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An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish

Author

Listed:
  • Nicolas Denans

    (Stowers Institute for Medical Research)

  • Nhung T. T. Tran

    (Stowers Institute for Medical Research)

  • Madeleine E. Swall

    (Stowers Institute for Medical Research)

  • Daniel C. Diaz

    (Stowers Institute for Medical Research
    Parse Biosciences)

  • Jillian Blanck

    (Stowers Institute for Medical Research)

  • Tatjana Piotrowski

    (Stowers Institute for Medical Research)

Abstract

Macrophages are essential for tissue repair and regeneration. Yet, the molecular programs, as well as the timing of their activation during and after tissue injury are poorly defined. Using a high spatio-temporal resolution single cell analysis of macrophages coupled with live imaging after sensory hair cell death in zebrafish, we find that the same population of macrophages transitions through a sequence of three major anti-inflammatory activation states. Macrophages first show a signature of glucocorticoid activation, then IL-10 signaling and finally the induction of oxidative phosphorylation by IL-4/Polyamine signaling. Importantly, loss-of-function of glucocorticoid and IL-10 signaling shows that each step of the sequence is independently activated. Lastly, we show that IL-10 and IL-4 signaling act synergistically to promote synaptogenesis between hair cells and efferent neurons during regeneration. Our results show that macrophages, in addition to a switch from M1 to M2, sequentially and independently transition though three anti-inflammatory pathways in vivo during tissue injury in a regenerating organ.

Suggested Citation

  • Nicolas Denans & Nhung T. T. Tran & Madeleine E. Swall & Daniel C. Diaz & Jillian Blanck & Tatjana Piotrowski, 2022. "An anti-inflammatory activation sequence governs macrophage transcriptional dynamics during tissue injury in zebrafish," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33015-3
    DOI: 10.1038/s41467-022-33015-3
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