Impaired Keratinocyte Proliferative And Clonogenic Potential In Transgenic Mice Overexpressing 14-3-3σ In The Epidermis

    Francesca Cianfarani, Silvia Bernardini, Naomi De Luca, Elena Dellambra, Laura Tatangelo, Cecilia Tiveron, Carien M. Niessen, Giovanna Zambruno, Daniele Castiglia, Teresa Odorisio
    Studysummary This study found that overexpressing the 14-3-3σ protein in transgenic mice reduced keratinocyte proliferation and migration, leading to thinner epidermis and fewer hair follicles due to IGF-1 pathway inhibition. Our plain-language summary of this paper — not a Tressless recommendation.
    In this study, transgenic mice overexpressing 14-3-3σ in the epidermis showed decreased keratinocyte proliferation and clonogenic potential, leading to reduced epidermal thickness and hair follicle density. The overexpression resulted in a decrease in keratinocyte progenitor cell numbers and impaired response to IGF-1, affecting downstream mediators like PI3K, AKT, and Rac1. Various assays revealed reduced keratinocyte motility and colony-forming capacity in transgenic mice compared to wild-type controls. The study suggested that 14-3-3σ played a role in controlling the epidermal proliferation-differentiation switch by promoting cell cycle exit in keratinocytes, highlighting its potential tumor suppressor function and impact on IGF-1-mediated signaling pathways.
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