转录后修饰调节异型球体上的祖细胞分化

IF 3.5 3区 医学 Q3 CELL & TISSUE ENGINEERING Tissue Engineering Part A Pub Date : 2024-07-03 DOI:10.1089/ten.TEA.2023.0279
Nazmiye Celik, Srinivas V Koduru, Dino J Ravnic, Ibrahim T Ozbolat, Daniel J Hayes
{"title":"转录后修饰调节异型球体上的祖细胞分化","authors":"Nazmiye Celik, Srinivas V Koduru, Dino J Ravnic, Ibrahim T Ozbolat, Daniel J Hayes","doi":"10.1089/ten.TEA.2023.0279","DOIUrl":null,"url":null,"abstract":"<p><p>Cell aggregates are widely used to study heterotypic cellular interactions during the development of vascularization <i>in vitro</i>. In this study, we examined heterotypic cellular spheroids made of adipose-derived stem cells and CD34<sup>+</sup>/CD31<sup>-</sup> endothelial progenitor cells induced by the transfection of miR-148b mimic for <i>de novo</i> induction of osteogenic differentiation and miR-210 mimic for <i>de novo</i> induction of endotheliogenesis, respectively. The effect of the microRNA (miRs) mimic treatment group and induction time on codifferentiation was assessed in spheroids formed of transfected cells over the course of a 4-week culture. Based on gene and protein markers of osteogenic and endotheliogenic differentiation, as well as mineralization assays, our results showed that miRs directed cell differentiation and that progenitor maturity influenced the development of heterotypic cellular regions in aggregates. Overall, the success of coculture to create a prevascularized bone model is dependent on a number of factors, particularly the induction time of differentiation before combining the multiple cell types in aggregates. The approach that has been proposed could be valuable in creating vascularized bone tissue by employing spheroids as the building blocks of more complex issues through the use of cutting-edge methods such as 3D bioprinting.</p>","PeriodicalId":56375,"journal":{"name":"Tissue Engineering Part A","volume":null,"pages":null},"PeriodicalIF":3.5000,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Posttranscriptional Modification to Modulate Progenitor Differentiation on Heterotypic Spheroids.\",\"authors\":\"Nazmiye Celik, Srinivas V Koduru, Dino J Ravnic, Ibrahim T Ozbolat, Daniel J Hayes\",\"doi\":\"10.1089/ten.TEA.2023.0279\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cell aggregates are widely used to study heterotypic cellular interactions during the development of vascularization <i>in vitro</i>. In this study, we examined heterotypic cellular spheroids made of adipose-derived stem cells and CD34<sup>+</sup>/CD31<sup>-</sup> endothelial progenitor cells induced by the transfection of miR-148b mimic for <i>de novo</i> induction of osteogenic differentiation and miR-210 mimic for <i>de novo</i> induction of endotheliogenesis, respectively. The effect of the microRNA (miRs) mimic treatment group and induction time on codifferentiation was assessed in spheroids formed of transfected cells over the course of a 4-week culture. Based on gene and protein markers of osteogenic and endotheliogenic differentiation, as well as mineralization assays, our results showed that miRs directed cell differentiation and that progenitor maturity influenced the development of heterotypic cellular regions in aggregates. Overall, the success of coculture to create a prevascularized bone model is dependent on a number of factors, particularly the induction time of differentiation before combining the multiple cell types in aggregates. The approach that has been proposed could be valuable in creating vascularized bone tissue by employing spheroids as the building blocks of more complex issues through the use of cutting-edge methods such as 3D bioprinting.</p>\",\"PeriodicalId\":56375,\"journal\":{\"name\":\"Tissue Engineering Part A\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tissue Engineering Part A\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1089/ten.TEA.2023.0279\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL & TISSUE ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tissue Engineering Part A","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1089/ten.TEA.2023.0279","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
引用次数: 0

摘要

细胞聚集体被广泛用于研究体外血管发育过程中的异型细胞相互作用。在这项研究中,我们研究了由脂肪来源干细胞(ADSCs)和CD34+/CD31-内皮祖细胞组成的异型细胞球,它们分别由转染miR-148b模拟物(用于从头诱导成骨分化)和miR-210模拟物(用于从头诱导内皮细胞生成)诱导而成。对转染细胞制成的球状体进行了为期4周的培养评估,以确定微RNA(miRs)模拟处理组和诱导时间对共分化的影响。我们的结果表明,miRs 引导细胞分化,聚集体中异型细胞区域的发展部分取决于祖细胞的成熟度,成骨和内皮细胞分化的基因和蛋白标记以及矿化试验证实了这一点。总之,共培养创建预血管化骨模型的成功与否取决于多种因素,特别是在将多种细胞类型组合成聚集体之前的诱导分化时间。所介绍的方法可用于利用三维生物打印等先进技术,将球形细胞作为更复杂问题的构件来制造血管化骨组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Posttranscriptional Modification to Modulate Progenitor Differentiation on Heterotypic Spheroids.

Cell aggregates are widely used to study heterotypic cellular interactions during the development of vascularization in vitro. In this study, we examined heterotypic cellular spheroids made of adipose-derived stem cells and CD34+/CD31- endothelial progenitor cells induced by the transfection of miR-148b mimic for de novo induction of osteogenic differentiation and miR-210 mimic for de novo induction of endotheliogenesis, respectively. The effect of the microRNA (miRs) mimic treatment group and induction time on codifferentiation was assessed in spheroids formed of transfected cells over the course of a 4-week culture. Based on gene and protein markers of osteogenic and endotheliogenic differentiation, as well as mineralization assays, our results showed that miRs directed cell differentiation and that progenitor maturity influenced the development of heterotypic cellular regions in aggregates. Overall, the success of coculture to create a prevascularized bone model is dependent on a number of factors, particularly the induction time of differentiation before combining the multiple cell types in aggregates. The approach that has been proposed could be valuable in creating vascularized bone tissue by employing spheroids as the building blocks of more complex issues through the use of cutting-edge methods such as 3D bioprinting.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Tissue Engineering Part A
Tissue Engineering Part A Chemical Engineering-Bioengineering
CiteScore
9.20
自引率
2.40%
发文量
163
审稿时长
3 months
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues.
期刊最新文献
Editorial for Special Issue on Artificial Intelligence in Tissue Engineering and Biology. The role of matrix stiffness and viscosity on lipid phenotype and fat lineage potential. Vascularization of Human Acellular Dermal Matrices: A Comparative Study in a Nonhuman Primate Model. Mapping Biomaterial Complexity by Machine Learning. Bi-layered Adipose Mesenchymal Cell Sheets Improve Bladder Compliance in Spinal Cord-Injured Rats.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1