Congenital deficiency reveals critical role of ISG15 in skin homeostasis

• Published in: The Journal of clinical investigation 2022-02, Vol.132 (3), p.1-19
• Main Authors: Malik, Muhammad Nasir Hayat, Waqas, Syed Fakhar-Ul-Hassnain, Zeitvogel, Jana, Cheng, Jingyuan, Geffers, Robert, Gouda, Zeinab Abu-Elbaha, Elsaman, Ahmed Mahrous, Radwan, Ahmed R, Schefzyk, Matthias, Braubach, Peter, Auber, Bernd, Olmer, Ruth, Müsken, Mathias, Roesner, Lennart M, Gerold, Gisa, Schuchardt, Sven, Merkert, Sylvia, Martin, Ulrich, Meissner, Felix, Werfel, Thomas, Pessler, Frank
• Format: Article
• Language: English
• Subjects: Age; Autoimmunity; Biomedical research; Biopsy; Case studies; Cell adhesion & migration; Cell Line, Transformed; Cell migration; Collagen; Complications and side effects; Connective tissue; Connective tissues; Convulsions & seizures; Corticosteroids; Cytokines - deficiency; Cytokines - metabolism; Dermis - metabolism; Diagnosis; Doxycycline; Endothelial cells; Epidermis; Etiology; Fibroblasts; Fibroblasts - metabolism; Genetic aspects; Genetic disorders; Health aspects; Homeostasis; Humans; Immunity; Inflammation; Interferon; Keratinocytes; Keratinocytes - metabolism; Lupus; Matrix metalloproteinase; Mutation; Nonsense mutation; Patients; Pediatric research; Phenotypes; Pluripotency; Proteins; Remission (Medicine); Siblings; Skin; Skin diseases; Skin lesions; Stem cells; Steroids; Tuberculosis; Ubiquitins - deficiency; Ubiquitins - metabolism; Ulcers
• ISSN: 1558-8238; 0021-9738; 1558-8238
• DOI: 10.1172/JCI141573

Ulcerating skin lesions are manifestations of human ISG15 deficiency, a type I interferonopathy. However, chronic inflammation may not be their exclusive cause. We describe two siblings with recurrent skin ulcers that healed with scar formation upon corticosteroid treatment. Both had a homozygous nonsense mutation in the ISG15 gene, leading to unstable ISG15 protein lacking the functional domain. We characterized ISG15-/- dermal fibroblasts, HaCaT keratinocytes, and human induced pluripotent stem cell-derived vascular endothelial cells. ISG15-deficient cells exhibited the expected hyperinflammatory phenotype, but also dysregulated expression of molecules critical for connective tissue and epidermis integrity, including reduced collagens and adhesion molecules, but increased matrix metalloproteinases. ISG15-/- fibroblasts exhibited elevated ROS levels and reduced ROS scavenger expression. As opposed to hyperinflammation, defective collagen and integrin synthesis was not rescued by conjugation-deficient ISG15. Cell migration was retarded in ISG15-/- fibroblasts and HaCaT keratinocytes, but normalized under ruxolitinib treatment. Desmosome density was reduced in an ISG15-/- 3D epidermis model. Additionally, there were loose architecture and reduced collagen and desmoglein expression, which could be reversed by treatment with ruxolitinib/doxycycline/TGF-β1. These results reveal critical roles of ISG15 in maintaining cell migration and epidermis and connective tissue homeostasis, whereby the latter likely requires its conjugation to yet unidentified targets.