Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration

Many brain pathologies are associated with liver damage, but a direct link has long remained elusive. Here, we establish a new paradigm for interrogating brain-periphery interactions by leveraging zebrafish for its unparalleled access to the intact whole animal for in vivo analysis in real time afte...

Full description

Bibliographic Details
Main Authors: Linlin Yang, Jessica A Jiménez, Alison M Earley, Victoria Hamlin, Victoria Kwon, Cameron T Dixon, Celia E Shiau
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-07-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/58191
id doaj-63578c8c2f594733bb8315190f69c3ec
record_format Article
spelling doaj-63578c8c2f594733bb8315190f69c3ec2021-05-05T21:22:06ZengeLife Sciences Publications LtdeLife2050-084X2020-07-01910.7554/eLife.58191Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltrationLinlin Yang0https://orcid.org/0000-0001-5602-4157Jessica A Jiménez1Alison M Earley2https://orcid.org/0000-0003-1889-9221Victoria Hamlin3Victoria Kwon4Cameron T Dixon5Celia E Shiau6https://orcid.org/0000-0002-9347-9158Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, United States; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, United StatesMany brain pathologies are associated with liver damage, but a direct link has long remained elusive. Here, we establish a new paradigm for interrogating brain-periphery interactions by leveraging zebrafish for its unparalleled access to the intact whole animal for in vivo analysis in real time after triggering focal brain inflammation. Using traceable lipopolysaccharides (LPS), we reveal that drainage of these inflammatory macromolecules from the brain led to a strikingly robust peripheral infiltration of macrophages into the liver independent of Kupffer cells. We further demonstrate that this macrophage recruitment requires signaling from the cytokine IL-34 and Toll-like receptor adaptor MyD88, and occurs in coordination with neutrophils. These results highlight the possibility for circulation of brain-derived substances to serve as a rapid mode of communication from brain to the liver. Understanding how the brain engages the periphery at times of danger may offer new perspectives for detecting and treating brain pathologies.https://elifesciences.org/articles/58191inflammationmacrophageliver infiltrationneutrophilsbrain drainagekupffer cells
collection DOAJ
language English
format Article
sources DOAJ
author Linlin Yang
Jessica A Jiménez
Alison M Earley
Victoria Hamlin
Victoria Kwon
Cameron T Dixon
Celia E Shiau
spellingShingle Linlin Yang
Jessica A Jiménez
Alison M Earley
Victoria Hamlin
Victoria Kwon
Cameron T Dixon
Celia E Shiau
Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
eLife
inflammation
macrophage
liver infiltration
neutrophils
brain drainage
kupffer cells
author_facet Linlin Yang
Jessica A Jiménez
Alison M Earley
Victoria Hamlin
Victoria Kwon
Cameron T Dixon
Celia E Shiau
author_sort Linlin Yang
title Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
title_short Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
title_full Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
title_fullStr Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
title_full_unstemmed Drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
title_sort drainage of inflammatory macromolecules from the brain to periphery targets the liver for macrophage infiltration
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-07-01
description Many brain pathologies are associated with liver damage, but a direct link has long remained elusive. Here, we establish a new paradigm for interrogating brain-periphery interactions by leveraging zebrafish for its unparalleled access to the intact whole animal for in vivo analysis in real time after triggering focal brain inflammation. Using traceable lipopolysaccharides (LPS), we reveal that drainage of these inflammatory macromolecules from the brain led to a strikingly robust peripheral infiltration of macrophages into the liver independent of Kupffer cells. We further demonstrate that this macrophage recruitment requires signaling from the cytokine IL-34 and Toll-like receptor adaptor MyD88, and occurs in coordination with neutrophils. These results highlight the possibility for circulation of brain-derived substances to serve as a rapid mode of communication from brain to the liver. Understanding how the brain engages the periphery at times of danger may offer new perspectives for detecting and treating brain pathologies.
topic inflammation
macrophage
liver infiltration
neutrophils
brain drainage
kupffer cells
url https://elifesciences.org/articles/58191
work_keys_str_mv AT linlinyang drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT jessicaajimenez drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT alisonmearley drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT victoriahamlin drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT victoriakwon drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT camerontdixon drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
AT celiaeshiau drainageofinflammatorymacromoleculesfromthebraintoperipherytargetstheliverformacrophageinfiltration
_version_ 1721458124930416640