Mammalian endoreplication emerges to reveal a potential developmental timer

被引:60
作者
Gandarillas, Alberto [1 ,2 ]
Molinuevo, Rut [1 ]
Sanz-Gomez, Natalia [1 ]
机构
[1] Inst Invest Marques de Valdecilla IDIVAL, Cell Cycle Stem Cell Fate & Canc Lab, Santander, Spain
[2] INSERM, Montpellier, France
关键词
INDUCED DIFFERENTIATION CHECKPOINT; DAMAGE-INDUCED DIFFERENTIATION; DNA-DAMAGE; CELL-CYCLE; STEM-CELLS; HUMAN KERATINOCYTES; LIVER-REGENERATION; CANCER DEVELOPMENT; GENOTOXIC STRESS; ENDOREDUPLICATION;
D O I
10.1038/s41418-017-0040-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Among the most intriguing and relevant questions in physiology is how developing tissues correctly coordinate proliferation with differentiation. Endoreplication, in a broad sense, is a consequence of a cell division block in the presence of an active cell cycle, and it typically occurs as cells differentiate terminally to fulfill a specialised function. Until recently, endoreplication was thought to be a rare variation of the cell cycle in mammals, more common in invertebrates and plants. However, in the last years, endoreplication has been uncovered in various tissues in mammalian organisms, including human. A recent report showing that cells in the mammary gland become binucleate at lactation sheds new insight into the importance of mammalian polyploidisation. We here propose that endoreplication is a widespread phenomenon in mammalian developing tissues that results from an automatic, robust and simple self-limiting mechanism coordinating cell multiplication with differentiation. This mechanism might act as a developmental timer. The model has implications for homeostasis control and carcinogenesis.
引用
收藏
页码:471 / 476
页数:6
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