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Ferroptosis of select skin epithelial cells initiates and maintains chronic systemic immune-mediated psoriatic disease
Kavita Vats, … , Valerian E. Kagan, Yuri L. Bunimovich
Kavita Vats, … , Valerian E. Kagan, Yuri L. Bunimovich
Published November 21, 2024
Citation Information: J Clin Invest. 2025;135(2):e183219. https://doi.org/10.1172/JCI183219.
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Research Article Dermatology Inflammation Article has an altmetric score of 13

Ferroptosis of select skin epithelial cells initiates and maintains chronic systemic immune-mediated psoriatic disease

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Abstract

Dysregulations of epithelial-immune interactions frequently culminate in chronic inflammatory diseases of the skin, lungs, kidneys, and gastrointestinal tract. Yet, the intraepithelial processes that initiate and perpetuate inflammation in these organs are poorly understood. Here, by utilizing redox lipidomics we identified ferroptosis-associated peroxidation of polyunsaturated phosphatidylethanolamines in the epithelia of patients with asthma, cystic fibrosis, psoriasis, and renal failure. Focusing on psoriasis as a disease model, we used high-resolution mass spectrometry imaging and identified keratin 14–expressing (K14-expressing) keratinocytes executing a ferroptotic death program in human psoriatic skin. Psoriatic phenotype with characteristic Th1/Th17 skin and extracutaneous immune responses was initiated and maintained in a murine model designed to actuate ferroptosis in a fraction of K14+ glutathione peroxidase 4–deficient (Gpx4-deficient) epidermal keratinocytes. Importantly, an antiferroptotic agent, liproxstatin-1, was as effective as clinically relevant biological IL-12/IL-23/TNF-α–targeting therapies or the depletion of T cells in completely abrogating molecular, biochemical, and morphological features of psoriasis. As ferroptosis in select epidermal keratinocytes triggers and sustains a pathological psoriatic multiorgan inflammatory circuit, we suggest that strategies targeting ferroptosis or its causes may be effective in preventing or ameliorating a variety of chronic inflammatory diseases.

Authors

Kavita Vats, Hua Tian, Kunal Singh, Yulia Y. Tyurina, Louis J. Sparvero, Vladimir A. Tyurin, Oleg Kruglov, Alexander Chang, Jiefei Wang, Felicia Green, Svetlana N. Samovich, Jiying Zhang, Ansuman Chattopadhyay, Natalie Murray, Vrusha K. Shah, Alicia R. Mathers, Uma R. Chandran, Joseph M. Pilewski, John A. Kellum, Sally E. Wenzel, Hülya Bayır, Valerian E. Kagan, Yuri L. Bunimovich

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Figure 2

Elevated oxPE ferroptosis death signals in psoriatic epidermis are overrepresented within the K14+ KCs.

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Elevated oxPE ferroptosis death signals in psoriatic epidermis are overr...
(A) Overlay of MALDI-MS and IF imaging of human nonlesional (control) skin (left) and psoriatic skin (right). MALDI-MS ratiometric grayscale images (20 μm raster, negative ion mode) show the abundance ratio of detected m/z 826.6 to 794.6 ions, corresponding to PE(40:4)+2O and PE(40:4), respectively. Scale bars: 100 μm. PanCK, pan-cytokeratin. (B) MALDI-MS signal intensities (single pixel) of oxPE/PE [PE(40:4)+2O/PE(40:4), PE(40:4)+3O/PE(40:4)] in panCK+K14– and K14+ regions of control and psoriatic epidermides. Numbers of pixels in each group are indicated over the first violin plot. (C) C60-SIMS imaging of K14+ and panCK+ cells in control skin (top) and psoriatic skin (bottom). Scale bars: 50 μm. Regions within dashed rectangles are shown magnified in D. (D) Overlay of panCK+ and K14+ epidermal regions (obtained by C60-SIMS) and lipids [cholesterol sulfate, PE, and oxPE species; obtained by (H2O)n-GCIB-SIMS] in control skin (top) and psoriatic skin (bottom). Color intensities representing each lipid species were adjusted to match a relative scale of 0 to 100 (color bars). Scale bars: 50 μm. (E) Single-cell (H2O)n-GCIB-SIMS signal intensities of select pro-ferroptotic oxPE species within panCK+K14– and K14+ epidermal KCs in control versus psoriatic skin. Numbers of cells in each group are indicated over the first violin plot. Data are means ± SD. Two-tailed Student’s t test; *P < 0.05.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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