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Inflammation modulates intercellular adhesion and mechanotransduction in human epidermis via ROCK2.


ABSTRACT: Aberrant mechanotransduction and compromised epithelial barrier function are associated with numerous human pathologies including inflammatory skin disorders. However, the cytoskeletal mechanisms regulating inflammatory responses in the epidermis are not well understood. Here we addressed this question by inducing a psoriatic phenotype in human keratinocytes and reconstructed human epidermis using a cytokine stimulation model. We show that the inflammation upregulates the Rho-myosin II pathway and destabilizes adherens junctions (AJs) promoting YAP nuclear entry. The integrity of cell-cell adhesion but not the myosin II contractility per se is the determinative factor for the YAP regulation in epidermal keratinocytes. The inflammation-induced disruption of AJs, increased paracellular permeability, and YAP nuclear translocation are regulated by ROCK2, independently from myosin II activation. Using a specific inhibitor KD025, we show that ROCK2 executes its effects via cytoskeletal and transcription-dependent mechanisms to shape the inflammatory response in the epidermis.

SUBMITTER: Shutova MS 

PROVIDER: S-EPMC9986521 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature

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Inflammation modulates intercellular adhesion and mechanotransduction in human epidermis via ROCK2.

Shutova Maria S MS   Borowczyk Julia J   Russo Barbara B   Sellami Sihem S   Drukala Justyna J   Wolnicki Michal M   Brembilla Nicolo C NC   Kaya Gurkan G   Ivanov Andrei I AI   Boehncke Wolf-Henning WH  

iScience 20230214 3


Aberrant mechanotransduction and compromised epithelial barrier function are associated with numerous human pathologies including inflammatory skin disorders. However, the cytoskeletal mechanisms regulating inflammatory responses in the epidermis are not well understood. Here we addressed this question by inducing a psoriatic phenotype in human keratinocytes and reconstructed human epidermis using a cytokine stimulation model. We show that the inflammation upregulates the Rho-myosin II pathway a  ...[more]

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