| First Author | Vind AC | Year | 2024 |
| Journal | Mol Cell | Volume | 84 |
| Issue | 24 | Pages | 4774-4789.e9 |
| PubMed ID | 39591967 | Mgi Jnum | J:360171 |
| Mgi Id | MGI:7790389 | Doi | 10.1016/j.molcel.2024.10.044 |
| Citation | Vind AC, et al. (2024) The ribotoxic stress response drives acute inflammation, cell death, and epidermal thickening in UV-irradiated skin in vivo. Mol Cell 84(24):4774-4789.e9 |
| abstractText | Solar UVB light causes damage to the outermost layer of skin. This insult induces rapid local responses, such as dermal inflammation, keratinocyte cell death, and epidermal thickening, all of which have traditionally been associated with DNA damage response signaling. Another stress response that is activated by UVB light is the ribotoxic stress response (RSR), which depends on the ribosome-associated mitogen-activated protein 3 kinases (MAP3K) ZAKalpha and culminates in p38 and JNK activation. Using ZAK knockout mice, we here show that it is the RSR that is responsible for the early manifestation of UVB-induced skin inflammation and keratinocyte death and subsequent proliferation in vivo. We also show that the RSR controls both p38-mediated pyroptotic and JNK-mediated apoptotic programmed cell death of human keratinocytes in vitro. In sum, our work highlights that skin cells rely on a cytoplasmic and ribosomal stress signal rather than a nuclear and DNA-templated signal for rapid inflammatory responses to UV exposure. |
