Macrophages induce AKT/β-catenin-dependent Lgr5<sup>+</sup> stem cell activation and hair follicle regeneration through TNF.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28345588.
- Also identified by DOI 10.1038/ncomms14091 and PMC identifier 5378973.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Skin stem cells can regenerate epidermal appendages; however, hair follicles (HF) lost as a result of injury are barely regenerated. Here we show that macrophages in wounds activate HF stem cells, leading to telogen-anagen transition (TAT) around the wound and de novo HF regeneration, mostly through TNF signalling. Both TNF knockout and overexpression attenuate HF neogenesis in wounds, suggesting dose-dependent induction of HF neogenesis by TNF, which is consistent with TNF-induced AKT signalling in epidermal stem cells in vitro. TNF-induced β-catenin accumulation is dependent on AKT but not Wnt signalling. Inhibition of PI3K/AKT blocks depilation-induced HF TAT. Notably, Pten loss in Lgr5<sup>+</sup> HF stem cells results in HF TAT independent of injury and promotes HF neogenesis after wounding. Thus, our results suggest that macrophage-TNF-induced AKT/β-catenin signalling in Lgr5<sup>+</sup> HF stem cells has a crucial role in promoting HF cycling and neogenesis after wounding.
Medical subject headings
- Hair Follicle
- Macrophages
- Regeneration
- Stem Cells
- Tumor Necrosis Factor-alpha