Composition of TWIST1 dimers regulates fibroblast activation and tissue fibrosis
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27113414
DOI
10.1136/annrheumdis-2015-208470
PII: S0003-4967(24)01601-7
Knihovny.cz E-zdroje
- Klíčová slova
- Fibroblasts, Systemic Sclerosis, Treatment,
- MeSH
- fibroblasty účinky léků metabolismus MeSH
- genový knockdown MeSH
- jaderné proteiny biosyntéza nedostatek genetika metabolismus fyziologie MeSH
- kůže patologie MeSH
- lidé MeSH
- malá interferující RNA genetika MeSH
- messenger RNA genetika MeSH
- multimerizace proteinu fyziologie MeSH
- myši knockoutované MeSH
- regulace genové exprese účinky léků fyziologie MeSH
- signální transdukce fyziologie MeSH
- studie případů a kontrol MeSH
- systémová sklerodermie metabolismus patologie MeSH
- transformující růstový faktor beta farmakologie MeSH
- transkripční faktor Twist biosyntéza nedostatek genetika metabolismus fyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- jaderné proteiny MeSH
- malá interferující RNA MeSH
- messenger RNA MeSH
- transformující růstový faktor beta MeSH
- transkripční faktor Twist MeSH
- TWIST1 protein, human MeSH Prohlížeč
- Twist1 protein, mouse MeSH Prohlížeč
OBJECTIVES: TWIST1 is a member of the class B of basic helix-loop-helix transcription factors that regulates cell lineage determination and differentiation and has been implicated in epithelial-to-mesenchymal transition. Here, we aimed to investigate the role of TWIST1 for the activation of resident fibroblasts in systemic sclerosis (SSc). METHODS: The expression of Twist1 in fibroblasts was modulated by forced overexpression or siRNA-mediated knockdown. Interaction of Twist1, E12 and inhibitor Of differentiation (Id) was analysed by co-immunoprecipitation. The role of Twist1 in vivo was evaluated using inducible, conditional knockout mice with either ubiquitous or fibroblast-specific depletion of Twist1. Mice were either challenged with bleomycin or overexpressing a constitutively active transforming growth factor (TGF)β receptor I. RESULT: The expression of TWIST1 was increased in fibroblasts in fibrotic human and murine skin in a TGFβ/SMAD3-dependent manner. TWIST1 in turn enhanced TGFβ-induced fibroblast activation in a p38-dependent manner. The stimulatory effects of TWIST1 on resident fibroblasts were mediated by TWIST1 homodimers. TGFβ promotes the formation of TWIST1 homodimers by upregulation of TWIST1 and by induction of inhibitor of DNA-binding proteins, which have high affinity for E12/E47 and compete against TWIST1 for E12/E47 binding. Mice with selective depletion of Twist1 in fibroblasts are protected from experimental skin fibrosis in different murine models to a comparable degree as mice with ubiquitous depletion of Twist1. CONCLUSIONS: Our data identify TWIST1 as a central pro-fibrotic factor in SSc, which facilitates fibroblast activation by amplifying TGFβ signalling. Targeting of TWIST1 may thus be a novel approach to normalise aberrant TGFβ signalling in SSc.
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