe
  • 7:12043
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2016
1000 Lizenz
1000 Verlagsversion
  • http://dx.doi.org/10.1038/ncomms12043 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941119/ |
1000 Ergänzendes Material
  • https://www.nature.com/articles/ncomms12043#supplementary-information |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Synaptic inhibition in the olfactory bulb (OB), the first relay station of olfactory information, is believed to be important for odour discrimination. We interfered with GABAergic inhibition of mitral and tufted cells (M/T cells), the principal neurons of the OB, by disrupting their potassium-chloride cotransporter 2 (Kcc2). Roughly, 70% of mice died around 3 weeks, but surviving mice appeared normal. In these mice, the resulting increase in the intracellular Cl− concentration nearly abolished GABA-induced hyperpolarization of mitral cells (MCs) and unexpectedly increased the number of perisomatic synapses on MCs. In vivo analysis of odorant-induced OB electrical activity revealed increased M/T cell firing rate, altered phasing of action potentials in the breath cycle and disrupted separation of odour-induced M/T cell activity patterns. Mice also demonstrated a severely impaired ability to discriminate chemically similar odorants or odorant mixtures. Our work suggests that precisely tuned GABAergic inhibition onto M/T cells is crucial for M/T cell spike pattern separation needed to distinguish closely similar odours.
1000 Sacherschließung
lokal Sensory processing
lokal Olfactory bulb
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/R8O2ZGRlLCBLYXRocmlu|https://frl.publisso.de/adhoc/creator/R3NjaHdlbmQsIE9saXZpZXI=|http://orcid.org/0000-0001-8341-4847|https://frl.publisso.de/adhoc/creator/UGZlZmZlciwgQ2Fyc3RlbiBLLg==|https://frl.publisso.de/adhoc/creator/Q2FybGV0b24sIEFsYW4=|http://orcid.org/0000-0002-3509-2553
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft (DFG) |
  2. University of Geneva |
  3. European Research Council |
  4. Swiss National Science Foundation |
  5. Boehringer Ingelheim Fonds |
1000 Fördernummer
  1. JE 164/8; Exc 257
  2. -
  3. ERC-2009-StG-243344-NEUROCHEMS
  4. 31003A_153410
  5. -
1000 Förderprogramm
  1. NeuroCure
  2. -
  3. -
  4. -
  5. PhD fellowship
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Deutsche Forschungsgemeinschaft (DFG) |
    1000 Förderprogramm NeuroCure
    1000 Fördernummer JE 164/8; Exc 257
  2. 1000 joinedFunding-child
    1000 Förderer University of Geneva |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer European Research Council |
    1000 Förderprogramm -
    1000 Fördernummer ERC-2009-StG-243344-NEUROCHEMS
  4. 1000 joinedFunding-child
    1000 Förderer Swiss National Science Foundation |
    1000 Förderprogramm -
    1000 Fördernummer 31003A_153410
  5. 1000 joinedFunding-child
    1000 Förderer Boehringer Ingelheim Fonds |
    1000 Förderprogramm PhD fellowship
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6403751.rdf
1000 Erstellt am 2017-08-09T12:25:40.791+0200
1000 Erstellt von 122
1000 beschreibt frl:6403751
1000 Bearbeitet von 288
1000 Zuletzt bearbeitet 2022-08-18T07:54:43.298+0200
1000 Objekt bearb. Wed Jan 27 11:44:34 CET 2021
1000 Vgl. frl:6403751
1000 Oai Id
  1. oai:frl.publisso.de:frl:6403751 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
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