| Literature DB >> 31178398 |
Shahad Albadri1, Federica Naso2, Marion Thauvin3, Carole Gauron3, Carola Parolin4, Karine Duroure5, Juliette Vougny5, Jessica Fiori4, Carla Boga6, Sophie Vriz7, Natalia Calonghi8, Filippo Del Bene9.
Abstract
Reactive oxygen species (ROS) and downstream products of lipid oxidation are emerging as important secondary messengers in tissue homeostasis. However, their regulation and mechanism of action remain poorly studied in vivo during normal development. Here, we reveal that the fine regulation of hydrogen peroxide (H2O2) levels by its scavenger Catalase to mediate the switch from proliferation to differentiation in retinal progenitor cells (RPCs) is crucial. We identify 9-hydroxystearic acid (9-HSA), an endogenous downstream lipid peroxidation product, as a mediator of this effect in the zebrafish retina. We show that the 9-HSA proliferative effect is due to the activation of Notch and Wnt pathways through the inhibition of the histone deacetylase 1. We show that the local and temporal manipulation of H2O2 levels in RPCs is sufficient to trigger their premature differentiation. We finally propose a mechanism that links H2O2 homeostasis and neuronal differentiation via the modulation of lipid peroxidation.Entities:
Keywords: 9-hydroxystearic acid; H(2)O(2); HDAC1; lipid peroxidation; neuronal differentiation; redox signaling; retinal progenitor cells; stem cell metabolism; zebrafish
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Year: 2019 PMID: 31178398 DOI: 10.1016/j.devcel.2019.05.011
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270