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Jandke, A.* ; Melandri, D.* ; Monin, L.* ; Ushakov, D.S.* ; Laing, A.G.* ; Vantourout, P.* ; East, P.* ; Nitta, T.* ; Narita, T.* ; Takayanagi, H.* ; Feederle, R. ; Hayday, A.*

Butyrophilin-like proteins display combinatorial diversity in selecting and maintaining signature intraepithelial γδ T cell compartments.

Nat. Commun. 11:3769 (2020)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Butyrophilin-like (Btnl) genes are emerging as major epithelial determinants of tissueassociated gamma delta T cell compartments. Thus, the development of signature, murine TCR gamma delta(+) intraepithelial lymphocytes (IEL) in gut and skin depends on Btnl family members, Btnl1 and Skint1, respectively. In seeking mechanisms underlying these profound effects, we now show that normal gut and skin gamma delta IEL development additionally requires Btnl6 and Skint2, respectively, and furthermore that different Btnl heteromers can seemingly shape different intestinal gamma delta(+) IEL repertoires. This formal genetic evidence for the importance of Btnl heteromers also applied to the steady-state, since sustained Btnl expression is required to maintain the signature TCR.V gamma 7(+) IEL phenotype, including specific responsiveness to Btnl proteins. In sum, Btnl proteins are required to select and to maintain the phenotypes of tissue-protective gamma delta IEL compartments, with combinatorially diverse heteromers having differential impacts on different IEL subsets.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Lymphocytes; Homeostasis; Migration; Receptor; Il-15; Site; Tcr; Surveillance; Activation; Expression
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 11, Heft: 1, Seiten: , Artikelnummer: 3769 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) CF Monoclonal Antibodies (CF-MAB)
POF Topic(s) 30201 - Metabolic Health
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502210-001
Förderungen Guy's and St. Thomas' Charity Prize PhD program in Biomedical and Translational Science
King's Bioscience Institute
European Union (EU)
Scopus ID 85088655442
PubMed ID 32724083
Erfassungsdatum 2020-10-07