Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro

Craniofacial defects can cause morbidness. Adipose‐derived stem cells (ADSCs) have shown great promise for osteogeneration and vascularization; therefore cocultures of differentiated ADSCs are explored to increase bone and vessel formation. In this study, ADSCs were induced into osteogenic ADSCs (os...

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Veröffentlicht in:Journal of cellular physiology 2018-12, Vol.233 (12), p.9458-9472
Hauptverfasser: Yang, Huifang, Hong, Nanrui, Liu, Hsiaowei, Wang, Jieda, Li, Yan, Wu, Shuyi
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container_issue 12
container_start_page 9458
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creator Yang, Huifang
Hong, Nanrui
Liu, Hsiaowei
Wang, Jieda
Li, Yan
Wu, Shuyi
description Craniofacial defects can cause morbidness. Adipose‐derived stem cells (ADSCs) have shown great promise for osteogeneration and vascularization; therefore cocultures of differentiated ADSCs are explored to increase bone and vessel formation. In this study, ADSCs were induced into osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs (endo‐ADSCs) cells, which were then cocultured in variable proportions (os‐ADSCs/endo‐ADSCs = 2:1, 1:1, 1:2). The os‐ADSCs in a ratio of 1:1 expressed more ALP, RUNX2 and COL‐I, whereas VEGF, vWF and CD31 were upregulated in the endo‐ADSCs of this group. Next generation RNA sequencing (RNA‐seq) was performed to evaluate the molecular mechanisms of cocultured ADSCs. The os‐ADSCs and endo‐ADSCs interacted with each other during osteogenic and angiogenic differentiation, especially at the ratio of 1:1, and were regulated by vascular‐related genes, cell‐mediated genes, bone‐related genes and the transforming growth factor β signaling pathway (TGF‐β), mitogen‐activated protein kinase signaling pathway (MAPK) and wnt signaling pathway (Wnt). Angptl4, apoe, mmp3, bmp6, mmp13 and fgf18 were detected to be up‐regulated, and cxcl12 and wnt5a were down‐regulated. The results showed that the gene expression levels were consistent with that in RNA‐seq. The cells were then seeded into self‐assembling peptide RADA16‐I scaffolds as cocultures (1:1) and monocultures (ADSCs, os‐ADSCs, endo‐ADSCs). The results showed that the cells of all groups grew and proliferated well on the scaffolds, and the cocultured group exhibited better osteogeneration and vascularization. In conclusion, cocultured os‐ADSCs and endo‐ADSCs at the ratio of 1:1 showed strong osteogenic and angiogenic differentiation. There is a great potential for osteogenesis and vascularization by 3D culturing cells in a 1:1 ratio in self‐assembling peptide RADA16‐I scaffolds, which requires evaluation for bone regeneration in vivo. The objective of this study was to coculture osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs in three types of ratios and then compare the osteogenesis and angiogenesis effects, preliminarily exploring the best cocultured proportion that will be seeded in RADA16‐I. We performed the study was because there is limited research illustrating the interactions between cocultured os‐ADSCs and endothelial ADSCs.
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Adipose‐derived stem cells (ADSCs) have shown great promise for osteogeneration and vascularization; therefore cocultures of differentiated ADSCs are explored to increase bone and vessel formation. In this study, ADSCs were induced into osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs (endo‐ADSCs) cells, which were then cocultured in variable proportions (os‐ADSCs/endo‐ADSCs = 2:1, 1:1, 1:2). The os‐ADSCs in a ratio of 1:1 expressed more ALP, RUNX2 and COL‐I, whereas VEGF, vWF and CD31 were upregulated in the endo‐ADSCs of this group. Next generation RNA sequencing (RNA‐seq) was performed to evaluate the molecular mechanisms of cocultured ADSCs. The os‐ADSCs and endo‐ADSCs interacted with each other during osteogenic and angiogenic differentiation, especially at the ratio of 1:1, and were regulated by vascular‐related genes, cell‐mediated genes, bone‐related genes and the transforming growth factor β signaling pathway (TGF‐β), mitogen‐activated protein kinase signaling pathway (MAPK) and wnt signaling pathway (Wnt). Angptl4, apoe, mmp3, bmp6, mmp13 and fgf18 were detected to be up‐regulated, and cxcl12 and wnt5a were down‐regulated. The results showed that the gene expression levels were consistent with that in RNA‐seq. The cells were then seeded into self‐assembling peptide RADA16‐I scaffolds as cocultures (1:1) and monocultures (ADSCs, os‐ADSCs, endo‐ADSCs). The results showed that the cells of all groups grew and proliferated well on the scaffolds, and the cocultured group exhibited better osteogeneration and vascularization. In conclusion, cocultured os‐ADSCs and endo‐ADSCs at the ratio of 1:1 showed strong osteogenic and angiogenic differentiation. There is a great potential for osteogenesis and vascularization by 3D culturing cells in a 1:1 ratio in self‐assembling peptide RADA16‐I scaffolds, which requires evaluation for bone regeneration in vivo. The objective of this study was to coculture osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs in three types of ratios and then compare the osteogenesis and angiogenesis effects, preliminarily exploring the best cocultured proportion that will be seeded in RADA16‐I. We performed the study was because there is limited research illustrating the interactions between cocultured os‐ADSCs and endothelial ADSCs.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.26838</identifier><identifier>PMID: 29995982</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>adipose‐derived stem cells (ADSCs) ; Angiogenesis ; Apolipoprotein E ; Biocompatibility ; Biomedical materials ; Bone growth ; Bone morphogenetic protein 6 ; Cbfa-1 protein ; coculture ; Collagenase 3 ; CXCL12 protein ; Differentiation ; Fibroblast growth factor 18 ; Gene expression ; Gene sequencing ; Genes ; Growth factors ; Kinases ; MAP kinase ; Molecular modelling ; Monoculture ; osteogeneration ; Osteogenesis ; Protein kinase ; Proteins ; RADA16‐I ; Regeneration ; Regeneration (physiology) ; Ribonucleic acid ; RNA ; RNA sequencing (RNA‐seq) ; Scaffolds ; Signal transduction ; Signaling ; Stem cells ; Transforming growth factor ; Transforming growth factor-b ; Vascular endothelial growth factor ; Vascularization ; Wnt protein</subject><ispartof>Journal of cellular physiology, 2018-12, Vol.233 (12), p.9458-9472</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><rights>2018 The Authors. Journal of Cellular Physiology Published by Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4198-305d5662c643ca719f2d8424076fb21847a636fdd6f664400dba9487a0801ce93</citedby><cites>FETCH-LOGICAL-c4198-305d5662c643ca719f2d8424076fb21847a636fdd6f664400dba9487a0801ce93</cites><orcidid>0000-0001-7716-1249 ; 0000-0003-2753-0063 ; 0000-0003-1989-9397 ; 0000-0001-7995-0591 ; 0000-0002-0873-8195 ; 0000-0003-2012-6834</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcp.26838$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcp.26838$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29995982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Huifang</creatorcontrib><creatorcontrib>Hong, Nanrui</creatorcontrib><creatorcontrib>Liu, Hsiaowei</creatorcontrib><creatorcontrib>Wang, Jieda</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Wu, Shuyi</creatorcontrib><title>Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>Craniofacial defects can cause morbidness. Adipose‐derived stem cells (ADSCs) have shown great promise for osteogeneration and vascularization; therefore cocultures of differentiated ADSCs are explored to increase bone and vessel formation. In this study, ADSCs were induced into osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs (endo‐ADSCs) cells, which were then cocultured in variable proportions (os‐ADSCs/endo‐ADSCs = 2:1, 1:1, 1:2). The os‐ADSCs in a ratio of 1:1 expressed more ALP, RUNX2 and COL‐I, whereas VEGF, vWF and CD31 were upregulated in the endo‐ADSCs of this group. Next generation RNA sequencing (RNA‐seq) was performed to evaluate the molecular mechanisms of cocultured ADSCs. The os‐ADSCs and endo‐ADSCs interacted with each other during osteogenic and angiogenic differentiation, especially at the ratio of 1:1, and were regulated by vascular‐related genes, cell‐mediated genes, bone‐related genes and the transforming growth factor β signaling pathway (TGF‐β), mitogen‐activated protein kinase signaling pathway (MAPK) and wnt signaling pathway (Wnt). Angptl4, apoe, mmp3, bmp6, mmp13 and fgf18 were detected to be up‐regulated, and cxcl12 and wnt5a were down‐regulated. The results showed that the gene expression levels were consistent with that in RNA‐seq. The cells were then seeded into self‐assembling peptide RADA16‐I scaffolds as cocultures (1:1) and monocultures (ADSCs, os‐ADSCs, endo‐ADSCs). The results showed that the cells of all groups grew and proliferated well on the scaffolds, and the cocultured group exhibited better osteogeneration and vascularization. In conclusion, cocultured os‐ADSCs and endo‐ADSCs at the ratio of 1:1 showed strong osteogenic and angiogenic differentiation. There is a great potential for osteogenesis and vascularization by 3D culturing cells in a 1:1 ratio in self‐assembling peptide RADA16‐I scaffolds, which requires evaluation for bone regeneration in vivo. The objective of this study was to coculture osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs in three types of ratios and then compare the osteogenesis and angiogenesis effects, preliminarily exploring the best cocultured proportion that will be seeded in RADA16‐I. 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Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Huifang</au><au>Hong, Nanrui</au><au>Liu, Hsiaowei</au><au>Wang, Jieda</au><au>Li, Yan</au><au>Wu, Shuyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2018-12</date><risdate>2018</risdate><volume>233</volume><issue>12</issue><spage>9458</spage><epage>9472</epage><pages>9458-9472</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Craniofacial defects can cause morbidness. Adipose‐derived stem cells (ADSCs) have shown great promise for osteogeneration and vascularization; therefore cocultures of differentiated ADSCs are explored to increase bone and vessel formation. In this study, ADSCs were induced into osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs (endo‐ADSCs) cells, which were then cocultured in variable proportions (os‐ADSCs/endo‐ADSCs = 2:1, 1:1, 1:2). The os‐ADSCs in a ratio of 1:1 expressed more ALP, RUNX2 and COL‐I, whereas VEGF, vWF and CD31 were upregulated in the endo‐ADSCs of this group. Next generation RNA sequencing (RNA‐seq) was performed to evaluate the molecular mechanisms of cocultured ADSCs. The os‐ADSCs and endo‐ADSCs interacted with each other during osteogenic and angiogenic differentiation, especially at the ratio of 1:1, and were regulated by vascular‐related genes, cell‐mediated genes, bone‐related genes and the transforming growth factor β signaling pathway (TGF‐β), mitogen‐activated protein kinase signaling pathway (MAPK) and wnt signaling pathway (Wnt). Angptl4, apoe, mmp3, bmp6, mmp13 and fgf18 were detected to be up‐regulated, and cxcl12 and wnt5a were down‐regulated. The results showed that the gene expression levels were consistent with that in RNA‐seq. The cells were then seeded into self‐assembling peptide RADA16‐I scaffolds as cocultures (1:1) and monocultures (ADSCs, os‐ADSCs, endo‐ADSCs). The results showed that the cells of all groups grew and proliferated well on the scaffolds, and the cocultured group exhibited better osteogeneration and vascularization. In conclusion, cocultured os‐ADSCs and endo‐ADSCs at the ratio of 1:1 showed strong osteogenic and angiogenic differentiation. There is a great potential for osteogenesis and vascularization by 3D culturing cells in a 1:1 ratio in self‐assembling peptide RADA16‐I scaffolds, which requires evaluation for bone regeneration in vivo. The objective of this study was to coculture osteogenic ADSCs (os‐ADSCs) and endothelial ADSCs in three types of ratios and then compare the osteogenesis and angiogenesis effects, preliminarily exploring the best cocultured proportion that will be seeded in RADA16‐I. 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subjects adipose‐derived stem cells (ADSCs)
Angiogenesis
Apolipoprotein E
Biocompatibility
Biomedical materials
Bone growth
Bone morphogenetic protein 6
Cbfa-1 protein
coculture
Collagenase 3
CXCL12 protein
Differentiation
Fibroblast growth factor 18
Gene expression
Gene sequencing
Genes
Growth factors
Kinases
MAP kinase
Molecular modelling
Monoculture
osteogeneration
Osteogenesis
Protein kinase
Proteins
RADA16‐I
Regeneration
Regeneration (physiology)
Ribonucleic acid
RNA
RNA sequencing (RNA‐seq)
Scaffolds
Signal transduction
Signaling
Stem cells
Transforming growth factor
Transforming growth factor-b
Vascular endothelial growth factor
Vascularization
Wnt protein
title Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro
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