TLDR JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.
The study demonstrated that the JMJD3 and NF-κB-dependent activation of the Notch1 gene was crucial for keratinocyte migration during skin wound healing. Researchers identified Notch1 as a direct target of JMJD3 and NF-κB in wounded keratinocytes, with its up-regulation at the wound edge being essential for the process. Notch1 was found to activate RhoU and PLAU genes, which are important for cell migration. Inactivation of Notch1 led to decreased filopodia formation and increased focal adhesion and actin stress fiber, resulting in reduced keratinocyte migration and impaired wound healing. This highlighted the significance of the JMJD3/NF-κB-Notch pathway in the molecular mechanism of keratinocyte wound healing.
86 citations
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April 2016 in “Nature Communications”
6 citations
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January 2016 in “Journal of Stem Cell Research & Therapy” Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.
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June 2015 in “Stem Cell Research & Therapy” Wnt and Notch signaling help wound healing by promoting cell growth and regulating cell differentiation.
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October 2012 in “Cellular and Molecular Life Sciences” Understanding developmental pathways can improve wound healing treatments.
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June 2020 in “International Journal of Molecular Sciences” Notch signaling disruptions can cause various skin diseases.
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November 2020 in “International Journal of Molecular Sciences” Keratinocytes help heal skin wounds by interacting with immune cells and producing substances that kill pathogens.
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January 2017 in “International Journal of Molecular Sciences” Fat-derived stem cells show promise for skin repair and reducing aging signs but need more research for consistent results.
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