| Literature DB >> 25201529 |
Wouter R Karthaus1, Phillip J Iaquinta2, Jarno Drost1, Ana Gracanin1, Ruben van Boxtel1, John Wongvipat2, Catherine M Dowling2, Dong Gao2, Harry Begthel1, Norman Sachs1, Robert G J Vries1, Edwin Cuppen1, Yu Chen2, Charles L Sawyers3, Hans C Clevers4.
Abstract
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.Entities:
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Year: 2014 PMID: 25201529 PMCID: PMC4772677 DOI: 10.1016/j.cell.2014.08.017
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582