| Literature DB >> 35579694 |
Rie Hasebe1,2, Kaoru Murakami1, Masaya Harada3, Nada Halaka1, Yuki Tanaka1,4, Hiroshi Nakagawa5, Fuminori Kawano6, Yoshinobu Ohira6, Tadafumi Kawamoto7, Fiona E Yull8, Timothy S Blackwell9, Junko Nio-Kobayashi10, Toshihiko Iwanaga10, Masahiko Watanabe11, Nobuhiro Watanabe12, Harumi Hotta12, Toshihide Yamashita5, Daisuke Kamimura1, Masaaki Murakami1,2,4.
Abstract
Neural circuits between lesions are one mechanism through which local inflammation spreads to remote positions. Here, we show the inflammatory signal on one side of the joint is spread to the other side via sensory neuron-interneuron crosstalk, with ATP at the core. Surgical ablation or pharmacological inhibition of this neural pathway prevented inflammation development on the other side. Mechanistic analysis showed that ATP serves as both a neurotransmitter and an inflammation enhancer, thus acting as an intermediary between the local inflammation and neural pathway that induces inflammation on the other side. These results suggest blockade of this neural pathway, which is named the remote inflammation gateway reflex, may have therapeutic value for inflammatory diseases, particularly those, such as rheumatoid arthritis, in which inflammation spreads to remote positions.Entities:
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Year: 2022 PMID: 35579694 PMCID: PMC9117706 DOI: 10.1084/jem.20212019
Source DB: PubMed Journal: J Exp Med ISSN: 0022-1007 Impact factor: 17.579