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Inhibitory Effect of Mesenchymal Stem Cell Co-Culture on Erythroid Differentiation of K562 Cells Compared to The Control Group
OBJECTIVE: Bone marrow mesenchymal stem cells (BMMSCs) reside in the bone marrow and control the process of hematopoiesis. They are an excellent instrument for regenerative treatment and co-culture with hematopoietic stem cells (HSCs). MATERIALS AND METHODS: In this experimental study, K562 cell lin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241509/ https://www.ncbi.nlm.nih.gov/pubmed/28367423 |
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author | Saleh, Mahshid Shamsasanjan, Karim Movassaghpour, Ali Akbari Akbarzadehlaleh, Parvin Molaeipour, Zahra |
author_facet | Saleh, Mahshid Shamsasanjan, Karim Movassaghpour, Ali Akbari Akbarzadehlaleh, Parvin Molaeipour, Zahra |
author_sort | Saleh, Mahshid |
collection | PubMed |
description | OBJECTIVE: Bone marrow mesenchymal stem cells (BMMSCs) reside in the bone marrow and control the process of hematopoiesis. They are an excellent instrument for regenerative treatment and co-culture with hematopoietic stem cells (HSCs). MATERIALS AND METHODS: In this experimental study, K562 cell lines were either treated with butyric acid and co-cultured with MSCs, or cultivated in a conditioned medium from MSCs plus butyric acid for erythroid differentiation. We used the trypan blue dye exclusion assay to determine cell counts and viability in each group. For each group, we separately assessed erythroid differentiation of the K562 cell line with Giemsa stain under light microscopy, expression of specific markers of erythroid cells by flowcytometry, and erythroidspecific gene expressions by real-time polymerase chain reaction (RT-PCR). RESULTS: There was enhandced erythroid differentiation of K562 cells with butyric acid compared to the K562 cell line co-cultured with MSCs and butyric acid. Erythroid differentiation of the K562 cell line cultivated in conditioned medium with butyric acid was higher than the K562 cell line co-cultured with MSCs and butyric acid, but less than K562 cell line treated with butyric acid only. CONCLUSION: Our results showed that MSCs significantly suppressed erythropoiesis. Therefore, MSCs would not be a suitable optimal treatment strategy for patients with erythroid leukemia. |
format | Online Article Text |
id | pubmed-5241509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-52415092017-04-01 Inhibitory Effect of Mesenchymal Stem Cell Co-Culture on Erythroid Differentiation of K562 Cells Compared to The Control Group Saleh, Mahshid Shamsasanjan, Karim Movassaghpour, Ali Akbari Akbarzadehlaleh, Parvin Molaeipour, Zahra Cell J Original Article OBJECTIVE: Bone marrow mesenchymal stem cells (BMMSCs) reside in the bone marrow and control the process of hematopoiesis. They are an excellent instrument for regenerative treatment and co-culture with hematopoietic stem cells (HSCs). MATERIALS AND METHODS: In this experimental study, K562 cell lines were either treated with butyric acid and co-cultured with MSCs, or cultivated in a conditioned medium from MSCs plus butyric acid for erythroid differentiation. We used the trypan blue dye exclusion assay to determine cell counts and viability in each group. For each group, we separately assessed erythroid differentiation of the K562 cell line with Giemsa stain under light microscopy, expression of specific markers of erythroid cells by flowcytometry, and erythroidspecific gene expressions by real-time polymerase chain reaction (RT-PCR). RESULTS: There was enhandced erythroid differentiation of K562 cells with butyric acid compared to the K562 cell line co-cultured with MSCs and butyric acid. Erythroid differentiation of the K562 cell line cultivated in conditioned medium with butyric acid was higher than the K562 cell line co-cultured with MSCs and butyric acid, but less than K562 cell line treated with butyric acid only. CONCLUSION: Our results showed that MSCs significantly suppressed erythropoiesis. Therefore, MSCs would not be a suitable optimal treatment strategy for patients with erythroid leukemia. Royan Institute 2017 2016-12-21 /pmc/articles/PMC5241509/ /pubmed/28367423 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Saleh, Mahshid Shamsasanjan, Karim Movassaghpour, Ali Akbari Akbarzadehlaleh, Parvin Molaeipour, Zahra Inhibitory Effect of Mesenchymal Stem Cell Co-Culture on Erythroid Differentiation of K562 Cells Compared to The Control Group |
title | Inhibitory Effect of Mesenchymal Stem Cell Co-Culture
on Erythroid Differentiation of K562 Cells
Compared to The Control Group |
title_full | Inhibitory Effect of Mesenchymal Stem Cell Co-Culture
on Erythroid Differentiation of K562 Cells
Compared to The Control Group |
title_fullStr | Inhibitory Effect of Mesenchymal Stem Cell Co-Culture
on Erythroid Differentiation of K562 Cells
Compared to The Control Group |
title_full_unstemmed | Inhibitory Effect of Mesenchymal Stem Cell Co-Culture
on Erythroid Differentiation of K562 Cells
Compared to The Control Group |
title_short | Inhibitory Effect of Mesenchymal Stem Cell Co-Culture
on Erythroid Differentiation of K562 Cells
Compared to The Control Group |
title_sort | inhibitory effect of mesenchymal stem cell co-culture
on erythroid differentiation of k562 cells
compared to the control group |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241509/ https://www.ncbi.nlm.nih.gov/pubmed/28367423 |
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