Evidence for the involvement of keratinocyte-derived microvesicle particles in the photosensitivity associated with xeroderma pigmentosum type A deficiency

• Published in: Photochemistry and photobiology Vol. 100; no. 5; pp. 1457 - 1466
• Main Authors: Christian, Lea, Manjrekar, Pranali, Henkels, Karen M, Rapp, Christine M, Annamraju, Risha, Lohade, Rushabh P, Singh, Shikshita, Carpenter, M Alexandra, Khan, Saman, Kemp, Michael G, Chen, Yanfang, Sahu, Ravi P, Travers, Jeffrey B
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01.09.2024
• Subjects: Animals; Cell-Derived Microparticles - metabolism; Erythema; Humans; Imipramine; Imipramine - pharmacology; Keratinocytes; Keratinocytes - metabolism; Keratinocytes - radiation effects; Lipids; Mice; Mice, Knockout; Photosensitivity; Photosensitivity Disorders; Platelet Activating Factor - metabolism; Platelet-activating factor; Platelet-activating factor receptors; Sphingomyelin phosphodiesterase; Sphingomyelin Phosphodiesterase - deficiency; Sphingomyelin Phosphodiesterase - genetics; Sphingomyelin Phosphodiesterase - metabolism; Therapeutic targets; Ultraviolet radiation; Ultraviolet Rays; Xeroderma pigmentosum; Xeroderma Pigmentosum - genetics; Xeroderma Pigmentosum - metabolism; Xeroderma Pigmentosum Group A Protein - genetics; Xeroderma Pigmentosum Group A Protein - metabolism; Platelet‐activating Factor; UVB; skin; Photosensitivity; Xeroderma pigmentosum type A; mice
• ISSN: 0031-8655; 1751-1097; 1751-1097
• DOI: 10.1111/php.13915

Photosensitivity can be due to numerous causes. The photosensitivity associated with deficiency of xeroderma pigmentosum type A (XPA) has been previously shown to be associated with excess levels of the lipid mediator platelet-activating factor (PAF) generated by the keratinocyte. As PAF has been reported to trigger the production of subcellular microvesicle particles (MVP) due to the enzyme acid sphingomyelinase (aSMase), the goal of these studies was to discern if PAF and aSMase could serve as therapeutic targets for the XPA deficiency photosensitivity. HaCaT keratinocytes lacking XPA generated greater levels of MVP in comparison to control cells. Mice deficient in XPA also generated enhanced MVP levels in skin and in plasma in response to UV radiation. Use of a genetic strategy with mice deficient in both XPA and PAF receptors revealed that these mice generated less MVP release as well as decreased skin erythema and cytokine release compared to XPA knockout mice alone. Finally, the aSMase inhibitor imipramine blocked UV-induced MVP release in HaCaT keratinocytes, as well as XPA knockout mice. These studies support the concept that the photosensitivity associated with XPA involves PAF- and aSMase-mediated MVP release and provides a potential pharmacologic target in treating this form of photosensitivity.