Neutral competition of stem cells is skewed by proliferative changes downstream of Hh and Hpo

被引:62
作者
Amoyel, Marc [1 ]
Simons, Benjamin D. [2 ,3 ,4 ]
Bach, Erika A. [1 ,5 ]
机构
[1] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10003 USA
[2] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
[3] Univ Cambridge, Wellcome Trust CRUK Gurdon Inst, Cambridge, England
[4] Univ Cambridge, Wellcome Trust Med Res Council, Cambridge Stem Cell Inst, Cambridge, England
[5] NYU, Sch Med, Helen L & Martin S Kimmel Ctr Stem Cell Biol, New York, NY USA
基金
英国工程与自然科学研究理事会; 英国惠康基金;
关键词
competition; Hedgehog; Hippo; stem cell; testis; SELF-RENEWAL; DROSOPHILA TESTIS; TUMOR-SUPPRESSOR; JAK/STAT PATHWAY; GERMLINE; NICHE; DIVISION; MAINTENANCE; GROWTH; HEDGEHOG;
D O I
10.15252/embj.201387500
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
Neutral competition, an emerging feature of stem cell homeostasis, posits that individual stem cells can be lost and replaced by their neighbors stochastically, resulting in chance dominance of a clone at the niche. A single stem cell with an oncogenic mutation could bias this process and clonally spread the mutation throughout the stem cell pool. The Drosophila testis provides an ideal system for testing this model. The niche supports two stem cell populations that compete for niche occupancy. Here, we show that cyst stem cells (CySCs) conform to the paradigm of neutral competition and that clonal deregulation of either the Hedgehog (Hh) or Hippo (Hpo) pathway allows a single CySC to colonize the niche. We find that the driving force behind such behavior is accelerated proliferation. Our results demonstrate that a single stem cell colonizes its niche through oncogenic mutation by co-opting an underlying homeostatic process.
引用
收藏
页码:2295 / 2313
页数:19
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