@article {1623371,
	title = {Receptor interacting protein 3 kinase, not 1 kinase, through MLKL-mediated necroptosis is involved in UVA-induced corneal endothelium cell death},
	journal = {Cell Death Discov},
	volume = {7},
	number = {1},
	year = {2021},
	month = {2021 Nov 23},
	pages = {366},
	abstract = {Ultraviolet (UV) is one of the most energetic radiations in the solar spectrum that can result in various tissue injury disorders. Previous studies demonstrated that UVA, which represents 95\% of incident photovoltaic radiation, induces corneal endothelial cells (CECs) death. Programmed cell death (PCD) has been implicated in numerous ophthalmologic diseases. Here, we investigated receptor-interacting protein 3 kinase (RIPK3), a key signaling molecule of PCD, in UVA-induced injury using a short-term corneal endothelium (CE) culture model. UVA irradiation activated RIPK3 and mediated necroptosis both in mouse CE and primary human CECs (pHCECs). UVA irradiation was associated with upregulation of key necroptotic molecules (DAI, TRIF, and MLKL) that lie downstream of RIPK3. Moreover, RIPK3 inhibition or silencing in primary corneal endothelial cells suppresses UVA-induced cell death, along with downregulation of MLKL in pHCECs. In addition, genetic inhibition or knockout of RIPK3 in mice (RIPK3K51A and RIPK3-/- mice) similarly attenuates cell death and the levels of necroptosis in ex vivo UVA irradiation experiments. In conclusion, these results identify RIPK3, not RIPK1, as a critical regulator of UVA-induced cell death in CE and indicate its potential as a future protective target.},
	issn = {2058-7716},
	doi = {10.1038/s41420-021-00757-w},
	author = {Yu, Zhen and Efstathiou, Nikolaos E and Correa, Victor S M C and Chen, XiaoHong and Ishihara, Kenji and Iesato, Yasuhiro and Narimatsu, Toshio and Ntentakis, Dimitrios and Chen, Yanyun and Vavvas, Demetrios G}
}
