类有机物
生物
祖细胞
前列腺
细胞生物学
干细胞
基础(医学)
谱系标记
上皮
祖细胞
细胞分化
内分泌学
遗传学
基因
癌症
胰岛素
作者
Wouter R. Karthaus,Phillip J. Iaquinta,Jarno Drost,Ana Gudelj Gračanin,Ruben van Boxtel,John Wongvipat,Catherine Dowling,Dong Gao,Harry Begthel,Norman Sachs,Robert G.J. Vries,Edwin Cuppen,Yu Chen,Charles L. Sawyers,Hans Clevers
出处
期刊:Cell
[Cell Press]
日期:2014-09-01
卷期号:159 (1): 163-175
被引量:649
标识
DOI:10.1016/j.cell.2014.08.017
摘要
The prostate gland consists of basal and luminal cells arranged as pseudostratified epithelium. In tissue recombination models, only basal cells reconstitute a complete prostate gland, yet murine lineage-tracing experiments show that luminal cells generate basal cells. It has remained challenging to address the molecular details of these transitions and whether they apply to humans, due to the lack of culture conditions that recapitulate prostate gland architecture. Here, we describe a 3D culture system that supports long-term expansion of primary mouse and human prostate organoids, composed of fully differentiated CK5+ basal and CK8+ luminal cells. Organoids are genetically stable, reconstitute prostate glands in recombination assays, and can be experimentally manipulated. Single human luminal and basal cells give rise to organoids, yet luminal-cell-derived organoids more closely resemble prostate glands. These data support a luminal multilineage progenitor cell model for prostate tissue and establish a robust, scalable system for mechanistic studies.
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