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Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
Cindy Orvain, … , Yves Lévy, Sophie Hüe
Cindy Orvain, … , Yves Lévy, Sophie Hüe
Published April 2, 2020
Citation Information: J Clin Invest. 2020;130(7):3777-3790. https://doi.org/10.1172/JCI131180.
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Research Article Dermatology Immunology

Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa

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Abstract

Hidradenitis suppurativa (HS) is a chronic, relapsing, inflammatory skin disease. HS appears to be a primary abnormality in the pilosebaceous-apocrine unit. In this work, we characterized hair follicle stem cells (HFSCs) isolated from HS patients and more precisely the outer root sheath cells (ORSCs). We showed that hair follicle cells from HS patients had an increased number of proliferating progenitor cells and lost quiescent stem cells. Remarkably, we also showed that the progression of replication forks was altered in ORSCs from hair follicles of HS patients, leading to activation of the ATR/CHK1 pathway. These alterations were associated with an increased number of micronuclei and with the presence of cytoplasmic ssDNA, leading to the activation of the IFI16/STING pathway and the production of type I IFNs. This mechanistic analysis of the etiology of HS in the HFSC compartment establishes a formal link between genetic predisposition and skin inflammation observed in HS.

Authors

Cindy Orvain, Yea-Lih Lin, Francette Jean-Louis, Hakim Hocini, Barbara Hersant, Yamina Bennasser, Nicolas Ortonne, Claire Hotz, Pierre Wolkenstein, Michele Boniotto, Pascaline Tisserand, Cécile Lefebvre, Jean-Daniel Lelièvre, Monsef Benkirane, Philippe Pasero, Yves Lévy, Sophie Hüe

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Figure 4

HFSCs from HS patients lacked the quiescent bulge stem cell population.

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HFSCs from HS patients lacked the quiescent bulge stem cell population.
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(A) Representative data from FACS analyses of freshly isolated total hair follicle cells from the HD group. After gating out CD45+ cells and CD117+ cells, freshly isolated total hair follicle cells were divided into 3 populations, including (a) the bulge cells defined as CD200+CD34–, (b) the upper sub-bulge as CD200+CD34+ cells, and (c) the sub-bulge as CD200–CD34+ cells. Each population was divided into CytoK15hiCD49fhi and CytoK15loCD49flo subsets (red and blue populations, respectively); a histogram demonstrates Ki67 staining in each subpopulation. (B) Representative data from FACS analyses of freshly isolated total hair follicle cells from HS patients. (C) Proportion of each subpopulation in freshly isolated total hair follicle–derived epithelial cells of HS patients (n = 19) and HD group (n = 6). (D) Proportion of CytoK15hiCD49fhi subset in CD200+CD34– cells of HS patients (n = 19) and HD group (n = 6) (HS: first quartile 0.58%; third quartile 3.14%; minimum 0.09%; maximum 9.01% vs. HD: first quartile 1.88%; third quartile 13.41%; minimum 1.2%; maximum 15%). Horizontal lines represent the mean ± SD. *P < 0.05 by Mann-Whitney U test.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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