Treg-Cell Control of a CXCL5-IL-17 Inflammatory Axis Promotes Hair-Follicle-Stem-Cell Differentiation During Skin-Barrier Repair

被引：132

作者：

Mathur, Anubhav N. ^{[1
]}

Zirak, Bahar ^{[1
]}

Boothby, Ian C. ^{[1
]}

Tan, Madge ^{[1
]}

Cohen, Jarish N. ^{[1
]}

Mauro, Thea M. ^{[1
]}

Mehta, Pooja ^{[1
]}

Lowe, Margaret M. ^{[1
]}

Abbas, Abul K. ^{[2
]}

Ali, Niwa ^{[1
]}

Rosenblum, Michael D. ^{[1
]}

机构：

[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA

[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA

来源：

IMMUNITY | 2019年 / 50卷 / 03期

关键词：

REGULATORY T-CELLS; IMMUNE DYSREGULATION; NICHE; POLYENDOCRINOPATHY; ENTEROPATHY; CXCL5; MAINTENANCE; RECRUITMENT; HOMEOSTASIS; CONTRIBUTE;

D O I：

10.1016/j.immuni.2019.02.013

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

071005 [微生物学]; 100108 [医学免疫学];

摘要：

Restoration of barrier-tissue integrity after injury is dependent on the function of immune cells and stem cells (SCs) residing in the tissue. In response to skin injury, hair-follicle stem cells (HFSCs), normally poised for hair generation, are recruited to the site of injury and differentiate into cells that repair damaged epithelium. We used a SC fate-mapping approach to examine the contribution of regulatory T (Treg) cells to epidermal-barrier repair after injury. Depletion of Treg cells impaired skin-barrier regeneration and was associated with a Th17 inflammatory response and failed HFSC differentiation. In this setting, damaged epithelial cells preferentially expressed the neutrophil chemoattractant CXCL5, and blockade of CXCL5 or neutrophil depletion restored barrier function and SC differentiation after epidermal injury. Thus, Treg-cell regulation of localized inflammation enables HFSC differentiation and, thereby, skin-barrier regeneration, with implications for the maintenance and repair of other barrier tissues.

引用

页码：655 / +

页数：17

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