Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
26 10 2023
Historique:
received: 14 03 2023
accepted: 05 10 2023
medline: 30 10 2023
pubmed: 27 10 2023
entrez: 26 10 2023
Statut: epublish

Résumé

Axon initial segment (AIS) cell surface proteins mediate key biological processes in neurons including action potential initiation and axo-axonic synapse formation. However, few AIS cell surface proteins have been identified. Here, we use antibody-directed proximity biotinylation to define the cell surface proteins in close proximity to the AIS cell adhesion molecule Neurofascin. To determine the distributions of the identified proteins, we use CRISPR-mediated genome editing for insertion of epitope tags in the endogenous proteins. We identify Contactin-1 (Cntn1) as an AIS cell surface protein. Cntn1 is enriched at the AIS through interactions with Neurofascin and NrCAM. We further show that Cntn1 contributes to assembly of the AIS extracellular matrix, and regulates AIS axo-axonic innervation by inhibitory basket cells in the cerebellum and inhibitory chandelier cells in the cortex.

Identifiants

pubmed: 37884508
doi: 10.1038/s41467-023-42273-8
pii: 10.1038/s41467-023-42273-8
pmc: PMC10603070
doi:

Substances chimiques

Contactin 1 0
Membrane Proteins 0
Antibodies 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6797

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS116897
Pays : United States
Organisme : NINDS NIH HHS
ID : R35 NS122073
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH119819
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© 2023. The Author(s).

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Auteurs

Yuki Ogawa (Y)

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Brian C Lim (BC)

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Shanu George (S)

Division of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

Juan A Oses-Prieto (JA)

Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.

Joshua M Rasband (JM)

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Yael Eshed-Eisenbach (Y)

Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

Hamdan Hamdan (H)

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.
Department of Physiology and Immunology, Khalifa University, Abu Dhabi, United Arab Emirates.

Supna Nair (S)

Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.

Francesco Boato (F)

Division of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

Elior Peles (E)

Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

Alma L Burlingame (AL)

Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.

Linda Van Aelst (L)

Division of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

Matthew N Rasband (MN)

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA. rasband@bcm.edu.

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Classifications MeSH