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Single-cell sequencing reveals Hippo signaling as a driver of fibrosis in hidradenitis suppurativa
Kelsey R. van Straalen, … , Lam C. Tsoi, Johann E. Gudjonsson
Kelsey R. van Straalen, … , Lam C. Tsoi, Johann E. Gudjonsson
Published December 5, 2023
Citation Information: J Clin Invest. 2024;134(3):e169225. https://doi.org/10.1172/JCI169225.
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Research Article Dermatology Inflammation

Single-cell sequencing reveals Hippo signaling as a driver of fibrosis in hidradenitis suppurativa

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Abstract

Hidradenitis suppurativa (HS) is a chronic inflammatory disease characterized by abscesses, nodules, dissecting/draining tunnels, and extensive fibrosis. Here, we integrate single-cell RNA sequencing, spatial transcriptomics, and immunostaining to provide an unprecedented view of the pathogenesis of chronic HS, characterizing the main cellular players and defining their interactions. We found a striking layering of the chronic HS infiltrate and identified the contribution of 2 fibroblast subtypes (SFRP4+ and CXCL13+) in orchestrating this compartmentalized immune response. We further demonstrated the central role of the Hippo pathway in promoting extensive fibrosis in HS and provided preclinical evidence that the profibrotic fibroblast response in HS can be modulated through inhibition of this pathway. These data provide insights into key aspects of HS pathogenesis with broad therapeutic implications.

Authors

Kelsey R. van Straalen, Feiyang Ma, Pei-Suen Tsou, Olesya Plazyo, Mehrnaz Gharaee-Kermani, Marta Calbet, Xianying Xing, Mrinal K. Sarkar, Ranjitha Uppala, Paul W. Harms, Rachael Wasikowski, Lina Nahlawi, Mio Nakamura, Milad Eshaq, Cong Wang, Craig Dobry, Jeffrey H. Kozlow, Jill Cherry-Bukowiec, William D. Brodie, Kerstin Wolk, Özge Uluçkan, Megan N. Mattichak, Matteo Pellegrini, Robert L. Modlin, Emanual Maverakis, Robert Sabat, J. Michelle Kahlenberg, Allison C. Billi, Lam C. Tsoi, Johann E. Gudjonsson

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Figure 3

Identification of myeloid cell and T cell subsets in HS lesional skin.

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Identification of myeloid cell and T cell subsets in HS lesional skin.
(...
(A) UMAP showing 689 myeloid cells colored by subtype. (B) UMAP showing the cells colored by disease condition. (C) Bar chart showing the subtypes as percentage component of disease. (D) Dot plot showing representative marker genes for each subtype. Color represents scaled expression; size of the dot represents the percentage of cells expressing the gene. (E) IHC showing myeloid cell subtype localization in HS lesional skin (patient HS1). Scale bars: top, 6 mm; bottom, 200 μm. (F–H) Bar chart showing enriched Gene Ontology biological processes in HS cDC2B cells (F), macrophages (G), and pDCs (H). Green, immune associated; blue, transcription related and other biological processes. (I) UMAP showing 3,985 T cells colored by subtype. (J) UMAP showing T cells colored by disease condition. (K) Bar chart showing the T cell subtypes as percentage component of disease. (L) Dot plot showing representative marker genes for T cell subtypes. Color represents scaled expression; size of the dot represents the percentage of cells expressing the gene. (M and N) Scatterplots showing the correlation between the levels of expression of IL-17A (x axis) and CD4 (M, ρ = 0.03) or CD8A (N, ρ = 0.01). (O) Scatterplot showing the correlation between the levels of expression of IL-17A and IL-17F, ρ = 0.44, among T cells.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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