Priming mobilization of hair follicle stem cells triggers permanent loss of regeneration after alkylating chemotherapy

Nat Commun. 2019 Aug 27;10(1):3694. doi: 10.1038/s41467-019-11665-0.

Abstract

The maintenance of genetic integrity is critical for stem cells to ensure homeostasis and regeneration. Little is known about how adult stem cells respond to irreversible DNA damage, resulting in loss of regeneration in humans. Here, we establish a permanent regeneration loss model using cycling human hair follicles treated with alkylating agents: busulfan followed by cyclophosphamide. We uncover the underlying mechanisms by which hair follicle stem cells (HFSCs) lose their pool. In contrast to immediate destructive changes in rapidly proliferating hair matrix cells, quiescent HFSCs show unexpected massive proliferation after busulfan and then undergo large-scale apoptosis following cyclophosphamide. HFSC proliferation is activated through PI3K/Akt pathway, and depletion is driven by p53/p38-induced cell death. RNA-seq analysis shows that HFSCs experience mitotic catastrophe with G2/M checkpoint activation. Our findings indicate that priming mobilization causes stem cells to lose their resistance to DNA damage, resulting in permanent loss of regeneration after alkylating chemotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alkylating Agents / pharmacology*
  • Animals
  • Apoptosis / drug effects
  • Busulfan / pharmacology*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cyclophosphamide / pharmacology*
  • DNA Damage / drug effects
  • DNA Damage / genetics
  • Female
  • Hair Follicle / cytology*
  • Hair Follicle / transplantation
  • Heterografts
  • Humans
  • Mice
  • Mice, SCID
  • Middle Aged
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Regeneration / drug effects*
  • Stem Cells / cytology
  • Stem Cells / drug effects*
  • Transplantation, Heterologous
  • Tumor Suppressor Protein p53 / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Alkylating Agents
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Cyclophosphamide
  • Proto-Oncogene Proteins c-akt
  • p38 Mitogen-Activated Protein Kinases
  • Busulfan