| Literature DB >> 32735214 |
Linlin Yang1, Jessica A Jiménez1, Alison M Earley1, Victoria Hamlin1, Victoria Kwon1, Cameron T Dixon1, Celia E Shiau1,2.
Abstract
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.Entities:
Keywords: brain drainage; immunology; inflammation; kupffer cells; liver infiltration; macrophage; neuroscience; neutrophils; zebrafish
Year: 2020 PMID: 32735214 PMCID: PMC7434444 DOI: 10.7554/eLife.58191
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140