可变形活体结构的4D生物打印,具有持续的局部生长因子呈现,用于高级组织工程应用。

IF 5.4 2区 医学 Q1 BIOPHYSICS Colloids and Surfaces B: Biointerfaces Pub Date : 2024-12-27 DOI:10.1016/j.colsurfb.2024.114484
Guodong Wu , Lin Wang , Yuhang Cao , Manli Wang , Chun Yang , Jian Zhang
{"title":"可变形活体结构的4D生物打印,具有持续的局部生长因子呈现,用于高级组织工程应用。","authors":"Guodong Wu ,&nbsp;Lin Wang ,&nbsp;Yuhang Cao ,&nbsp;Manli Wang ,&nbsp;Chun Yang ,&nbsp;Jian Zhang","doi":"10.1016/j.colsurfb.2024.114484","DOIUrl":null,"url":null,"abstract":"<div><div>Traditional tissue engineering strategies focus on geometrically static tissue scaffolds, lacking the dynamic capability found in native tissues. The emerging field of 4D bioprinting offers a promising method to address this challenge. However, the requirement for consistent exogenous supplementation of growth factors (GFs) during tissue maturation poses a significant obstacle for in vivo application of 4D bioprinted constructs. We herein developed composite bioinks composed of photocrosslinkable, jammed alginate methacrylate (AlgMA) and gelatin methacrylate (GelMA), incorporating GelMA microspheres loaded with GFs to provide sustained local GF presentation over 50 days for 4D tissue bioprinting. The composite bioink exhibited excellent printability, enabling 3D printing with good accuracy (∼120 %) and fidelity (105 % − 114 %). By incorporating a photoabsorbent to enhance light attenuation, a gradient network along the light propagation pathway was generated, facilitating programmable and controllable 4D shape transformation. This process allowed the fabrication of complex living constructs with defined architectures through morphing. A proof-of-concept study on cartilage regeneration demonstrated the effectiveness of sustained GF presentation in driving tissue development, showing significant glycosaminoglycan production (GAG/DNA 10.3), and substantial upregulation of type II collagen (125.8-fold) and aggrecan (16.4-fold) mRNA expression, thereby eliminating the need for exogenous GF supplementation. This study underscores the transformative potential of integrating dynamic tissue scaffolding with sustained GF delivery, thereby addressing key limitations of traditional tissue engineering approaches and offering new avenues for tissue repair applications.</div></div>","PeriodicalId":279,"journal":{"name":"Colloids and Surfaces B: Biointerfaces","volume":"248 ","pages":"Article 114484"},"PeriodicalIF":5.4000,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"4D bioprinting of transformable living constructs with sustained local growth factor presentation for advanced tissue engineering applications\",\"authors\":\"Guodong Wu ,&nbsp;Lin Wang ,&nbsp;Yuhang Cao ,&nbsp;Manli Wang ,&nbsp;Chun Yang ,&nbsp;Jian Zhang\",\"doi\":\"10.1016/j.colsurfb.2024.114484\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Traditional tissue engineering strategies focus on geometrically static tissue scaffolds, lacking the dynamic capability found in native tissues. The emerging field of 4D bioprinting offers a promising method to address this challenge. However, the requirement for consistent exogenous supplementation of growth factors (GFs) during tissue maturation poses a significant obstacle for in vivo application of 4D bioprinted constructs. We herein developed composite bioinks composed of photocrosslinkable, jammed alginate methacrylate (AlgMA) and gelatin methacrylate (GelMA), incorporating GelMA microspheres loaded with GFs to provide sustained local GF presentation over 50 days for 4D tissue bioprinting. The composite bioink exhibited excellent printability, enabling 3D printing with good accuracy (∼120 %) and fidelity (105 % − 114 %). By incorporating a photoabsorbent to enhance light attenuation, a gradient network along the light propagation pathway was generated, facilitating programmable and controllable 4D shape transformation. This process allowed the fabrication of complex living constructs with defined architectures through morphing. A proof-of-concept study on cartilage regeneration demonstrated the effectiveness of sustained GF presentation in driving tissue development, showing significant glycosaminoglycan production (GAG/DNA 10.3), and substantial upregulation of type II collagen (125.8-fold) and aggrecan (16.4-fold) mRNA expression, thereby eliminating the need for exogenous GF supplementation. This study underscores the transformative potential of integrating dynamic tissue scaffolding with sustained GF delivery, thereby addressing key limitations of traditional tissue engineering approaches and offering new avenues for tissue repair applications.</div></div>\",\"PeriodicalId\":279,\"journal\":{\"name\":\"Colloids and Surfaces B: Biointerfaces\",\"volume\":\"248 \",\"pages\":\"Article 114484\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2024-12-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Colloids and Surfaces B: Biointerfaces\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0927776524007434\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloids and Surfaces B: Biointerfaces","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927776524007434","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

摘要

传统的组织工程策略侧重于几何静态组织支架,缺乏天然组织的动态能力。新兴的4D生物打印领域为解决这一挑战提供了一个有前途的方法。然而,在组织成熟过程中需要持续的外源补充生长因子(GFs),这对4D生物打印构建体的体内应用构成了重大障碍。我们在此开发了复合生物墨水,由光交联的,堵塞的甲基丙烯酸海藻酸盐(AlgMA)和甲基丙烯酸明胶(GelMA)组成,结合GelMA微球装载GF,为4D组织生物打印提供持续50天的局部GF呈现。复合生物墨水表现出优异的可打印性,使3D打印具有良好的精度(~ 120 %)和保真度(105 % - 114 %)。通过加入光吸收剂来增强光衰减,沿着光传播路径产生梯度网络,促进可编程和可控的4D形状转换。这个过程允许通过变形制造具有定义架构的复杂活结构。一项关于软骨再生的概念验证研究表明,持续的GF呈现在推动组织发育方面的有效性,显示出显著的糖胺聚糖生成(GAG/DNA 10.3),以及II型胶原蛋白(125.8倍)和聚集蛋白(16.4倍)mRNA表达的大幅上调,从而消除了外源性GF补充的需要。这项研究强调了将动态组织支架与持续的GF输送相结合的变革潜力,从而解决了传统组织工程方法的关键局限性,并为组织修复应用提供了新的途径。
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
4D bioprinting of transformable living constructs with sustained local growth factor presentation for advanced tissue engineering applications
Traditional tissue engineering strategies focus on geometrically static tissue scaffolds, lacking the dynamic capability found in native tissues. The emerging field of 4D bioprinting offers a promising method to address this challenge. However, the requirement for consistent exogenous supplementation of growth factors (GFs) during tissue maturation poses a significant obstacle for in vivo application of 4D bioprinted constructs. We herein developed composite bioinks composed of photocrosslinkable, jammed alginate methacrylate (AlgMA) and gelatin methacrylate (GelMA), incorporating GelMA microspheres loaded with GFs to provide sustained local GF presentation over 50 days for 4D tissue bioprinting. The composite bioink exhibited excellent printability, enabling 3D printing with good accuracy (∼120 %) and fidelity (105 % − 114 %). By incorporating a photoabsorbent to enhance light attenuation, a gradient network along the light propagation pathway was generated, facilitating programmable and controllable 4D shape transformation. This process allowed the fabrication of complex living constructs with defined architectures through morphing. A proof-of-concept study on cartilage regeneration demonstrated the effectiveness of sustained GF presentation in driving tissue development, showing significant glycosaminoglycan production (GAG/DNA 10.3), and substantial upregulation of type II collagen (125.8-fold) and aggrecan (16.4-fold) mRNA expression, thereby eliminating the need for exogenous GF supplementation. This study underscores the transformative potential of integrating dynamic tissue scaffolding with sustained GF delivery, thereby addressing key limitations of traditional tissue engineering approaches and offering new avenues for tissue repair applications.
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
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
期刊最新文献
Highly sensitive quantification of carbon black in lung burden through simplified proteinase K-mediated digestion Editorial Board Colon-targeted dual-coating MOF nanoparticles for the delivery of curcumin with anti-inflammatory properties in the treatment of ulcerative colitis Platelet membrane-cloaked biomimetic nanoparticles for targeted acute lung injury therapy A CRISPR/Cas12a-based colorimetric AuNPs biosensor for naked-eye detection of pathogenic bacteria in clinical samples
×
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