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Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient

The aim of the present study was to investigate the morphological characteristics and pluripotent differentiation potential of human bone marrow mesenchymal stem cells (hBMMSCs) in vitro and in vivo. Bone marrow cells were isolated from a rib fragment of an adult surgical patient, hBMMSCs were isola...

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Autores principales: HUANG, JIA, SHA, HUIFAN, WANG, GUAN, BAO, GUOLIANG, LU, SHUN, LUO, QINGQUAN, TAN, QIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270342/
https://www.ncbi.nlm.nih.gov/pubmed/25376882
http://dx.doi.org/10.3892/mmr.2014.2892
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author HUANG, JIA
SHA, HUIFAN
WANG, GUAN
BAO, GUOLIANG
LU, SHUN
LUO, QINGQUAN
TAN, QIANG
author_facet HUANG, JIA
SHA, HUIFAN
WANG, GUAN
BAO, GUOLIANG
LU, SHUN
LUO, QINGQUAN
TAN, QIANG
author_sort HUANG, JIA
collection PubMed
description The aim of the present study was to investigate the morphological characteristics and pluripotent differentiation potential of human bone marrow mesenchymal stem cells (hBMMSCs) in vitro and in vivo. Bone marrow cells were isolated from a rib fragment of an adult surgical patient, hBMMSCs were isolated based on plastic adherence and expanded ex vivo and phenotyping was performed. Pluripotent differentiation assays for adipogenesis, myogenesis and osteogenesis were conducted. Hematopoietic reconstruction of sublethally irradiated nude mice was performed by infusion of hBMMSCs. The gene expression profiles of early and late hBMMSCs were examined. The rate of CD31-positive cells was 31.1% in passage (P)4 hBMMSCs and 18.6% in P10 hBMMSCs. CD105 and CD106 were expressed in 99 and 95% of P25 hBMMSCs, respectively. Lipid droplets appeared at day 18 post induction. For osteogenesis, palpable masses were grossly observed from day 35 post inoculation of hBMMSCs. Hematoxylin and eosin staining further revealed chondrocytes and bone tissues. For myogenesis, at day six post subcutaneous inoculation, hBMMSCs differentiated into myocytes and were positive for myoglobin and MyoD1. In irradiated nude mice reconstituted by hBMMSCs, the white blood cell count briefly decreased following irradiation; however, it gradually recovered. In the irradiated nude mice reconstituted with hBMMSCs, CD45- and CD34-positive cells were detected 72 h post induction. Gene microarray analysis of P7 and P57 hBMMSCs demonstrated that 20 genes were upregulated >2 fold and 40 genes were downregulated >2 fold in P57 hBMMSCs. In conclusion, the isolated HBMMSCs possessed pluripotent differentiation potential and it was feasible and safe to use hBMMSCs within 30 passages.
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spelling pubmed-42703422014-12-19 Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient HUANG, JIA SHA, HUIFAN WANG, GUAN BAO, GUOLIANG LU, SHUN LUO, QINGQUAN TAN, QIANG Mol Med Rep Articles The aim of the present study was to investigate the morphological characteristics and pluripotent differentiation potential of human bone marrow mesenchymal stem cells (hBMMSCs) in vitro and in vivo. Bone marrow cells were isolated from a rib fragment of an adult surgical patient, hBMMSCs were isolated based on plastic adherence and expanded ex vivo and phenotyping was performed. Pluripotent differentiation assays for adipogenesis, myogenesis and osteogenesis were conducted. Hematopoietic reconstruction of sublethally irradiated nude mice was performed by infusion of hBMMSCs. The gene expression profiles of early and late hBMMSCs were examined. The rate of CD31-positive cells was 31.1% in passage (P)4 hBMMSCs and 18.6% in P10 hBMMSCs. CD105 and CD106 were expressed in 99 and 95% of P25 hBMMSCs, respectively. Lipid droplets appeared at day 18 post induction. For osteogenesis, palpable masses were grossly observed from day 35 post inoculation of hBMMSCs. Hematoxylin and eosin staining further revealed chondrocytes and bone tissues. For myogenesis, at day six post subcutaneous inoculation, hBMMSCs differentiated into myocytes and were positive for myoglobin and MyoD1. In irradiated nude mice reconstituted by hBMMSCs, the white blood cell count briefly decreased following irradiation; however, it gradually recovered. In the irradiated nude mice reconstituted with hBMMSCs, CD45- and CD34-positive cells were detected 72 h post induction. Gene microarray analysis of P7 and P57 hBMMSCs demonstrated that 20 genes were upregulated >2 fold and 40 genes were downregulated >2 fold in P57 hBMMSCs. In conclusion, the isolated HBMMSCs possessed pluripotent differentiation potential and it was feasible and safe to use hBMMSCs within 30 passages. D.A. Spandidos 2015-03 2014-11-06 /pmc/articles/PMC4270342/ /pubmed/25376882 http://dx.doi.org/10.3892/mmr.2014.2892 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
HUANG, JIA
SHA, HUIFAN
WANG, GUAN
BAO, GUOLIANG
LU, SHUN
LUO, QINGQUAN
TAN, QIANG
Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title_full Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title_fullStr Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title_full_unstemmed Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title_short Isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
title_sort isolation and characterization of ex vivo expanded mesenchymal stem cells obtained from a surgical patient
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270342/
https://www.ncbi.nlm.nih.gov/pubmed/25376882
http://dx.doi.org/10.3892/mmr.2014.2892
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