Dynamic adult tracheal plasticity drives stem cell adaptation to changes in intestinal homeostasis in Drosophila.
Jessica PerochonYachuan YuGabriel N AugheyAndré B MedinaTony D SouthallJulia B CorderoPublished in: Nature cell biology (2021)
Coordination of stem cell function by local and niche-derived signals is essential to preserve adult tissue homeostasis and organismal health. The vasculature is a prominent component of multiple stem cell niches. However, its role in adult intestinal homeostasis remains largely understudied. Here we uncover a previously unrecognised crosstalk between adult intestinal stem cells in Drosophila and the vasculature-like tracheal system, which is essential for intestinal regeneration. Following damage to the intestinal epithelium, gut-derived reactive oxygen species activate tracheal HIF-1α and bidirectional FGF/FGFR signalling, leading to reversible remodelling of gut-associated terminal tracheal cells and intestinal stem cell proliferation following damage. Unexpectedly, reactive oxygen species-induced adult tracheal plasticity involves downregulation of the tracheal specification factor trachealess (trh) and upregulation of IGF2 messenger RNA-binding protein (IGF2BP2/Imp). Our results reveal an intestine-vasculature inter-organ communication programme that is essential to adapt the stem cell response to the proliferative demands of the intestinal epithelium.
Keyphrases
- stem cells
- cell proliferation
- reactive oxygen species
- binding protein
- healthcare
- signaling pathway
- cell therapy
- gene expression
- oxidative stress
- mesenchymal stem cells
- randomized controlled trial
- induced apoptosis
- pi k akt
- study protocol
- clinical trial
- genome wide
- poor prognosis
- cell cycle arrest
- climate change
- dna methylation
- single cell
- diabetic rats
- bone marrow
- endothelial cells
- public health
- mental health