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Regulatory T Cells in Skin Facilitate Epithelial Stem Cell Differentiation
Author(s) -
Niwa Ali,
Bahar Zirak,
Robert Sanchez Rodriguez,
Mariela Pauli,
Hong-An Truong,
Kevin Lai,
Richard Ahn,
Kaitlin Corbin,
Margaret M. Lowe,
Tiffany C. Scharschmidt,
Keyon Taravati,
Madeleine R. Tan,
Roberto R. Ricardo-González,
Audrey Nosbaum,
Marta Bertolini,
Wilson Liao,
Frank O. Nestlé,
Ralf Paus,
George Cotsarelis,
Abul K. Abbas,
Michael D. Rosenblum
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.05.002
Subject(s) - biology , microbiology and biotechnology , stem cell , immune system , regeneration (biology) , cellular differentiation , notch signaling pathway , function (biology) , immunology , signal transduction , gene , genetics
The maintenance of tissue homeostasis is critically dependent on the function of tissue-resident immune cells and the differentiation capacity of tissue-resident stem cells (SCs). How immune cells influence the function of SCs is largely unknown. Regulatory T cells (Tregs) in skin preferentially localize to hair follicles (HFs), which house a major subset of skin SCs (HFSCs). Here, we mechanistically dissect the role of Tregs in HF and HFSC biology. Lineage-specific cell depletion revealed that Tregs promote HF regeneration by augmenting HFSC proliferation and differentiation. Transcriptional and phenotypic profiling of T regs and HFSCs revealed that skin-resident Tregs preferentially express high levels of the Notch ligand family member, Jagged 1 (Jag1). Expression of Jag1 on Tregs facilitated HFSC function and efficient HF regeneration. Taken together, our work demonstrates that Tregs in skin play a major role in HF biology by promoting the function of HFSCs.

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