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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 6

Expression of Hippo pathway genes and their association with HS FB pseudotime.

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Expression of Hippo pathway genes and their association with HS FB pseud...
(A and B) Percentage of FB subtypes expressing Hippo pathway marker (A) and target genes (B). (C) IHC showing localization of Hippo pathway marker genes (patient HS1). Scale bars: top, 6 mm; bottom, 200 μm. (D and E) Scatterplots showing the activation z scores of Hippo pathway marker genes (D) and activated cytokine and growth factor upstream regulators (E) as upstream regulators for the SFRP4+ and CXCL13+ FBs. (F) Pseudotime trajectory of HS SFRP2+, SFRP4+, and CXCL13+ FBs colored by the pseudotime. Dark blue represents early, light blue represents late pseudotime. (G) Pseudotime trajectory colored by the pseudotime subcluster of the FBs. (H) Pseudotime trajectory colored by the subtype identity of HS FBs. (I and J) Scatterplots showing the correlation between the FB pseudotimes and module scores for previously identified upstream regulators (I) and Hippo pathway–associated genes (J). The color represents the pseudotime subcluster identity of the cell.

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

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