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      Lipid peroxidation regulates long-range wound detection through 5-lipoxygenase in zebrafish.

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          Abstract

          Rapid wound detection by distant leukocytes is essential for antimicrobial defense and post-infection survival 1 . The reactive oxygen species hydrogen peroxide and the polyunsaturated fatty acid arachidonic acid are among the earliest known mediators of this process 2- 4 . It is unknown whether or how these highly conserved cues collaborate to achieve wound detection over distances of several hundreds of microns within a few minutes. To investigate this, we locally applied arachidonic acid and skin permeable peroxide by micropipette perfusion to unwounded zebrafish tail fins. As in wounds, arachidonic acid rapidly attracted leukocytes through dual oxidase (Duox) and 5-lipoxygenase (Alox5a). Peroxide promoted chemotaxis to arachidonic acid without being chemotactic on its own. Intravital biosensor imaging showed that wound peroxide and arachidonic acid converged on half-millimeter long lipid peroxidation gradients that promoted leukocyte attraction. Our data suggest that lipid peroxidation functions as spatial redox relay that enables long-range detection of early wound cues by immune cells, outlining a beneficial role for this otherwise toxic process.

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          Most cited references40

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          Fiji: an open-source platform for biological-image analysis.

          Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis. Fiji uses modern software engineering practices to combine powerful software libraries with a broad range of scripting languages to enable rapid prototyping of image-processing algorithms. Fiji facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system. We propose Fiji as a platform for productive collaboration between computer science and biology research communities.
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            Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis.

            Ferroptosis is form of regulated nonapoptotic cell death that is involved in diverse disease contexts. Small molecules that inhibit glutathione peroxidase 4 (GPX4), a phospholipid peroxidase, cause lethal accumulation of lipid peroxides and induce ferroptotic cell death. Although ferroptosis has been suggested to involve accumulation of reactive oxygen species (ROS) in lipid environments, the mediators and substrates of ROS generation and the pharmacological mechanism of GPX4 inhibition that generates ROS in lipid environments are unknown. We report here the mechanism of lipid peroxidation during ferroptosis, which involves phosphorylase kinase G2 (PHKG2) regulation of iron availability to lipoxygenase enzymes, which in turn drive ferroptosis through peroxidation of polyunsaturated fatty acids (PUFAs) at the bis-allylic position; indeed, pretreating cells with PUFAs containing the heavy hydrogen isotope deuterium at the site of peroxidation (D-PUFA) prevented PUFA oxidation and blocked ferroptosis. We further found that ferroptosis inducers inhibit GPX4 by covalently targeting the active site selenocysteine, leading to accumulation of PUFA hydroperoxides. In summary, we found that PUFA oxidation by lipoxygenases via a PHKG2-dependent iron pool is necessary for ferroptosis and that the covalent inhibition of the catalytic selenocysteine in Gpx4 prevents elimination of PUFA hydroperoxides; these findings suggest new strategies for controlling ferroptosis in diverse contexts.
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              A tissue-scale gradient of hydrogen peroxide mediates rapid wound detection in zebrafish

              Barrier structures (e.g. epithelia around tissues, plasma membranes around cells) are required for internal homeostasis and protection from pathogens. Wound detection and healing represent a dormant morphogenetic program that can be rapidly executed to restore barrier integrity and tissue homeostasis. In animals, initial steps include recruitment of leukocytes to the site of injury across distances of hundreds of micrometers within minutes of wounding. The spatial signals that direct this immediate tissue response are unknown. Due to their fast diffusion and versatile biological activities, reactive oxygen species (ROS), including hydrogen peroxide (H2O2), are interesting candidates for wound-to-leukocyte signalling. We probed the role of H2O2 during the early events of wound responses in zebrafish larvae expressing a genetically encoded H2O2 sensor1. This reporter revealed a sustained rise in H2O2 concentration at the wound margin, starting ∼3 min after wounding and peaking at ∼20 min, which extended ∼100−200 μm into the tail fin epithelium as a decreasing concentration gradient. Using pharmacological and genetic inhibition, we show that this gradient is created by Dual oxidase (Duox), and that it is required for rapid recruitment of leukocytes to the wound. This is the first observation of a tissue-scale H2O2 pattern, and the first evidence that H2O2 signals to leukocytes in tissues, in addition to its known antiseptic role.
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                Author and article information

                Journal
                100890575
                21417
                Nat Cell Biol
                Nat Cell Biol
                Nature cell biology
                1465-7392
                1476-4679
                30 July 2020
                31 August 2020
                September 2020
                28 February 2021
                : 22
                : 9
                : 1049-1055
                Affiliations
                [1 ]Cell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA
                [2 ]Louis V. Gerstner, Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA
                [3 ]University of North Carolina at Chapel Hill School of Medicine, Department of Cell Biology and Physiology, Chapel Hill, NC 27599, USA
                [4 ]equally contributed
                Author notes
                [5 ]correspondence: niethamp@ 123456mskcc.org

                Author Contributions

                PN conceived the study and its experiments and conducted them with AK. MJ generated and characterized the alox5a mutant fish. GFG generated and characterized the alox12 mutant fish. YM performed Sudan blacks staining of leukocytes. MO provided general advice on ferroptotic mechanisms. PN analyzed the data, prepared the figures, and wrote the paper together with AK, MJ, GFG, and MO.

                Article
                NIHMS1615044
                10.1038/s41556-020-0564-2
                7898270
                32868902
                c32b902f-fb0b-476c-bb63-2d97f3e482fd

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                Cell biology
                Cell biology

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