Reduced WNT4 expression in normal skin fibroblasts leads to 'Dupuytren-like' changes in the transcriptome.


Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 13 12 2023
revised: 13 09 2024
accepted: 16 09 2024
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 9 10 2024
Statut: epublish

Résumé

Dupuytren's disease (DD) is a fibro-proliferative disorder of unknown aetiology. Previous studies have implicated multiple WNT signalling genes/proteins in Dupuytren pathology, including WNT4. However, it is not yet clear whether WNT signalling dysregulation plays an important role in the initiation of the disease or progression. The aim of this study was to determine if loss of WNT4 expression triggered 'Dupuytren-like' changes in the transcriptome of healthy skin fibroblasts. Fibroblasts were isolated from the wrists of healthy adult males and from the wrists and disease cord tissue from males in a family positive for Dupuytren's disease. Normal skin fibroblasts from healthy controls were treated with WNT4 siRNA and scrambled controls. RNASeq was used to analyse the transcriptomes of disease and non-disease fibroblasts from patients with Dupuytren's as well as in siRNA treated and non-treated control fibroblasts. Analysis of the transcriptomes from DD patient and normal skin fibroblasts showed significant differences, including in WNT4 expression. Downregulation of WNT4 in normal skin fibroblasts using siRNA led to 'DD-like' changes in the transcriptome. In people susceptible to DD WNT4 is downregulated even in non-fibrotic fibroblasts. Knockdown of WNT4 in normal fibroblasts led to changes that made cells 'DD-like'. This study shows that WNT4 is down regulated in 'non-disease' cells, and that downregulating WNT4 in normal skin fibroblasts leads to widespread 'DD like' changes in the transcriptome, suggesting WNT4 downregulation is a key driver of DD.

Sections du résumé

Background UNASSIGNED
Dupuytren's disease (DD) is a fibro-proliferative disorder of unknown aetiology. Previous studies have implicated multiple WNT signalling genes/proteins in Dupuytren pathology, including WNT4. However, it is not yet clear whether WNT signalling dysregulation plays an important role in the initiation of the disease or progression. The aim of this study was to determine if loss of WNT4 expression triggered 'Dupuytren-like' changes in the transcriptome of healthy skin fibroblasts.
Methods UNASSIGNED
Fibroblasts were isolated from the wrists of healthy adult males and from the wrists and disease cord tissue from males in a family positive for Dupuytren's disease. Normal skin fibroblasts from healthy controls were treated with WNT4 siRNA and scrambled controls. RNASeq was used to analyse the transcriptomes of disease and non-disease fibroblasts from patients with Dupuytren's as well as in siRNA treated and non-treated control fibroblasts.
Results UNASSIGNED
Analysis of the transcriptomes from DD patient and normal skin fibroblasts showed significant differences, including in WNT4 expression. Downregulation of WNT4 in normal skin fibroblasts using siRNA led to 'DD-like' changes in the transcriptome.
Conclusion UNASSIGNED
In people susceptible to DD WNT4 is downregulated even in non-fibrotic fibroblasts. Knockdown of WNT4 in normal fibroblasts led to changes that made cells 'DD-like'. This study shows that WNT4 is down regulated in 'non-disease' cells, and that downregulating WNT4 in normal skin fibroblasts leads to widespread 'DD like' changes in the transcriptome, suggesting WNT4 downregulation is a key driver of DD.

Identifiants

pubmed: 39381224
doi: 10.1016/j.heliyon.2024.e38016
pii: S2405-8440(24)14047-9
pmc: PMC11458971
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e38016

Informations de copyright

© 2024 The Authors. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Aoife O'Brien (A)

Department of Anatomy and Regenerative Medicine, Royal College of Surgeons, Ireland.
Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Andrew Stevenson (A)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Lucy Barrett (L)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Nicholas B Lawler (NB)

School of Molecular Sciences, The University of Western Australia, Perth, WA, 6009, Australia.

Nicole Hortin (N)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Zhenjun Deng (Z)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Amira Allahham (A)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.

Fabio Quondamatteo (F)

Department of Anatomy and Regenerative Medicine, Royal College of Surgeons, Ireland.

Nicole Smith (N)

School of Molecular Sciences, The University of Western Australia, Perth, WA, 6009, Australia.

K Swaminathan Iyer (KS)

School of Molecular Sciences, The University of Western Australia, Perth, WA, 6009, Australia.

Fiona M Wood (FM)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.
Burns Service of Western Australia, WA Department of Health, Perth, WA, Australia.
Fiona Wood Foundation, Murdoch, WA, Australia.

Mark W Fear (MW)

Burn Injury Research Unit (BIRU), School of Biomedical Sciences, University of Western Australia, Australia.
Fiona Wood Foundation, Murdoch, WA, Australia.

Classifications MeSH