Department of Dermatology, Seoul National University College of Medicine, Seoul, 03080, Korea.
Institute of Human-Environment Interface Biology, Medical Research Center, Seoul National University, Seoul, 03080, Korea.
Nat Commun. 2019 Aug 27;10(1):3694. doi: 10.1038/s41467-019-11665-0.
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.
维持遗传完整性对于干细胞确保体内平衡和再生至关重要。目前尚不清楚成年干细胞如何应对不可逆的 DNA 损伤,从而导致人类再生能力丧失。在这里,我们使用烷化剂:白消安(busulfan)继之以环磷酰胺处理循环的人毛囊,建立了一个永久性再生丧失模型。我们揭示了毛囊干细胞 (HFSCs) 失去其群体的潜在机制。与快速增殖的毛基质细胞立即发生破坏性变化相反,静止的 HFSCs 在白消安处理后表现出出乎意料的大量增殖,然后在环磷酰胺处理后发生大规模凋亡。HFSC 的增殖通过 PI3K/Akt 途径激活,而耗竭则由 p53/p38 诱导的细胞死亡驱动。RNA-seq 分析表明,HFSCs 经历有丝分裂灾难,G2/M 检查点激活。我们的研究结果表明,启动动员导致干细胞失去对 DNA 损伤的抵抗力,从而导致烷化化疗后永久性再生丧失。