4.7 Article

ATP spreads inflammation to other limbs through crosstalk between sensory neurons and interneurons

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 219, Issue 6, Pages -

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20212019

Keywords

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Funding

  1. KAKENHI, Q-Leap [JPMXS0120330644]
  2. Japan Agency for Medical Research and Development
  3. Takeda Science Foundation
  4. Institute for Fermentation Osaka
  5. Mitsubishi Foundation
  6. Chugai Pharma Research Grant
  7. Akiyama Life Science Foundation
  8. Institute for Genetic Medicine, Hokkaido University
  9. Photo-excitonix Project, Hokkaido University
  10. Promotion Project for Young Investigators at Hokkaido University

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Local inflammation is spread to remote positions through sensory neuron-interneuron crosstalk using ATP. This neural pathway, known as the remote inflammation gateway reflex, may serve as a therapeutic target for inflammatory diseases with remote inflammation, such as rheumatoid arthritis.
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. Local inflammation spreads to remote positions via sensory neuron-interneuron crosstalk using ATP. This neural pathway, or remote inflammation gateway reflex, may be a therapeutic target for inflammatory diseases with remote inflammation, such as rheumatoid arthritis.

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