A monoclonal Trd chain supports the development of the complete set of functional γδ T cell lineages.


Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
28 03 2023
Historique:
received: 23 06 2022
revised: 14 11 2022
accepted: 28 02 2023
medline: 3 4 2023
pubmed: 16 3 2023
entrez: 15 3 2023
Statut: ppublish

Résumé

The clonal selection theory describes key features of adaptive immune responses of B and T cells. For αβ T cells and B cells, antigen recognition and selection principles are known at a detailed molecular level. The precise role of the antigen receptor in γδ T cells remains less well understood. To better understand the role of the γδ T cell receptor (TCR), we generate an orthotopic TCRδ transgenic mouse model. We demonstrate a multi-layered functionality of γδ TCRs and diverse roles of CDR3δ-mediated selection during γδ T cell development. Whereas epithelial populations using Vγ5 or Vγ7 chains are almost unaffected in their biology in the presence of the transgenic TCRδ chain, pairing with Vγ1 positively selects γδ T cell subpopulations with distinct programs in several organs, thereby distorting the repertoire. In conclusion, our data support dictation of developmental tropism together with adaptive-like recognition principles in a single antigen receptor.

Identifiants

pubmed: 36920908
pii: S2211-1247(23)00264-4
doi: 10.1016/j.celrep.2023.112253
pii:
doi:

Substances chimiques

Receptors, Antigen, T-Cell, gamma-delta 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

112253

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Anne M Hahn (AM)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Lisa Vogg (L)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Stefanie Brey (S)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Andrea Schneider (A)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Simon Schäfer (S)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Ralph Palmisano (R)

Optical Imaging Centre Erlangen (OICE), Competence Unit, FAU, 91058 Erlangen, Germany.

Anna Pavlova (A)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Inga Sandrock (I)

Medizinische Hochschule Hannover, Hannover, Germany.

Likai Tan (L)

Medizinische Hochschule Hannover, Hannover, Germany.

Alina S Fichtner (AS)

Medizinische Hochschule Hannover, Hannover, Germany.

Immo Prinz (I)

Medizinische Hochschule Hannover, Hannover, Germany; Institute for Systems Immunology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Sarina Ravens (S)

Medizinische Hochschule Hannover, Hannover, Germany.

Thomas H Winkler (TH)

Division of Genetics, Department Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany. Electronic address: thomas.winkler@fau.de.

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Classifications MeSH