Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation

Ding, Xiaolei and Willenborg, Sebastian and Bloch, Wilhelm and Wickström, Sara A. and Wagle, Prerana and Brodesser, Susanne and Roers, Axel and Jais, Alexander and Brüning, Jens C. and Hall, Michael N. and Rüegg, Markus A. and Eming, Sabine A.. (2020) Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation. Journal of Allergy and Clinical Immunology, 145 (1). pp. 283-300.E8.

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Official URL: https://edoc.unibas.ch/71769/

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Perturbation of epidermal barrier formation will profoundly compromise overall skin function, leading to a dry and scaly, ichthyosis-like skin phenotype, which is the hallmark of a broad range of skin diseases, including ichthyosis, atopic dermatitis, and a multitude of clinical eczema variants. An overarching molecular mechanism that orchestrates the multitude of factors controlling epidermal barrier formation and homeostasis remains to be elucidated.; Here we highlight a specific role of mammalian target of rapamycin complex 2 (mTORC2) signaling in epidermal barrier formation.; Epidermal mTORC2 signaling was specifically disrupted by deleting Rictor, encoding an essential subunit of mTORC2 in mouse epidermis (Ric; EKO; ). Epidermal structure and barrier function were investigated by a combination of gene expression, biochemical, morphological and functional analysis in Ric; EKO; and control mice.; Ric; EKO; newborns displayed an ichthyosis-like phenotype characterized by dysregulated epidermal de novo lipid synthesis, altered lipid lamellae structure, and aberrant filaggrin processing. Despite a compensatory transcriptional epidermal repair response, the protective epidermal function was impaired in Ric; EKO; mice as revealed by increased transepidermal water loss, enhanced corneocyte fragility, decreased dendritic epidermal T cells, and an exaggerated percutaneous immune response. Restoration of Akt-Ser473 phosphorylation in mTORC2-deficient keratinocytes by expression of constitutive Akt rescued filaggrin processing.; Our findings reveal a critical metabolic signaling relay of barrier formation where epidermal mTORC2 activity controls filaggrin processing and de novo epidermal lipid synthesis during cornification. Our findings provide novel mechanistic insights into epidermal barrier formation and could open up new therapeutic opportunities to restore defective epidermal barrier conditions.
Faculties and Departments:05 Faculty of Science > Departement Biozentrum > Growth & Development > Biochemistry (Hall)
05 Faculty of Science > Departement Biozentrum > Neurobiology > Pharmacology/Neurobiology (Rüegg)
UniBasel Contributors:Rüegg, Markus A. and Hall, Michael N.
Item Type:Article, refereed
Article Subtype:Research Article
Note:Publication type according to Uni Basel Research Database: Journal article
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Last Modified:19 Apr 2022 07:03
Deposited On:22 Dec 2020 07:37

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