Tuberous sclerosis complex and Myc coordinate the growth and division of Drosophila intestinal stem cells

被引:76
作者
Amcheslavsky, Alla [1 ]
Ito, Naoto [1 ]
Jiang, Jin [4 ,5 ]
Ip, Y. Tony [1 ,2 ,3 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Program Cell Dynam, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01605 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Dev Biol, Dallas, TX 75390 USA
[5] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
DNA-DAMAGE CHECKPOINT; CONTROLS SELF-RENEWAL; BACTERIAL-INFECTION; MULTIPLE PATHWAYS; TUMOR SUPPRESSORS; MTOR COMPLEX; IN-VIVO; PROLIFERATION; MIDGUT; DIFFERENTIATION;
D O I
10.1083/jcb.201103018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intestinal stem cells (ISCs) in the adult Drosophila melanogaster midgut can respond to damage and support repair. We demonstrate in this paper that the tuberous sclerosis complex (TSC) plays a critical role in balancing ISC growth and division. Previous studies have shown that imaginal disc cells that are mutant for TSC have increased rates of growth and division. However, we report in this paper that loss of TSC in the adult Drosophila midgut results in the formation of much larger ISCs that have halted cell division. These mutant ISCs expressed proper stem cell markers, did not differentiate, and had defects in multiple steps of the cell cycle. Slowing the growth by feeding rapamycin or reducing Myc was sufficient to rescue the division defect. The TSC mutant guts had a thinner epithelial structure than wild-type tissues, and the mutant flies were more susceptible to tissue damage. Therefore, we have uncovered a context-dependent phenotype of TSC mutants in adult ISCs, such that the excessive growth leads to inhibition of division.
引用
收藏
页码:695 / 710
页数:16
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