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miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors

BACKGROUND: MSC-NTF cells are Mesenchymal Stromal Cells (MSC) induced to express high levels of neurotrophic factors (NTFs) using a culture-medium based approach. MSC-NTF cells have been successfully studied in clinical trials for Amyotrophic Lateral Sclerosis (ALS) patients. MicroRNAs (miRNA) are s...

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Autores principales: Gothelf, Yael, Kaspi, Haggai, Abramov, Natalie, Aricha, Revital
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678806/
https://www.ncbi.nlm.nih.gov/pubmed/29116031
http://dx.doi.org/10.1186/s13287-017-0692-1
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author Gothelf, Yael
Kaspi, Haggai
Abramov, Natalie
Aricha, Revital
author_facet Gothelf, Yael
Kaspi, Haggai
Abramov, Natalie
Aricha, Revital
author_sort Gothelf, Yael
collection PubMed
description BACKGROUND: MSC-NTF cells are Mesenchymal Stromal Cells (MSC) induced to express high levels of neurotrophic factors (NTFs) using a culture-medium based approach. MSC-NTF cells have been successfully studied in clinical trials for Amyotrophic Lateral Sclerosis (ALS) patients. MicroRNAs (miRNA) are short non-coding RNA molecules that coordinate post-transcriptional regulation of multiple gene targets. The purpose of this study was to determine whether the miRNA profile could provide a tool for MSC-NTF cell characterization and to distinguish them from the matched MSC from which they are derived. METHODS: NTF secretion in the culture supernatant of MSC-NTF cells was evaluated by ELISA assays. The Agilent microarray miRNA platform was used for pairwise comparisons of MSC-NTF cells to MSC. The differentially expressed miRNAs and putative mRNA targets were validated using qPCR analyses. RESULTS: Principal component analysis revealed two distinct clusters based on cell type (MSC and MSC-NTFs). Nineteen miRNAs were found to be upregulated and 22 miRNAs were downregulated in MSC-NTF cells relative to the MSC cells of origin. Further validation of differentially expressed miRNAs confirmed that miR-3663 and miR-132 were increased 18.5- and 4.06-fold, respectively while hsa-miR-503 was reduced more than 15-fold, suggesting that miRNAs could form the basis of an MSC-NTF cell characterization assay. In an analysis of the miRNA mRNA targets, three mRNA targets of hsa-miR-132-3p (HN-1, RASA1 and KLH-L11) were found to be significantly downregulated. CONCLUSIONS: We have demonstrated that MSC-NTF cells can be distinguished from their MSCs of origin by a unique miRNA expression profile. TRIAL REGISTRATION: Clinicaltrial.gov identifier NCT01777646. Registered 12 December 2012.
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spelling pubmed-56788062017-11-17 miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors Gothelf, Yael Kaspi, Haggai Abramov, Natalie Aricha, Revital Stem Cell Res Ther Research BACKGROUND: MSC-NTF cells are Mesenchymal Stromal Cells (MSC) induced to express high levels of neurotrophic factors (NTFs) using a culture-medium based approach. MSC-NTF cells have been successfully studied in clinical trials for Amyotrophic Lateral Sclerosis (ALS) patients. MicroRNAs (miRNA) are short non-coding RNA molecules that coordinate post-transcriptional regulation of multiple gene targets. The purpose of this study was to determine whether the miRNA profile could provide a tool for MSC-NTF cell characterization and to distinguish them from the matched MSC from which they are derived. METHODS: NTF secretion in the culture supernatant of MSC-NTF cells was evaluated by ELISA assays. The Agilent microarray miRNA platform was used for pairwise comparisons of MSC-NTF cells to MSC. The differentially expressed miRNAs and putative mRNA targets were validated using qPCR analyses. RESULTS: Principal component analysis revealed two distinct clusters based on cell type (MSC and MSC-NTFs). Nineteen miRNAs were found to be upregulated and 22 miRNAs were downregulated in MSC-NTF cells relative to the MSC cells of origin. Further validation of differentially expressed miRNAs confirmed that miR-3663 and miR-132 were increased 18.5- and 4.06-fold, respectively while hsa-miR-503 was reduced more than 15-fold, suggesting that miRNAs could form the basis of an MSC-NTF cell characterization assay. In an analysis of the miRNA mRNA targets, three mRNA targets of hsa-miR-132-3p (HN-1, RASA1 and KLH-L11) were found to be significantly downregulated. CONCLUSIONS: We have demonstrated that MSC-NTF cells can be distinguished from their MSCs of origin by a unique miRNA expression profile. TRIAL REGISTRATION: Clinicaltrial.gov identifier NCT01777646. Registered 12 December 2012. BioMed Central 2017-11-07 /pmc/articles/PMC5678806/ /pubmed/29116031 http://dx.doi.org/10.1186/s13287-017-0692-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gothelf, Yael
Kaspi, Haggai
Abramov, Natalie
Aricha, Revital
miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title_full miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title_fullStr miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title_full_unstemmed miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title_short miRNA profiling of NurOwn®: mesenchymal stem cells secreting neurotrophic factors
title_sort mirna profiling of nurown®: mesenchymal stem cells secreting neurotrophic factors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678806/
https://www.ncbi.nlm.nih.gov/pubmed/29116031
http://dx.doi.org/10.1186/s13287-017-0692-1
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