Single luminal epithelial progenitors can generate prostate organoids in culture
The intrinsic ability to exhibit self-organizing morphogenetic properties in ex vivo culture may represent a general property of tissue stem cells. Here we show that single luminal stem/progenitor cells can generate prostate organoids in a three-dimensional culture system in the absence of stroma. O...
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Veröffentlicht in: | Nature cell biology 2014-10, Vol.16 (10), p.951-961 |
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creator | Chua, Chee Wai Shibata, Maho Lei, Ming Toivanen, Roxanne Barlow, LaMont J. Bergren, Sarah K. Badani, Ketan K. McKiernan, James M. Benson, Mitchell C. Hibshoosh, Hanina Shen, Michael M. |
description | The intrinsic ability to exhibit self-organizing morphogenetic properties in
ex vivo
culture may represent a general property of tissue stem cells. Here we show that single luminal stem/progenitor cells can generate prostate organoids in a three-dimensional culture system in the absence of stroma. Organoids generated from CARNs (castration-resistant Nkx3.1-expressing cells) or normal prostate epithelia exhibit tissue architecture containing luminal and basal cells, undergo long-term expansion in culture and exhibit functional androgen receptor signalling. Lineage-tracing demonstrates that luminal cells are favoured for organoid formation and generate basal cells in culture. Furthermore, tumour organoids can initiate from CARNs after oncogenic transformation and from mouse models of prostate cancer, and can facilitate analyses of drug response. Finally, we provide evidence supporting the feasibility of organoid studies of human prostate tissue. Our studies underscore the progenitor properties of luminal cells, and identify
in vitro
approaches for studying prostate biology.
Shen and colleagues report the
in vitro
generation of organoids from mouse luminal epithelial progenitor cells and normal or transformed prostate tissue, and extend this approach to the formation of normal and tumour organoids of human origin |
doi_str_mv | 10.1038/ncb3047 |
format | Article |
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ex vivo
culture may represent a general property of tissue stem cells. Here we show that single luminal stem/progenitor cells can generate prostate organoids in a three-dimensional culture system in the absence of stroma. Organoids generated from CARNs (castration-resistant Nkx3.1-expressing cells) or normal prostate epithelia exhibit tissue architecture containing luminal and basal cells, undergo long-term expansion in culture and exhibit functional androgen receptor signalling. Lineage-tracing demonstrates that luminal cells are favoured for organoid formation and generate basal cells in culture. Furthermore, tumour organoids can initiate from CARNs after oncogenic transformation and from mouse models of prostate cancer, and can facilitate analyses of drug response. Finally, we provide evidence supporting the feasibility of organoid studies of human prostate tissue. Our studies underscore the progenitor properties of luminal cells, and identify
in vitro
approaches for studying prostate biology.
Shen and colleagues report the
in vitro
generation of organoids from mouse luminal epithelial progenitor cells and normal or transformed prostate tissue, and extend this approach to the formation of normal and tumour organoids of human origin</description><identifier>ISSN: 1465-7392</identifier><identifier>EISSN: 1476-4679</identifier><identifier>DOI: 10.1038/ncb3047</identifier><identifier>PMID: 25241035</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 13/106 ; 13/31 ; 14/1 ; 14/19 ; 631/136/142 ; 631/532 ; 631/67/70 ; 64/60 ; Androgens ; Animals ; Biology ; Cancer Research ; Cell Biology ; Cell culture ; Cell Culture Techniques ; Cell Line, Tumor ; Cell Lineage ; Cells, Cultured ; Developmental Biology ; Epithelial Cells - cytology ; Epithelial Cells - metabolism ; Flow Cytometry ; Genetic aspects ; Homeodomain Proteins - metabolism ; Humans ; Innovations ; Life Sciences ; Luminescent Proteins - genetics ; Luminescent Proteins - metabolism ; Male ; Methods ; Mice, 129 Strain ; Mice, Inbred C57BL ; Mice, Transgenic ; Microscopy, Fluorescence ; Organoids - cytology ; Organoids - metabolism ; Phenotype ; Properties ; Prostate ; Prostate - cytology ; Prostate - metabolism ; Prostate cancer ; Prostatic Neoplasms, Castration-Resistant - metabolism ; Prostatic Neoplasms, Castration-Resistant - pathology ; Single-Cell Analysis - methods ; Stem Cells ; Stem Cells - cytology ; Stem Cells - metabolism ; Surgeons ; Time Factors ; Tissues ; Transcription Factors - metabolism ; University colleges</subject><ispartof>Nature cell biology, 2014-10, Vol.16 (10), p.951-961</ispartof><rights>Springer Nature Limited 2014</rights><rights>COPYRIGHT 2014 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Oct 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c597t-cefca39fd6a3b223c28bb9754174fa583652eb883c1508fe76c24892ae5454903</citedby><cites>FETCH-LOGICAL-c597t-cefca39fd6a3b223c28bb9754174fa583652eb883c1508fe76c24892ae5454903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ncb3047$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ncb3047$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25241035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chua, Chee Wai</creatorcontrib><creatorcontrib>Shibata, Maho</creatorcontrib><creatorcontrib>Lei, Ming</creatorcontrib><creatorcontrib>Toivanen, Roxanne</creatorcontrib><creatorcontrib>Barlow, LaMont J.</creatorcontrib><creatorcontrib>Bergren, Sarah K.</creatorcontrib><creatorcontrib>Badani, Ketan K.</creatorcontrib><creatorcontrib>McKiernan, James M.</creatorcontrib><creatorcontrib>Benson, Mitchell C.</creatorcontrib><creatorcontrib>Hibshoosh, Hanina</creatorcontrib><creatorcontrib>Shen, Michael M.</creatorcontrib><title>Single luminal epithelial progenitors can generate prostate organoids in culture</title><title>Nature cell biology</title><addtitle>Nat Cell Biol</addtitle><addtitle>Nat Cell Biol</addtitle><description>The intrinsic ability to exhibit self-organizing morphogenetic properties in
ex vivo
culture may represent a general property of tissue stem cells. Here we show that single luminal stem/progenitor cells can generate prostate organoids in a three-dimensional culture system in the absence of stroma. Organoids generated from CARNs (castration-resistant Nkx3.1-expressing cells) or normal prostate epithelia exhibit tissue architecture containing luminal and basal cells, undergo long-term expansion in culture and exhibit functional androgen receptor signalling. Lineage-tracing demonstrates that luminal cells are favoured for organoid formation and generate basal cells in culture. Furthermore, tumour organoids can initiate from CARNs after oncogenic transformation and from mouse models of prostate cancer, and can facilitate analyses of drug response. Finally, we provide evidence supporting the feasibility of organoid studies of human prostate tissue. Our studies underscore the progenitor properties of luminal cells, and identify
in vitro
approaches for studying prostate biology.
Shen and colleagues report the
in vitro
generation of organoids from mouse luminal epithelial progenitor cells and normal or transformed prostate tissue, and extend this approach to the formation of normal and tumour organoids of human origin</description><subject>13/100</subject><subject>13/106</subject><subject>13/31</subject><subject>14/1</subject><subject>14/19</subject><subject>631/136/142</subject><subject>631/532</subject><subject>631/67/70</subject><subject>64/60</subject><subject>Androgens</subject><subject>Animals</subject><subject>Biology</subject><subject>Cancer Research</subject><subject>Cell Biology</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Cell Line, Tumor</subject><subject>Cell Lineage</subject><subject>Cells, Cultured</subject><subject>Developmental Biology</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - metabolism</subject><subject>Flow Cytometry</subject><subject>Genetic aspects</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Humans</subject><subject>Innovations</subject><subject>Life Sciences</subject><subject>Luminescent Proteins - 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cytology</topic><topic>Epithelial Cells - metabolism</topic><topic>Flow Cytometry</topic><topic>Genetic aspects</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Humans</topic><topic>Innovations</topic><topic>Life Sciences</topic><topic>Luminescent Proteins - genetics</topic><topic>Luminescent Proteins - metabolism</topic><topic>Male</topic><topic>Methods</topic><topic>Mice, 129 Strain</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Microscopy, Fluorescence</topic><topic>Organoids - cytology</topic><topic>Organoids - metabolism</topic><topic>Phenotype</topic><topic>Properties</topic><topic>Prostate</topic><topic>Prostate - cytology</topic><topic>Prostate - metabolism</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms, Castration-Resistant - metabolism</topic><topic>Prostatic Neoplasms, Castration-Resistant - pathology</topic><topic>Single-Cell Analysis - methods</topic><topic>Stem Cells</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chua, Chee Wai</au><au>Shibata, Maho</au><au>Lei, Ming</au><au>Toivanen, Roxanne</au><au>Barlow, LaMont J.</au><au>Bergren, Sarah K.</au><au>Badani, Ketan K.</au><au>McKiernan, James M.</au><au>Benson, Mitchell C.</au><au>Hibshoosh, Hanina</au><au>Shen, Michael M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single luminal epithelial progenitors can generate prostate organoids in culture</atitle><jtitle>Nature cell biology</jtitle><stitle>Nat Cell Biol</stitle><addtitle>Nat Cell Biol</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>16</volume><issue>10</issue><spage>951</spage><epage>961</epage><pages>951-961</pages><issn>1465-7392</issn><eissn>1476-4679</eissn><abstract>The intrinsic ability to exhibit self-organizing morphogenetic properties in
ex vivo
culture may represent a general property of tissue stem cells. Here we show that single luminal stem/progenitor cells can generate prostate organoids in a three-dimensional culture system in the absence of stroma. Organoids generated from CARNs (castration-resistant Nkx3.1-expressing cells) or normal prostate epithelia exhibit tissue architecture containing luminal and basal cells, undergo long-term expansion in culture and exhibit functional androgen receptor signalling. Lineage-tracing demonstrates that luminal cells are favoured for organoid formation and generate basal cells in culture. Furthermore, tumour organoids can initiate from CARNs after oncogenic transformation and from mouse models of prostate cancer, and can facilitate analyses of drug response. Finally, we provide evidence supporting the feasibility of organoid studies of human prostate tissue. Our studies underscore the progenitor properties of luminal cells, and identify
in vitro
approaches for studying prostate biology.
Shen and colleagues report the
in vitro
generation of organoids from mouse luminal epithelial progenitor cells and normal or transformed prostate tissue, and extend this approach to the formation of normal and tumour organoids of human origin</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25241035</pmid><doi>10.1038/ncb3047</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/100 13/106 13/31 14/1 14/19 631/136/142 631/532 631/67/70 64/60 Androgens Animals Biology Cancer Research Cell Biology Cell culture Cell Culture Techniques Cell Line, Tumor Cell Lineage Cells, Cultured Developmental Biology Epithelial Cells - cytology Epithelial Cells - metabolism Flow Cytometry Genetic aspects Homeodomain Proteins - metabolism Humans Innovations Life Sciences Luminescent Proteins - genetics Luminescent Proteins - metabolism Male Methods Mice, 129 Strain Mice, Inbred C57BL Mice, Transgenic Microscopy, Fluorescence Organoids - cytology Organoids - metabolism Phenotype Properties Prostate Prostate - cytology Prostate - metabolism Prostate cancer Prostatic Neoplasms, Castration-Resistant - metabolism Prostatic Neoplasms, Castration-Resistant - pathology Single-Cell Analysis - methods Stem Cells Stem Cells - cytology Stem Cells - metabolism Surgeons Time Factors Tissues Transcription Factors - metabolism University colleges |
title | Single luminal epithelial progenitors can generate prostate organoids in culture |
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