Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish

Abstract Neutrophil recruitment to injured tissue appears to be an evolutionarily conserved strategy for organisms to fight against exogenous insults. Recent studies have shown rhythmic migration of neutrophils and several factors, including melatonin, have been implicated in regulating this rhythmi...

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Main Authors: Da-long Ren, Cheng Ji, Xiao-Bo Wang, Han Wang, Bing Hu
Format: Article
Language:English
Published: Nature Publishing Group 2017-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-05074-w
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spelling doaj-f18889151ab64d6c8279edb0412b2cf72020-12-08T01:15:19ZengNature Publishing GroupScientific Reports2045-23222017-07-017111010.1038/s41598-017-05074-wEndogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafishDa-long Ren0Cheng Ji1Xiao-Bo Wang2Han Wang3Bing Hu4Chinese Academy of Sciences Key Laboratory of Brain Function and Disease, School of Life Sciences, University of Science and Technology of ChinaCenter for Circadian Clocks, Soochow UniversityChinese Academy of Sciences Key Laboratory of Brain Function and Disease, School of Life Sciences, University of Science and Technology of ChinaCenter for Circadian Clocks, Soochow UniversityChinese Academy of Sciences Key Laboratory of Brain Function and Disease, School of Life Sciences, University of Science and Technology of ChinaAbstract Neutrophil recruitment to injured tissue appears to be an evolutionarily conserved strategy for organisms to fight against exogenous insults. Recent studies have shown rhythmic migration of neutrophils and several factors, including melatonin, have been implicated in regulating this rhythmic migration. The mechanisms underlying how endogenous melatonin regulates rhythmic neutrophils migration, however, are unclear. Here we generated a zebrafish annat2 mutant that lacks endogenous melatonin and, subsequently, a Tg(lyz:EGFP);aanat2 −/− transgenic line that allows for monitoring neutrophils migration visually in live zebrafish. We observed that migrating neutrophils are significantly reduced in aanat2 −/− mutant zebrafish under a light/dark condition, and the disrupted migrating rhythmicity of neutrophils in aanat2 −/− zebrafish is independent of the circadian clock. Further, we also found that endogenous melatonin enhances neutrophils migration likely by inducing the expression of cytokines such as interleukin-8 and interleukin-1β. Together, our findings provide evidence that endogenous melatonin promotes rhythmic migration of neutrophils through cytokines in zebrafish.https://doi.org/10.1038/s41598-017-05074-w
collection DOAJ
language English
format Article
sources DOAJ
author Da-long Ren
Cheng Ji
Xiao-Bo Wang
Han Wang
Bing Hu
spellingShingle Da-long Ren
Cheng Ji
Xiao-Bo Wang
Han Wang
Bing Hu
Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
Scientific Reports
author_facet Da-long Ren
Cheng Ji
Xiao-Bo Wang
Han Wang
Bing Hu
author_sort Da-long Ren
title Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
title_short Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
title_full Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
title_fullStr Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
title_full_unstemmed Endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
title_sort endogenous melatonin promotes rhythmic recruitment of neutrophils toward an injury in zebrafish
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-07-01
description Abstract Neutrophil recruitment to injured tissue appears to be an evolutionarily conserved strategy for organisms to fight against exogenous insults. Recent studies have shown rhythmic migration of neutrophils and several factors, including melatonin, have been implicated in regulating this rhythmic migration. The mechanisms underlying how endogenous melatonin regulates rhythmic neutrophils migration, however, are unclear. Here we generated a zebrafish annat2 mutant that lacks endogenous melatonin and, subsequently, a Tg(lyz:EGFP);aanat2 −/− transgenic line that allows for monitoring neutrophils migration visually in live zebrafish. We observed that migrating neutrophils are significantly reduced in aanat2 −/− mutant zebrafish under a light/dark condition, and the disrupted migrating rhythmicity of neutrophils in aanat2 −/− zebrafish is independent of the circadian clock. Further, we also found that endogenous melatonin enhances neutrophils migration likely by inducing the expression of cytokines such as interleukin-8 and interleukin-1β. Together, our findings provide evidence that endogenous melatonin promotes rhythmic migration of neutrophils through cytokines in zebrafish.
url https://doi.org/10.1038/s41598-017-05074-w
work_keys_str_mv AT dalongren endogenousmelatoninpromotesrhythmicrecruitmentofneutrophilstowardaninjuryinzebrafish
AT chengji endogenousmelatoninpromotesrhythmicrecruitmentofneutrophilstowardaninjuryinzebrafish
AT xiaobowang endogenousmelatoninpromotesrhythmicrecruitmentofneutrophilstowardaninjuryinzebrafish
AT hanwang endogenousmelatoninpromotesrhythmicrecruitmentofneutrophilstowardaninjuryinzebrafish
AT binghu endogenousmelatoninpromotesrhythmicrecruitmentofneutrophilstowardaninjuryinzebrafish
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