p53 Regulates Progenitor Cell Quiescence and Differentiation in the Airway

被引:56
作者
McConnell, Alicia M. [1 ,2 ,3 ]
Yao, Changfu [1 ,2 ]
Yeckes, Alyson R. [1 ,2 ]
Wang, Yizhou [4 ]
Selvaggio, Anna S. [1 ,2 ]
Tang, Jie [4 ]
Kirsch, David G. [5 ,6 ]
Stripp, Barry R. [1 ,2 ,3 ]
机构
[1] Cedars Sinai Med Ctr, Dept Med, Lung Inst, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Med, Regenerat Med Inst, Los Angeles, CA 90048 USA
[3] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27708 USA
[4] Cedars Sinai Med Ctr, Dept Biomed Sci, Genom Core, Los Angeles, CA 90048 USA
[5] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27708 USA
[6] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27708 USA
关键词
SELF-RENEWAL; DNA-DAMAGE; STEM-CELLS; LUNG; MAINTENANCE; MECHANISMS; REPAIR;
D O I
10.1016/j.celrep.2016.11.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mechanisms that regulate progenitor cell quiescence and differentiation in slowly replacing tissues are not fully understood. Here, we demonstrate that the tumor suppressor p53 regulates both proliferation and differentiation of progenitors in the airway epithelium. p53 loss decreased ciliated cell differentiation and increased the self-renewal and proliferative capacity of club progenitors, increasing epithelial cell density. p53-deficient progenitors generated a pseudostratified epithelium containing basal-like cells in vitro and putative bronchioalveolar stem cells in vivo. Conversely, an additional copy of p53 increased quiescence and ciliated cell differentiation, high-lighting the importance of tight regulation of p53 levels. Using single-cell RNA sequencing, we found that loss of p53 altered the molecular phenotype of progenitors and differentially modulated cell-cycle regulatory genes. Together, these findings reveal that p53 is an essential regulator of progenitor cell behavior, which shapes our understanding of stem cell quiescence during homeostasis and in cancer development.
引用
收藏
页码:2173 / 2182
页数:10
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