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A molecular classification of human mesenchymal stromal cells

Mesenchymal stromal cells (MSC) are widely used for the study of mesenchymal tissue repair, and increasingly adopted for cell therapy, despite the lack of consensus on the identity of these cells. In part this is due to the lack of specificity of MSC markers. Distinguishing MSC from other stromal ce...

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Autores principales: Rohart, Florian, Mason, Elizabeth A., Matigian, Nicholas, Mosbergen, Rowland, Korn, Othmar, Chen, Tyrone, Butcher, Suzanne, Patel, Jatin, Atkinson, Kerry, Khosrotehrani, Kiarash, Fisk, Nicholas M., Lê Cao, Kim-Anh, Wells, Christine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811172/
https://www.ncbi.nlm.nih.gov/pubmed/27042394
http://dx.doi.org/10.7717/peerj.1845
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author Rohart, Florian
Mason, Elizabeth A.
Matigian, Nicholas
Mosbergen, Rowland
Korn, Othmar
Chen, Tyrone
Butcher, Suzanne
Patel, Jatin
Atkinson, Kerry
Khosrotehrani, Kiarash
Fisk, Nicholas M.
Lê Cao, Kim-Anh
Wells, Christine A.
author_facet Rohart, Florian
Mason, Elizabeth A.
Matigian, Nicholas
Mosbergen, Rowland
Korn, Othmar
Chen, Tyrone
Butcher, Suzanne
Patel, Jatin
Atkinson, Kerry
Khosrotehrani, Kiarash
Fisk, Nicholas M.
Lê Cao, Kim-Anh
Wells, Christine A.
author_sort Rohart, Florian
collection PubMed
description Mesenchymal stromal cells (MSC) are widely used for the study of mesenchymal tissue repair, and increasingly adopted for cell therapy, despite the lack of consensus on the identity of these cells. In part this is due to the lack of specificity of MSC markers. Distinguishing MSC from other stromal cells such as fibroblasts is particularly difficult using standard analysis of surface proteins, and there is an urgent need for improved classification approaches. Transcriptome profiling is commonly used to describe and compare different cell types; however, efforts to identify specific markers of rare cellular subsets may be confounded by the small sample sizes of most studies. Consequently, it is difficult to derive reproducible, and therefore useful markers. We addressed the question of MSC classification with a large integrative analysis of many public MSC datasets. We derived a sparse classifier (The Rohart MSC test) that accurately distinguished MSC from non-MSC samples with >97% accuracy on an internal training set of 635 samples from 41 studies derived on 10 different microarray platforms. The classifier was validated on an external test set of 1,291 samples from 65 studies derived on 15 different platforms, with >95% accuracy. The genes that contribute to the MSC classifier formed a protein-interaction network that included known MSC markers. Further evidence of the relevance of this new MSC panel came from the high number of Mendelian disorders associated with mutations in more than 65% of the network. These result in mesenchymal defects, particularly impacting on skeletal growth and function. The Rohart MSC test is a simple in silico test that accurately discriminates MSC from fibroblasts, other adult stem/progenitor cell types or differentiated stromal cells. It has been implemented in the www.stemformatics.org resource, to assist researchers wishing to benchmark their own MSC datasets or data from the public domain. The code is available from the CRAN repository and all data used to generate the MSC test is available to download via the Gene Expression Omnibus or the Stemformatics resource.
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spelling pubmed-48111722016-04-01 A molecular classification of human mesenchymal stromal cells Rohart, Florian Mason, Elizabeth A. Matigian, Nicholas Mosbergen, Rowland Korn, Othmar Chen, Tyrone Butcher, Suzanne Patel, Jatin Atkinson, Kerry Khosrotehrani, Kiarash Fisk, Nicholas M. Lê Cao, Kim-Anh Wells, Christine A. PeerJ Bioinformatics Mesenchymal stromal cells (MSC) are widely used for the study of mesenchymal tissue repair, and increasingly adopted for cell therapy, despite the lack of consensus on the identity of these cells. In part this is due to the lack of specificity of MSC markers. Distinguishing MSC from other stromal cells such as fibroblasts is particularly difficult using standard analysis of surface proteins, and there is an urgent need for improved classification approaches. Transcriptome profiling is commonly used to describe and compare different cell types; however, efforts to identify specific markers of rare cellular subsets may be confounded by the small sample sizes of most studies. Consequently, it is difficult to derive reproducible, and therefore useful markers. We addressed the question of MSC classification with a large integrative analysis of many public MSC datasets. We derived a sparse classifier (The Rohart MSC test) that accurately distinguished MSC from non-MSC samples with >97% accuracy on an internal training set of 635 samples from 41 studies derived on 10 different microarray platforms. The classifier was validated on an external test set of 1,291 samples from 65 studies derived on 15 different platforms, with >95% accuracy. The genes that contribute to the MSC classifier formed a protein-interaction network that included known MSC markers. Further evidence of the relevance of this new MSC panel came from the high number of Mendelian disorders associated with mutations in more than 65% of the network. These result in mesenchymal defects, particularly impacting on skeletal growth and function. The Rohart MSC test is a simple in silico test that accurately discriminates MSC from fibroblasts, other adult stem/progenitor cell types or differentiated stromal cells. It has been implemented in the www.stemformatics.org resource, to assist researchers wishing to benchmark their own MSC datasets or data from the public domain. The code is available from the CRAN repository and all data used to generate the MSC test is available to download via the Gene Expression Omnibus or the Stemformatics resource. PeerJ Inc. 2016-03-24 /pmc/articles/PMC4811172/ /pubmed/27042394 http://dx.doi.org/10.7717/peerj.1845 Text en ©2016 Rohart 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, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Rohart, Florian
Mason, Elizabeth A.
Matigian, Nicholas
Mosbergen, Rowland
Korn, Othmar
Chen, Tyrone
Butcher, Suzanne
Patel, Jatin
Atkinson, Kerry
Khosrotehrani, Kiarash
Fisk, Nicholas M.
Lê Cao, Kim-Anh
Wells, Christine A.
A molecular classification of human mesenchymal stromal cells
title A molecular classification of human mesenchymal stromal cells
title_full A molecular classification of human mesenchymal stromal cells
title_fullStr A molecular classification of human mesenchymal stromal cells
title_full_unstemmed A molecular classification of human mesenchymal stromal cells
title_short A molecular classification of human mesenchymal stromal cells
title_sort molecular classification of human mesenchymal stromal cells
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811172/
https://www.ncbi.nlm.nih.gov/pubmed/27042394
http://dx.doi.org/10.7717/peerj.1845
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