Mitochondrial metabolism coordinates stage-specific repair processes in macrophages during wound healing

Abstract: Wound healing is a coordinated process that initially relies on pro-inflammatory macrophages, followed by a pro-resolution function of these cells. Changes in cellular metabolism likely dictate these distinct activities, but the nature of these changes has been unclear. Here, we profiled early- versus late-stage skin wound macrophages in mice at both the transcriptional and functional levels. We found that glycolytic metabolism in the early phase is not sufficient to ensure productive repair. Instead, by combining conditional disruption of the electron transport chain with deletion of mitochondrial aspartyl-tRNA synthetase, followed by single-cell sequencing analysis, we found that a subpopulation of early-stage wound macrophages are marked by mitochondrial ROS (mtROS) production and HIF1α stabilization, which ultimately drives a pro-angiogenic program essential for timely healing. In contrast, late-phase, pro-resolving wound macrophages are marked by IL-4Rα-mediated mitochondrial respiration and mitohormesis. Collectively, we identify changes in mitochondrial metabolism as a critical control mechanism for macrophage effector functions during wound healing

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Cell metabolism. - 33, 12 (2021) , 2398-2414, ISSN: 1932-7420

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2024
Urheber
Willenborg, Sebastian
Sanin, David E.
Jais, Alexander
Ding, Xiaolei
Ulas, Thomas
Nüchel, Julian
Popović, Milica
MacVicar, Thomas
Langer, Thomas
Schultze, Joachim L.
Gerbaulet, Alexander
Roers, Axel
Pearce, Edward J.
Brüning, Jens Claus
Trifunovic, Aleksandra
Eming, Sabine Anne

DOI
10.1016/j.cmet.2021.10.004
URN
urn:nbn:de:bsz:25-freidok-2480438
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:55 MEZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.

Beteiligte

Entstanden

  • 2024

Ähnliche Objekte (12)