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...
Gespeichert in:
Veröffentlicht in: | Journal of cellular physiology 2018-12, Vol.233 (12), p.9458-9472 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 9472 |
---|---|
container_issue | 12 |
container_start_page | 9458 |
container_title | Journal of cellular physiology |
container_volume | 233 |
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. |
doi_str_mv | 10.1002/jcp.26838 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2068912925</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2068912925</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4198-305d5662c643ca719f2d8424076fb21847a636fdd6f664400dba9487a0801ce93</originalsourceid><addsrcrecordid>eNp1kE1OHDEQhS0UBBPCgguglrIhiwb_tdtejoaEgJBAUbK23HYZedTTntjdIHY5Qs7ISfAwhEUkVqWq-urV00PoiOBTgjE9W9r1KRWSyR00I1i1NRcN_YBmZUdq1XCyjz7mvMQYK8XYHtqnSqlGSTpD3XnwHhIMYzAjuMq4sI4Znv78dZDCfZnkEVaVhb6vbLRTP04JcuVjqro4QJXgDgZIZgxxqMJQ_Zifz4ko55eb7j6MKX5Cu970GQ5f6wH69e3rz8X3-vrm4nIxv64tJ0rWDDeuEYJawZk1LVGeOskpx63wHSWSt0Yw4Z0TXgjOMXadUVy2BktMLCh2gE62uusUf0-QR70KeWPcDBCnrCkWUhGqaFPQz_-hyzilobjTlJRXrG0YLdSXLWVTzDmB1-sUViY9aoL1JnhdgtcvwRf2-FVx6lbg3sh_SRfgbAs8hB4e31fSV4vbreQzJ5WM2g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2118437532</pqid></control><display><type>article</type><title>Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro</title><source>Wiley Online Library</source><creator>Yang, Huifang ; Hong, Nanrui ; Liu, Hsiaowei ; Wang, Jieda ; Li, Yan ; Wu, Shuyi</creator><creatorcontrib>Yang, Huifang ; Hong, Nanrui ; Liu, Hsiaowei ; Wang, Jieda ; Li, Yan ; Wu, Shuyi</creatorcontrib><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.</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. We performed the study was because there is limited research illustrating the interactions between cocultured os‐ADSCs and endothelial ADSCs.</description><subject>adipose‐derived stem cells (ADSCs)</subject><subject>Angiogenesis</subject><subject>Apolipoprotein E</subject><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Bone growth</subject><subject>Bone morphogenetic protein 6</subject><subject>Cbfa-1 protein</subject><subject>coculture</subject><subject>Collagenase 3</subject><subject>CXCL12 protein</subject><subject>Differentiation</subject><subject>Fibroblast growth factor 18</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Growth factors</subject><subject>Kinases</subject><subject>MAP kinase</subject><subject>Molecular modelling</subject><subject>Monoculture</subject><subject>osteogeneration</subject><subject>Osteogenesis</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>RADA16‐I</subject><subject>Regeneration</subject><subject>Regeneration (physiology)</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA sequencing (RNA‐seq)</subject><subject>Scaffolds</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Stem cells</subject><subject>Transforming growth factor</subject><subject>Transforming growth factor-b</subject><subject>Vascular endothelial growth factor</subject><subject>Vascularization</subject><subject>Wnt protein</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE1OHDEQhS0UBBPCgguglrIhiwb_tdtejoaEgJBAUbK23HYZedTTntjdIHY5Qs7ISfAwhEUkVqWq-urV00PoiOBTgjE9W9r1KRWSyR00I1i1NRcN_YBmZUdq1XCyjz7mvMQYK8XYHtqnSqlGSTpD3XnwHhIMYzAjuMq4sI4Znv78dZDCfZnkEVaVhb6vbLRTP04JcuVjqro4QJXgDgZIZgxxqMJQ_Zifz4ko55eb7j6MKX5Cu970GQ5f6wH69e3rz8X3-vrm4nIxv64tJ0rWDDeuEYJawZk1LVGeOskpx63wHSWSt0Yw4Z0TXgjOMXadUVy2BktMLCh2gE62uusUf0-QR70KeWPcDBCnrCkWUhGqaFPQz_-hyzilobjTlJRXrG0YLdSXLWVTzDmB1-sUViY9aoL1JnhdgtcvwRf2-FVx6lbg3sh_SRfgbAs8hB4e31fSV4vbreQzJ5WM2g</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Yang, Huifang</creator><creator>Hong, Nanrui</creator><creator>Liu, Hsiaowei</creator><creator>Wang, Jieda</creator><creator>Li, Yan</creator><creator>Wu, Shuyi</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7716-1249</orcidid><orcidid>https://orcid.org/0000-0003-2753-0063</orcidid><orcidid>https://orcid.org/0000-0003-1989-9397</orcidid><orcidid>https://orcid.org/0000-0001-7995-0591</orcidid><orcidid>https://orcid.org/0000-0002-0873-8195</orcidid><orcidid>https://orcid.org/0000-0003-2012-6834</orcidid></search><sort><creationdate>201812</creationdate><title>Differentiated adipose‐derived stem cell cocultures for bone regeneration in RADA16‐I in vitro</title><author>Yang, Huifang ; Hong, Nanrui ; Liu, Hsiaowei ; Wang, Jieda ; Li, Yan ; Wu, Shuyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4198-305d5662c643ca719f2d8424076fb21847a636fdd6f664400dba9487a0801ce93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>adipose‐derived stem cells (ADSCs)</topic><topic>Angiogenesis</topic><topic>Apolipoprotein E</topic><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Bone growth</topic><topic>Bone morphogenetic protein 6</topic><topic>Cbfa-1 protein</topic><topic>coculture</topic><topic>Collagenase 3</topic><topic>CXCL12 protein</topic><topic>Differentiation</topic><topic>Fibroblast growth factor 18</topic><topic>Gene expression</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Growth factors</topic><topic>Kinases</topic><topic>MAP kinase</topic><topic>Molecular modelling</topic><topic>Monoculture</topic><topic>osteogeneration</topic><topic>Osteogenesis</topic><topic>Protein kinase</topic><topic>Proteins</topic><topic>RADA16‐I</topic><topic>Regeneration</topic><topic>Regeneration (physiology)</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA sequencing (RNA‐seq)</topic><topic>Scaffolds</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Stem cells</topic><topic>Transforming growth factor</topic><topic>Transforming growth factor-b</topic><topic>Vascular endothelial growth factor</topic><topic>Vascularization</topic><topic>Wnt protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Huifang</creatorcontrib><creatorcontrib>Hong, Nanrui</creatorcontrib><creatorcontrib>Liu, Hsiaowei</creatorcontrib><creatorcontrib>Wang, Jieda</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Wu, Shuyi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & 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. We performed the study was because there is limited research illustrating the interactions between cocultured os‐ADSCs and endothelial ADSCs.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29995982</pmid><doi>10.1002/jcp.26838</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-7716-1249</orcidid><orcidid>https://orcid.org/0000-0003-2753-0063</orcidid><orcidid>https://orcid.org/0000-0003-1989-9397</orcidid><orcidid>https://orcid.org/0000-0001-7995-0591</orcidid><orcidid>https://orcid.org/0000-0002-0873-8195</orcidid><orcidid>https://orcid.org/0000-0003-2012-6834</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9541 |
ispartof | Journal of cellular physiology, 2018-12, Vol.233 (12), p.9458-9472 |
issn | 0021-9541 1097-4652 |
language | eng |
recordid | cdi_proquest_miscellaneous_2068912925 |
source | Wiley Online Library |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T19%3A11%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differentiated%20adipose%E2%80%90derived%20stem%20cell%20cocultures%20for%20bone%20regeneration%20in%20RADA16%E2%80%90I%20in%20vitro&rft.jtitle=Journal%20of%20cellular%20physiology&rft.au=Yang,%20Huifang&rft.date=2018-12&rft.volume=233&rft.issue=12&rft.spage=9458&rft.epage=9472&rft.pages=9458-9472&rft.issn=0021-9541&rft.eissn=1097-4652&rft_id=info:doi/10.1002/jcp.26838&rft_dat=%3Cproquest_cross%3E2068912925%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2118437532&rft_id=info:pmid/29995982&rfr_iscdi=true |