TY - JOUR
T1 - Identification of phenotypically and functionally heterogeneous mouse mucosal-associated invariant T cells using MR1 tetramers
AU - Rahimpour, Azad
AU - Koay, Hui Fern
AU - Enders, Anselm
AU - Clanchy, Rhiannon
AU - Eckle, Sidonia B.G.
AU - Meehan, Bronwyn
AU - Chen, Zhenjun
AU - Whittle, Belinda
AU - Liu, Ligong
AU - Fairlie, David P.
AU - Goodnow, Chris C.
AU - McCluskey, James
AU - Rossjohn, Jamie
AU - Uldrich, Adam P.
AU - Pellicci, Daniel G.
AU - Godfrey, Dale I.
N1 - Publisher Copyright:
© 2015 Rahimpour et al.
PY - 2015/6/29
Y1 - 2015/6/29
N2 - Studies on the biology of mucosal-associated invariant T cells (MAIT cells) in mice have been hampered by a lack of specific reagents. Using MR1-antigen (Ag) tetramers that specifically bind to the MR1-restricted MAIT T cell receptors (TCRs), we demonstrate that MAIT cells are detectable in a broad range of tissues in C57BL/6 and BALB/c mice. These cells include CD4-CD8-, CD4-CD8+, and CD4+CD8- subsets, and their frequency varies in a tissue- and strain-specific manner. Mouse MAIT cells have a CD44hiCD62Llo memory phenotype and produce high levels of IL-17A, whereas other cytokines, including IFN-γ, IL-4, IL-10, IL-13, and GM-CSF, are produced at low to moderate levels. Consistent with high IL-17A production, most MAIT cells express high levels of retinoic acid-related orphan receptor γt (RORγt), whereas RORγtlo MAIT cells predominantly express T-bet and produce IFN-γ. Most MAIT cells express the promyelocytic leukemia zinc finger (PLZF) transcription factor, and their development is largely PLZF dependent. These observations contrast with previous reports that MAIT cells from Vα19 TCR transgenic mice are PLZF- and express a naive CD44lo phenotype. Accordingly, MAIT cells from normal mice more closely resemble human MAIT cells than previously appreciated, and this provides the foundation for further investigations of these cells in health and disease.
AB - Studies on the biology of mucosal-associated invariant T cells (MAIT cells) in mice have been hampered by a lack of specific reagents. Using MR1-antigen (Ag) tetramers that specifically bind to the MR1-restricted MAIT T cell receptors (TCRs), we demonstrate that MAIT cells are detectable in a broad range of tissues in C57BL/6 and BALB/c mice. These cells include CD4-CD8-, CD4-CD8+, and CD4+CD8- subsets, and their frequency varies in a tissue- and strain-specific manner. Mouse MAIT cells have a CD44hiCD62Llo memory phenotype and produce high levels of IL-17A, whereas other cytokines, including IFN-γ, IL-4, IL-10, IL-13, and GM-CSF, are produced at low to moderate levels. Consistent with high IL-17A production, most MAIT cells express high levels of retinoic acid-related orphan receptor γt (RORγt), whereas RORγtlo MAIT cells predominantly express T-bet and produce IFN-γ. Most MAIT cells express the promyelocytic leukemia zinc finger (PLZF) transcription factor, and their development is largely PLZF dependent. These observations contrast with previous reports that MAIT cells from Vα19 TCR transgenic mice are PLZF- and express a naive CD44lo phenotype. Accordingly, MAIT cells from normal mice more closely resemble human MAIT cells than previously appreciated, and this provides the foundation for further investigations of these cells in health and disease.
UR - http://www.scopus.com/inward/record.url?scp=84944872887&partnerID=8YFLogxK
U2 - 10.1084/jem.20142110
DO - 10.1084/jem.20142110
M3 - Article
SN - 0022-1007
VL - 212
SP - 1095
EP - 1108
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 7
ER -