JMJD3 activated hyaluronan synthesis drives muscle regeneration in an inflammatory environment - Archive ouverte HAL
Article Dans Une Revue Science Année : 2022

JMJD3 activated hyaluronan synthesis drives muscle regeneration in an inflammatory environment

Kiran Nakka
Sarah Hachmer
  • Fonction : Auteur
Zeinab Mokhtari
Radmila Kovac
Clara Bernard
Guojia Xie
  • Fonction : Auteur
Magid Fallahi
  • Fonction : Auteur
Lynn Megeney
Julien Gondin
Bénédicte Chazaud
Marjorie Brand
Xiaohui Zha
  • Fonction : Auteur
Kai Ge

Résumé

Muscle stem cells (MuSCs) reside in a specialized niche that ensures their regenerative capacity. Although we know that innate immune cells infiltrate the niche in response to injury, it remains unclear how MuSCs adapt to this altered environment for initiating repair. Here, we demonstrate that inflammatory cytokine signaling from the regenerative niche impairs the ability of quiescent MuSCs to reenter the cell cycle. The histone H3 lysine 27 (H3K27) demethylase JMJD3, but not UTX, allowed MuSCs to overcome inhibitory inflammation signaling by removing trimethylated H3K27 (H3K27me3) marks at the Has2 locus to initiate production of hyaluronic acid, which in turn established an extracellular matrix competent for integrating signals that direct MuSCs to exit quiescence. Thus, JMJD3-driven hyaluronic acid synthesis plays a proregenerative role that allows MuSC adaptation to inflammation and the initiation of muscle repair.
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Dates et versions

hal-03766492 , version 1 (28-11-2022)

Identifiants

Citer

Kiran Nakka, Sarah Hachmer, Zeinab Mokhtari, Radmila Kovac, Hina Bandukwala, et al.. JMJD3 activated hyaluronan synthesis drives muscle regeneration in an inflammatory environment. Science, 2022, 377 (6606), pp.666-669. ⟨10.1126/science.abm9735⟩. ⟨hal-03766492⟩
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