MicroRNA expression in bone marrow-derived human multipotent Stromal cells

Abstract Background Multipotent stromal cells (MSCs) are being studied in the field of regenerative medicine for their multi-lineage differentiation and immunoregulatory capacity. MicroRNAs (miRNAs) are short non-coding RNAs that are responsible for regulating gene expression by targeting transcript...

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Main Authors: Ian H. Bellayr, Abhinav Kumar, Raj K. Puri
Format: Article
Language:English
Published: BMC 2017-08-01
Series:BMC Genomics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12864-017-3997-7
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author Ian H. Bellayr
Abhinav Kumar
Raj K. Puri
author_facet Ian H. Bellayr
Abhinav Kumar
Raj K. Puri
author_sort Ian H. Bellayr
collection DOAJ
description Abstract Background Multipotent stromal cells (MSCs) are being studied in the field of regenerative medicine for their multi-lineage differentiation and immunoregulatory capacity. MicroRNAs (miRNAs) are short non-coding RNAs that are responsible for regulating gene expression by targeting transcripts, which can impact MSC functions such as cellular proliferation, differentiation, migration and cell death. miRNAs are expressed in MSCs; however, the impact of miRNAs on cellular functions and donor variability is not well understood. Eight MSC lines were expanded to passages 3, 5 and 7, and their miRNA expression was evaluated using microarray technology. Results Statistical analyses of our data revealed that 71 miRNAs out of 939 examined were expressed by this set of MSC lines at all passages and the expression of 11 miRNAs were significantly different between passages 3 and 7, while the expression of 7 miRNAs was significantly different between passages 3 and 5. The expression of these identified miRNAs was evaluated using RT-qPCR for both the first set of MSC lines (n = 6) and a second set of MSC lines (n = 7) expanded from passages 4 to 8. By RT-qPCR only 2 miRNAs, miR-638 and miR-572 were upregulated at passage 7 compared to passage 3 in the first set of MSC lines by 1.71 and 1.54 fold, respectively; and upregulated at passage 8 compared to passage 4 in the second set of MSC lines, 1.35 and 1.59 fold, respectively. Conclusions The expression of miR-638 and miR-572 can distinguish MSCs from two different passages of cell culture. These results may be useful in establishing critical quality attributes of MSCs and determining whether changes in these two miRNAs impact cellular functions.
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spelling doaj.art-8f6bd91f076745ef99795e9c7e562cb72022-12-21T23:11:41ZengBMCBMC Genomics1471-21642017-08-0118111310.1186/s12864-017-3997-7MicroRNA expression in bone marrow-derived human multipotent Stromal cellsIan H. Bellayr0Abhinav Kumar1Raj K. Puri2Tumor Vaccines and Biotechnology Branch, Division of Cellular and Gene Therapies, Center for Biologics and Evaluation Research, US Food and Drug AdministrationTumor Vaccines and Biotechnology Branch, Division of Cellular and Gene Therapies, Center for Biologics and Evaluation Research, US Food and Drug AdministrationTumor Vaccines and Biotechnology Branch, Division of Cellular and Gene Therapies, Center for Biologics and Evaluation Research, US Food and Drug AdministrationAbstract Background Multipotent stromal cells (MSCs) are being studied in the field of regenerative medicine for their multi-lineage differentiation and immunoregulatory capacity. MicroRNAs (miRNAs) are short non-coding RNAs that are responsible for regulating gene expression by targeting transcripts, which can impact MSC functions such as cellular proliferation, differentiation, migration and cell death. miRNAs are expressed in MSCs; however, the impact of miRNAs on cellular functions and donor variability is not well understood. Eight MSC lines were expanded to passages 3, 5 and 7, and their miRNA expression was evaluated using microarray technology. Results Statistical analyses of our data revealed that 71 miRNAs out of 939 examined were expressed by this set of MSC lines at all passages and the expression of 11 miRNAs were significantly different between passages 3 and 7, while the expression of 7 miRNAs was significantly different between passages 3 and 5. The expression of these identified miRNAs was evaluated using RT-qPCR for both the first set of MSC lines (n = 6) and a second set of MSC lines (n = 7) expanded from passages 4 to 8. By RT-qPCR only 2 miRNAs, miR-638 and miR-572 were upregulated at passage 7 compared to passage 3 in the first set of MSC lines by 1.71 and 1.54 fold, respectively; and upregulated at passage 8 compared to passage 4 in the second set of MSC lines, 1.35 and 1.59 fold, respectively. Conclusions The expression of miR-638 and miR-572 can distinguish MSCs from two different passages of cell culture. These results may be useful in establishing critical quality attributes of MSCs and determining whether changes in these two miRNAs impact cellular functions.http://link.springer.com/article/10.1186/s12864-017-3997-7Multipotent Stromal cellsMicroRNA expressionMicroarray
spellingShingle Ian H. Bellayr
Abhinav Kumar
Raj K. Puri
MicroRNA expression in bone marrow-derived human multipotent Stromal cells
BMC Genomics
Multipotent Stromal cells
MicroRNA expression
Microarray
title MicroRNA expression in bone marrow-derived human multipotent Stromal cells
title_full MicroRNA expression in bone marrow-derived human multipotent Stromal cells
title_fullStr MicroRNA expression in bone marrow-derived human multipotent Stromal cells
title_full_unstemmed MicroRNA expression in bone marrow-derived human multipotent Stromal cells
title_short MicroRNA expression in bone marrow-derived human multipotent Stromal cells
title_sort microrna expression in bone marrow derived human multipotent stromal cells
topic Multipotent Stromal cells
MicroRNA expression
Microarray
url http://link.springer.com/article/10.1186/s12864-017-3997-7
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AT abhinavkumar micrornaexpressioninbonemarrowderivedhumanmultipotentstromalcells
AT rajkpuri micrornaexpressioninbonemarrowderivedhumanmultipotentstromalcells