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A Chemical Genetic Screen Identifies ABHD12 as an Oxidized Phosphatidylserine Lipase

Reactive oxygen species (ROS) are transient, highly reactive intermediates or byproducts produced during oxygen metabolism. However, when innate mechanisms are unable to cope with sequestration of surplus ROS, it causes oxidative stress, where excess ROS damage biomolecules. Oxidized phosphatidylser...

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Detalles Bibliográficos
Autores principales: Kelkar, Dhanashree S., Ravikumar, Govindan, Mehendale, Neelay, Singh, Shubham, Joshi, Alaumy, Sharma, Ajay Kumar, Mhetre, Amol, Rajendran, Abinaya, Chakrapani, Harinath, Kamat, Siddhesh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6420073/
https://www.ncbi.nlm.nih.gov/pubmed/30643283
http://dx.doi.org/10.1038/s41589-018-0195-0
Descripción
Sumario:Reactive oxygen species (ROS) are transient, highly reactive intermediates or byproducts produced during oxygen metabolism. However, when innate mechanisms are unable to cope with sequestration of surplus ROS, it causes oxidative stress, where excess ROS damage biomolecules. Oxidized phosphatidylserine (PS), a pro-apoptotic “eat me” signal, is produced in response to elevated ROS, yet, little is known of its chemical composition and metabolism. Here, we report a small molecule that generates ROS in different mammalian cells, using which we detect, characterize and study oxidized PS in mammalian cells. We describe a chemical genetic screen to identify enzymes that regulate oxidized PS in mammalian cells, and find that the lipase ABHD12 hydrolyzes oxidized PS. We validate these findings in different physiological settings including primary peritoneal macrophages, and brains from Abhd12(–/–) knockout mice under inflammatory stress, and in the process functionally annotate an enzyme capable of regulating oxidized PS in vivo.