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Empl, L.* ; Chovsepian, A.* ; Chahin, M.* ; Kan, W.Y.V.* ; Fourneau, J.* ; Van Steenbergen, V.* ; Weidinger, S.* ; Marcantoni, M.* ; Ghanem, A.* ; Bradley, P.* ; Conzelmann, K.K.* ; Cai, R. ; Ghasemigharagoz, A. ; Ertürk, A. ; Wagner, I.* ; Kreutzfeldt, M.* ; Merkler, D.* ; Liebscher, S.* ; Bareyre, F.M.*

Selective plasticity of callosal neurons in the adult contralesional cortex following murine traumatic brain injury.

Nat. Commun. 13:2659 (2022)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Traumatic brain injury (TBI) results in deficits that are often followed by recovery. The contralesional cortex can contribute to this process but how distinct contralesional neurons and circuits respond to injury remains to be determined. To unravel adaptations in the contralesional cortex, we used chronic in vivo two-photon imaging. We observed a general decrease in spine density with concomitant changes in spine dynamics over time. With retrograde co-labeling techniques, we showed that callosal neurons are uniquely affected by and responsive to TBI. To elucidate circuit connectivity, we used monosynaptic rabies tracing, clearing techniques and histology. We demonstrate that contralesional callosal neurons adapt their input circuitry by strengthening ipsilateral connections from pre-connected areas. Finally, functional in vivo two-photon imaging demonstrates that the restoration of pre-synaptic circuitry parallels the restoration of callosal activity patterns. Taken together our study thus delineates how callosal neurons structurally and functionally adapt following a contralateral murine TBI.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 13, Heft: 1, Seiten: , Artikelnummer: 2659 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Tissue Engineering and Regenerative Medicine (ITERM)
Förderungen Deutsche Forschungsgemeinschaft (German Research Foundation)