p63 regulates commitment to the prostate cell lineage

被引:123
作者
Signoretti, S
Pires, MM
Lindauer, M
Horner, JW
Grisanzio, C
Dhar, S
Majumder, P
McKeon, F
Kantoff, PW
Sellers, WR
Loda, M [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[4] Harvard Univ, MIT, Broad Inst, Cambridge, MA 02141 USA
[5] Whitehead Inst Biomed Res, Cambridge, MA 02141 USA
关键词
animal model; development; stem cell; urothelium; mouse model;
D O I
10.1073/pnas.0500165102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular mechanisms underlying prostate and urothelial development remain unclear. This situation presents major limitations in identifying the cell type(s) and molecular events involved in the development of prostate and bladder cancer. It has been shown that mice lacking the basal cell marker p63 present several epithelial defects, including epidermis and prostate buds agenesis and urothelial abnormalities. Here, we use the p63-/- mouse as a tool to define cell lineages in the prostate epithelium and urothelium. By complementing p63(-/-) blastocysts with p63+/+ beta-galactosiclase (beta-gal)- positive ES cells, we show that secretory cells of the prostate originate from p63-positive basal progenitor cells. Importantly, our urogenital sinus transplantation studies demonstrate that p63 prevents intestinal differentiation of the urogenital sinus endoderm and is therefore required to maintain commitment to the prostate cell lineage. Finally, in contrast with the prostate findings, analysis of the urothelium from rescued p63-/- chimeras shows that umbrella (superficial) cells can develop and be maintained independently from p63-positive basal and intermediate cells.
引用
收藏
页码:11355 / 11360
页数:6
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