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1000 Titel
  • Brain extracellular matrix retains connectivity in neuronal networks
1000 Autor/in
  1. Bikbaev, Arthur |
  2. Frischknecht, Renato |
  3. Heine, Martin |
1000 Erscheinungsjahr 2015
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2015-09-29
1000 Erschienen in
1000 Quellenangabe
  • 5: 14527
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2015
1000 Lizenz
1000 Verlagsversion
  • https://dx.doi.org/10.1038/srep14527 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586818/ |
1000 Ergänzendes Material
  • https://www.nature.com/articles/srep14527#supplementary-information |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The formation and maintenance of connectivity are critically important for the processing and storage of information in neuronal networks. The brain extracellular matrix (ECM) appears during postnatal development and surrounds most neurons in the adult mammalian brain. Importantly, the removal of the ECM was shown to improve plasticity and post-traumatic recovery in the CNS, but little is known about the mechanisms. Here, we investigated the role of the ECM in the regulation of the network activity in dissociated hippocampal cultures grown on microelectrode arrays (MEAs). We found that enzymatic removal of the ECM in mature cultures led to transient enhancement of neuronal activity, but prevented disinhibition-induced hyperexcitability that was evident in age-matched control cultures with intact ECM. Furthermore, the ECM degradation followed by disinhibition strongly affected the network interaction so that it strongly resembled the juvenile pattern seen in naïve developing cultures. Taken together, our results demonstrate that the ECM plays an important role in retention of existing connectivity in mature neuronal networks that can be exerted through synaptic confinement of glutamate. On the other hand, removal of the ECM can play a permissive role in modification of connectivity and adaptive exploration of novel network architecture.
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/QmlrYmFldiwgQXJ0aHVy|https://frl.publisso.de/adhoc/creator/RnJpc2Noa25lY2h0LMKgUmVuYXRv|https://frl.publisso.de/adhoc/creator/SGVpbmUsIE1hcnRpbg==
1000 Label
1000 Förderer
  1. Federal State of Saxony-Anhalt |
  2. ERA-net NEURON |
  3. Deutsche Forschungsgemeinschaft (DFG) |
  4. Schram Foundation |
1000 Fördernummer
  1. -
  2. -
  3. HE-3604/2-1
  4. T287/21796/2011
1000 Förderprogramm
  1. LSA RG Molecular Physiology
  2. Moddifsyn
  3. -
  4. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Federal State of Saxony-Anhalt |
    1000 Förderprogramm LSA RG Molecular Physiology
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer ERA-net NEURON |
    1000 Förderprogramm Moddifsyn
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Deutsche Forschungsgemeinschaft (DFG) |
    1000 Förderprogramm -
    1000 Fördernummer HE-3604/2-1
  4. 1000 joinedFunding-child
    1000 Förderer Schram Foundation |
    1000 Förderprogramm -
    1000 Fördernummer T287/21796/2011
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6404867.rdf
1000 Erstellt am 2017-10-05T19:02:25.782+0200
1000 Erstellt von 218
1000 beschreibt frl:6404867
1000 Bearbeitet von 218
1000 Zuletzt bearbeitet Thu Aug 05 14:00:20 CEST 2021
1000 Objekt bearb. Thu Aug 05 14:00:19 CEST 2021
1000 Vgl. frl:6404867
1000 Oai Id
  1. oai:frl.publisso.de:frl:6404867 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

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