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Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model

Studies of the normal functions and diseases of the prostate request in vivo models that maintain the tissue architecture and the multiple-cell type compartments of human origin in order to recapitulate reliably the interactions of different cell types. Cell type-specific transcriptomes are critical...

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Autores principales: Gross, Nelson T., Wang, Jianmin, Fiandalo, Michael V., Cortes Gomez, Eduardo, Watts, Anica, Godoy, Alejandro S., Smith, Gary J., Wu, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316257/
https://www.ncbi.nlm.nih.gov/pubmed/32584883
http://dx.doi.org/10.1371/journal.pone.0233899
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author Gross, Nelson T.
Wang, Jianmin
Fiandalo, Michael V.
Cortes Gomez, Eduardo
Watts, Anica
Godoy, Alejandro S.
Smith, Gary J.
Wu, Yue
author_facet Gross, Nelson T.
Wang, Jianmin
Fiandalo, Michael V.
Cortes Gomez, Eduardo
Watts, Anica
Godoy, Alejandro S.
Smith, Gary J.
Wu, Yue
author_sort Gross, Nelson T.
collection PubMed
description Studies of the normal functions and diseases of the prostate request in vivo models that maintain the tissue architecture and the multiple-cell type compartments of human origin in order to recapitulate reliably the interactions of different cell types. Cell type-specific transcriptomes are critical to reveal the roles of each cell type in the functions and diseases of the prostate. A primary prostate tissue xenograft model was developed using fresh human prostate tissue specimens transplanted onto male mice that were castrated surgically and implanted with a device to maintain circulating testosterone levels comparable to adult human males. Endothelial cells and epithelial cells were isolated from 7 fresh human prostate tissue specimens and from primary tissue xenografts established from 9 fresh human prostate tissue specimens, using antibody-conjugated magnetic beads specific to human CD31 and human EpCAM, respectively. Transcriptomes of endothelial, epithelial and stromal cell fractions were obtained using RNA-Seq. Global and function-specific gene expression profiles were compared in inter-cell type and inter-tissue type manners. Gene expression profiles in the individual cell types isolated from xenografts were similar to those of cells isolated from fresh tissue, demonstrating the value of the primary tissue xenograft model for studies of the inter-relationships between prostatic cell types and the role of such inter-relationships in organ development, disease progression, and response to drug treatments.
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spelling pubmed-73162572020-06-29 Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model Gross, Nelson T. Wang, Jianmin Fiandalo, Michael V. Cortes Gomez, Eduardo Watts, Anica Godoy, Alejandro S. Smith, Gary J. Wu, Yue PLoS One Research Article Studies of the normal functions and diseases of the prostate request in vivo models that maintain the tissue architecture and the multiple-cell type compartments of human origin in order to recapitulate reliably the interactions of different cell types. Cell type-specific transcriptomes are critical to reveal the roles of each cell type in the functions and diseases of the prostate. A primary prostate tissue xenograft model was developed using fresh human prostate tissue specimens transplanted onto male mice that were castrated surgically and implanted with a device to maintain circulating testosterone levels comparable to adult human males. Endothelial cells and epithelial cells were isolated from 7 fresh human prostate tissue specimens and from primary tissue xenografts established from 9 fresh human prostate tissue specimens, using antibody-conjugated magnetic beads specific to human CD31 and human EpCAM, respectively. Transcriptomes of endothelial, epithelial and stromal cell fractions were obtained using RNA-Seq. Global and function-specific gene expression profiles were compared in inter-cell type and inter-tissue type manners. Gene expression profiles in the individual cell types isolated from xenografts were similar to those of cells isolated from fresh tissue, demonstrating the value of the primary tissue xenograft model for studies of the inter-relationships between prostatic cell types and the role of such inter-relationships in organ development, disease progression, and response to drug treatments. Public Library of Science 2020-06-25 /pmc/articles/PMC7316257/ /pubmed/32584883 http://dx.doi.org/10.1371/journal.pone.0233899 Text en © 2020 Gross et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gross, Nelson T.
Wang, Jianmin
Fiandalo, Michael V.
Cortes Gomez, Eduardo
Watts, Anica
Godoy, Alejandro S.
Smith, Gary J.
Wu, Yue
Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title_full Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title_fullStr Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title_full_unstemmed Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title_short Recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
title_sort recapitulation of prostate tissue cell type-specific transcriptomes by an in vivo primary prostate tissue xenograft model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316257/
https://www.ncbi.nlm.nih.gov/pubmed/32584883
http://dx.doi.org/10.1371/journal.pone.0233899
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