Inhibition of caspase-11 under inflammatory conditions suppresses chondrogenic differentiation
Jazyk angličtina Země Scotland Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38875922
DOI
10.1016/j.tice.2024.102425
PII: S0040-8166(24)00126-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cartilage, Caspase-11, Chondrogenesis, Inflammation, Osteoarthritis,
- MeSH
- buněčná diferenciace * MeSH
- chondrocyty metabolismus cytologie MeSH
- chondrogeneze * MeSH
- chrupavka metabolismus MeSH
- cytokiny metabolismus MeSH
- iniciační kaspasy * metabolismus MeSH
- kaspasy metabolismus MeSH
- myši MeSH
- zánět * patologie metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- Casp4 protein, mouse MeSH Prohlížeč
- cytokiny MeSH
- iniciační kaspasy * MeSH
- kaspasy MeSH
Caspase-11 is the murine homologue of human caspases-4 and -5 and is involved in mediating the inflammatory response. However, its functions are often confused and misinterpreted with the more important and better described caspase-1. Therefore, this study focused exclusively on the specific roles of caspase-11, both in cartilage formation and in the inflammatory environment. The presence of caspase-11 during mouse limb development and in chondrogenic cell cultures was investigated by immunofluorescence detection. Subsequently, the function of caspase-11 was downregulated and the affected molecules investigated. The expression analysis applied for osteo/chondrogenesis associated factors and inflammatory cytokines. Simultaneously, morphological appearance of the micromass cultures was evaluated. The results revealed that caspase-11 is physiologically present during cartilage development, but its inhibition under physiological conditions has no significant effect on chondrogenic differentiation. However, in an inflammatory environment, inhibition and downregulation of caspase-11 leads to reduced differentiation of cartilage nodules. Additionally, reduced expression of several genes including Col2a1 and Sp7 and conversely increased expression of Mmp9 were observed. In the cytokine expression panel, a significant decrease was found in molecules that, along with the inflammatory function, may also be involved in cartilage differentiation. The findings bring new information about caspase-11 in chondrogenesis and show that its downregulation under inflammatory conditions reduces cartilage formation.
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