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)
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.
Impact Factor
Scopus SNIP
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Times Cited
Scopus
Cited By
Altmetric
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Typ der Hochschulschrift
Herausgeber
Schlagwörter
Lymphocytes; Homeostasis; Migration; Receptor; Il-15; Site; Tcr; Surveillance; Activation; Expression
Keywords plus
Sprache
englisch
Veröffentlichungsjahr
2020
Prepublished im Jahr
HGF-Berichtsjahr
2020
ISSN (print) / ISBN
2041-1723
e-ISSN
2041-1723
ISBN
Bandtitel
Konferenztitel
Konferzenzdatum
Konferenzort
Konferenzband
Quellenangaben
Band: 11,
Heft: 1,
Seiten: ,
Artikelnummer: 3769
Supplement: ,
Reihe
Verlag
Nature Publishing Group
Verlagsort
London
Tag d. mündl. Prüfung
0000-00-00
Betreuer
Gutachter
Prüfer
Topic
Hochschule
Hochschulort
Fakultät
Veröffentlichungsdatum
0000-00-00
Anmeldedatum
0000-00-00
Anmelder/Inhaber
weitere Inhaber
Anmeldeland
Priorität
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)
Copyright
Erfassungsdatum
2020-10-07