Increasing Neural Stem Cell Division Asymmetry and Quiescence Are Predicted to Contribute to the Age-Related Decline in Neurogenesis

被引:35
作者
Bast, Lisa [1 ,2 ]
Calzolari, Filippo [3 ,4 ,5 ]
Strasser, Michael K. [1 ,7 ]
Hasenauer, Jan [1 ,2 ]
Theis, Fabian J. [1 ,2 ]
Ninkovic, Jovica [4 ,5 ,6 ]
Marr, Carsten [1 ]
机构
[1] Helmholtz Zentrum Muunchen, Inst Computat Biol, German Res Ctr Environm Hlth, Neuherberg, Germany
[2] Tech Univ Munich, Dept Math, Chair Math Modeling Biol Syst, Garching, Germany
[3] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Physiol Chem, Mainz, Germany
[4] Helmholtz Zentrum Munchen, Inst Stem Cell Res, German Res Ctr Environm Hlth, Neuherberg, Germany
[5] Ludwig Maximilians Univ Munchen, Dept Physiol Genom, Munich, Germany
[6] Ludwig Maximilians Univ Munchen, Dept Cell Biol & Anat, Biomed Ctr LMU, Munich, Germany
[7] Inst Syst Biol, Seattle, WA USA
关键词
SUBVENTRICULAR ZONE; LINEAGE PROGRESSION; EMBRYONIC ORIGIN; PROGENITORS; DERIVATION; CRITERION; CYCLE; POOL;
D O I
10.1016/j.celrep.2018.11.088
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adult murine neural stem cells (NSCs) generate neurons in drastically declining numbers with age. How cellular dynamics sustain neurogenesis and how alterations with age may result in this decline are unresolved issues. We therefore clonally traced NSC lineages using confetti reporters in young and middle-aged adult mice. To understand the underlying mechanisms, we derived mathematical models that explain observed clonal cell type abundances. The best models consistently show self-renewal of transit-amplifying progenitors and rapid neuroblast cell cycle exit. In middle-aged mice, we identified an increased probability of asymmetric stem cell divisions at the expense of symmetric differentiation, accompanied by an extended persistence of quiescence between activation phases. Our model explains existing longitudinal population data and identifies particular cellular properties underlying adult NSC homeostasis and the aging of this stem cell compartment.
引用
收藏
页码:3231 / +
页数:18
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