Dynasore Protects Corneal Epithelial Cells Subjected to Hyperosmolar Stress in an In Vitro Model of Dry Eye Epitheliopathy
Autor: | Rafael Martinez-Carrasco, M. Elizabeth Fini |
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Jazyk: | angličtina |
Rok vydání: | 2023 |
Předmět: |
corneal epithelium
ocular surface Organic Chemistry General Medicine unfolded protein response Catalysis Computer Science Applications Inorganic Chemistry dry eye epitheliopathy endoplasmic reticulum stress oxidative stress dynasore Physical and Theoretical Chemistry Molecular Biology Spectroscopy hyperosmolar stress |
Zdroj: | International Journal of Molecular Sciences Volume 24 Issue 5 Pages: 4754 |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms24054754 |
Popis: | Epitheliopathy at the ocular surface is a defining sign of dry eye disease, a common disorder that affects 10% to 30% of the world’s population. Hyperosmolarity of the tear film is one of the main drivers of pathology, with subsequent endoplasmic reticulum (ER) stress, the resulting unfolded protein response (UPR), and caspase-3 activation implicated in the pathway to programmed cell death. Dynasore, is a small molecule inhibitor of dynamin GTPases that has shown therapeutic effects in a variety of disease models involving oxidative stress. Recently we showed that dynasore protects corneal epithelial cells exposed to the oxidant tBHP, by selective reduction in expression of CHOP, a marker of the UPR PERK branch. Here we investigated the capacity of dynasore to protect corneal epithelial cells subjected to hyperosmotic stress (HOS). Similar to dynasore’s capacity to protect against tBHP exposure, dynasore inhibits the cell death pathway triggered by HOS, protecting against ER stress and maintaining a homeostatic level of UPR activity. However, unlike with tBHP exposure, UPR activation due to HOS is independent of PERK and mostly driven by the UPR IRE1 branch. Our results demonstrate the role of the UPR in HOS-driven damage, and the potential of dynasore as a treatment to prevent dry eye epitheliopathy. |
Databáze: | OpenAIRE |
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