Hepatocyte Growth Factor has Unique Functions in Keratinocytes that differs from IL-17A and TNF and may contribute to Inflammatory Pathways in Hidradenitis Suppurativa.

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Journal

The Journal of investigative dermatology
ISSN: 1523-1747
Titre abrégé: J Invest Dermatol
Pays: United States
ID NLM: 0426720

Informations de publication

Date de publication:
20 Jul 2024
Historique:
received: 05 04 2024
revised: 19 06 2024
accepted: 02 07 2024
medline: 23 7 2024
pubmed: 23 7 2024
entrez: 22 7 2024
Statut: aheadofprint

Résumé

Hidradenitis suppurativa (HS) is a chronic inflammatory disease that is difficult to control, and its mechanism remains unclear. Hepatocyte growth factor (HGF) has been reported to be significantly upregulated in the serum and skin of HS patients, especially in the lesions with tunnels. In this study, we examined the transcriptome of HGF-treated keratinocytes (KCs) and compared it with genetic profiling of HS lesions. HGF was highly expressed in HS skin, especially in the deep dermis, compared to healthy controls, and its source was mainly fibroblasts. HGF upregulated more genes in KCs than interleukin-17A or tumor necrosis factor-α, and these genes included multiple epithelial-mesenchymal transition (EMT)-related genes. Differentially expressed genes in HGF-stimulated KCs were involved in activation of EMT-related pathways. These HGF-induced genes were significantly upregulated in HS lesions compared to healthy skin and non-lesions and were more strongly associated with HS tunnels. In summary, HGF was highly expressed in HS and induced EMT-related genes in KCs; HGF-induced genes were highly associated with gene profiling of HS with tunnels, suggesting that HGF may be involved in HS tunnel formation via EMT.

Identifiants

pubmed: 39038532
pii: S0022-202X(24)01918-3
doi: 10.1016/j.jid.2024.07.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Naomi Shishido-Takahashi (N)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA; Department of Dermatology, The University of Tokyo, Tokyo, Japan.

Sandra Garcet (S)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA.

Inna Cueto (I)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA.

Shunsuke Miura (S)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA; Department of Dermatology, The University of Tokyo, Tokyo, Japan.

Xuan Li (X)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA.

Darshna Rambhia (D)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA.

Norma Kunjravia (N)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA.

Hong Beom Hur (HB)

Research Bioinformatics, Center for Clinical and Translational Science, The Rockefeller University, New York, NY, USA.

Young In Lee (YI)

Department of Dermatology & Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Seoyoon Ham (S)

Department of Dermatology & Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Nabeeha Anis (N)

West Windsor-Plainsboro High School South, West Windsor, NJ, USA.

Jaehwan Kim (J)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA; Department of Dermatology, University of California, Davis, Sacramento, CA, USA.

James G Krueger (JG)

Laboratory of Investigative Dermatology, The Rockefeller University, New York, NY, USA. Electronic address: kruegej@rockefeller.edu.

Classifications MeSH