Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency

Background: Derivation of induced pluripotent stem cells (iPSCs) from various adult somatic cells through over-expression of pluripotent genes could allow for the unlimited autologous supply in regenerative medicine. On the other hand the generation of various progenitors from bone-marrow mesenchyma...

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Main Author: T Foroutan
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2016-04-01
Series:International Journal of Organ Transplantation Medicine
Subjects:
Online Access:http://www.ijotm.com/ojs/index.php/IJOTM/article/view/296
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author T Foroutan
author_facet T Foroutan
author_sort T Foroutan
collection DOAJ
description Background: Derivation of induced pluripotent stem cells (iPSCs) from various adult somatic cells through over-expression of pluripotent genes could allow for the unlimited autologous supply in regenerative medicine. On the other hand the generation of various progenitors from bone-marrow mesenchymal stem cells (MSCs) is justly well established. Objective: In this study we compared the expression level of pluripotent genes oct4, c-myc, sox-2, nanog, klf4 and lin28 in iPSCs and MSCs derived from bone marrow. Also the potential of osteogenesis of iPSCs and bone-marrow MSCs were compared. Methods: We analyzed the expression level of oct4, sox-2, c-myc, klf4, nanog and lin28 genes in human MSCs derived from iPSCs and MSCs by cell culture and real-time PCR. Also the expression level of osteocalcin and osteopontin in both groups were evaluated. Results: We found that the expression of osteogenic markers in differentiated iPSCs to osteoblast were higher than bone-marrow MSCs. While the levels of pluripotency genes oct4, c-myc and klf4 in iPSCs were significantly (p<0.05) higher than bone-marrow MSCs, MSCs showed higher expression of sox-2, nanog and lin28 compared with iPSCs (p=NS). Conclusion: It seems that the higher expression of osteopontin and osteocalcin in MSCs compared to iPSCs may be due to other factors (besides pluripotency) required for differentiation of stem cells to osteoblast.
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spelling doaj.art-c377dc01eb624f65bf3bd99edeebb5df2022-12-22T00:25:12ZengShiraz University of Medical SciencesInternational Journal of Organ Transplantation Medicine2008-64822008-64902016-04-0172210Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> PluripotencyT Foroutan0Department of Animal Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, IranBackground: Derivation of induced pluripotent stem cells (iPSCs) from various adult somatic cells through over-expression of pluripotent genes could allow for the unlimited autologous supply in regenerative medicine. On the other hand the generation of various progenitors from bone-marrow mesenchymal stem cells (MSCs) is justly well established. Objective: In this study we compared the expression level of pluripotent genes oct4, c-myc, sox-2, nanog, klf4 and lin28 in iPSCs and MSCs derived from bone marrow. Also the potential of osteogenesis of iPSCs and bone-marrow MSCs were compared. Methods: We analyzed the expression level of oct4, sox-2, c-myc, klf4, nanog and lin28 genes in human MSCs derived from iPSCs and MSCs by cell culture and real-time PCR. Also the expression level of osteocalcin and osteopontin in both groups were evaluated. Results: We found that the expression of osteogenic markers in differentiated iPSCs to osteoblast were higher than bone-marrow MSCs. While the levels of pluripotency genes oct4, c-myc and klf4 in iPSCs were significantly (p<0.05) higher than bone-marrow MSCs, MSCs showed higher expression of sox-2, nanog and lin28 compared with iPSCs (p=NS). Conclusion: It seems that the higher expression of osteopontin and osteocalcin in MSCs compared to iPSCs may be due to other factors (besides pluripotency) required for differentiation of stem cells to osteoblast.http://www.ijotm.com/ojs/index.php/IJOTM/article/view/296Induced pluripotent stem cellsMesenchymal stromal cellsGene expression profilingOsteogenesisXite transcript, mouse [Supplementary Concept]Genes, mycsox2 protein, xenopus [Supplementary Concept]
spellingShingle T Foroutan
Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
International Journal of Organ Transplantation Medicine
Induced pluripotent stem cells
Mesenchymal stromal cells
Gene expression profiling
Osteogenesis
Xite transcript, mouse [Supplementary Concept]
Genes, myc
sox2 protein, xenopus [Supplementary Concept]
title Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
title_full Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
title_fullStr Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
title_full_unstemmed Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
title_short Comparison of Differentiation of Induced Pluripotent Stem Cells and Bone-Marrow Mesenchymal Stem Cells to Osteoblast: Osteogenesis <em>versus</em> Pluripotency
title_sort comparison of differentiation of induced pluripotent stem cells and bone marrow mesenchymal stem cells to osteoblast osteogenesis em versus em pluripotency
topic Induced pluripotent stem cells
Mesenchymal stromal cells
Gene expression profiling
Osteogenesis
Xite transcript, mouse [Supplementary Concept]
Genes, myc
sox2 protein, xenopus [Supplementary Concept]
url http://www.ijotm.com/ojs/index.php/IJOTM/article/view/296
work_keys_str_mv AT tforoutan comparisonofdifferentiationofinducedpluripotentstemcellsandbonemarrowmesenchymalstemcellstoosteoblastosteogenesisemversusempluripotency