Decellularization of heart valve matrices: search for the ideal balance.

Pamela Somers, Filip De Somer, Maria Cornelissen, Hubert Thierens, Guido Van Nooten
{"title":"Decellularization of heart valve matrices: search for the ideal balance.","authors":"Pamela Somers,&nbsp;Filip De Somer,&nbsp;Maria Cornelissen,&nbsp;Hubert Thierens,&nbsp;Guido Van Nooten","doi":"10.3109/10731199.2011.637925","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Currently used decellularization procedures have negative effects on extracellular matrix (ECM) integrity. The objective of this study is to evaluate four decellularization methods and their effect on the collagen ultrastructure, mechanical behavior and antigenicity of porcine aortic valves.</p><p><strong>Methods: </strong>Aortic valves were placed in a trypsin, osmotic, trypsin-osmotic or detergent-osmotic solution. Leaflets were processed for histology and mechanical testing. Matrices were implanted subdermally in rats to evaluate immune reaction and calcification.</p><p><strong>Results: </strong>Trypsin-osmotic methodology effected near-complete decellularization. Trypsin treatment resulted in cell removal only in the spongiosa layer. Osmotic and detergent-osmotic treatments did not remove any cells from the cusps. Mechanical strength was significantly inferior in the trypsin (p50,03) and trypsin-osmotic treated group (p50,04). Trypsin and trypsin-osmotic decellularized matrices evoked a strong CD31 inflammatory cell infiltration.</p><p><strong>Conclusion: </strong>Enzymatic-osmotic decellularization appears to be the only effective method to remove cellular components. However, the near cell free scaffolds still evokes a strong CD31 T-cell inflammatory reaction.</p>","PeriodicalId":8413,"journal":{"name":"Artificial cells, blood substitutes, and immobilization biotechnology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2012-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/10731199.2011.637925","citationCount":"34","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Artificial cells, blood substitutes, and immobilization biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10731199.2011.637925","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2011/12/22 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 34

Abstract

Objective: Currently used decellularization procedures have negative effects on extracellular matrix (ECM) integrity. The objective of this study is to evaluate four decellularization methods and their effect on the collagen ultrastructure, mechanical behavior and antigenicity of porcine aortic valves.

Methods: Aortic valves were placed in a trypsin, osmotic, trypsin-osmotic or detergent-osmotic solution. Leaflets were processed for histology and mechanical testing. Matrices were implanted subdermally in rats to evaluate immune reaction and calcification.

Results: Trypsin-osmotic methodology effected near-complete decellularization. Trypsin treatment resulted in cell removal only in the spongiosa layer. Osmotic and detergent-osmotic treatments did not remove any cells from the cusps. Mechanical strength was significantly inferior in the trypsin (p50,03) and trypsin-osmotic treated group (p50,04). Trypsin and trypsin-osmotic decellularized matrices evoked a strong CD31 inflammatory cell infiltration.

Conclusion: Enzymatic-osmotic decellularization appears to be the only effective method to remove cellular components. However, the near cell free scaffolds still evokes a strong CD31 T-cell inflammatory reaction.

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
心脏瓣膜基质的脱细胞:寻找理想的平衡。
目的:目前使用的脱细胞方法对细胞外基质(ECM)的完整性有负面影响。本研究旨在评价四种脱细胞方法对猪主动脉瓣胶原超微结构、力学行为和抗原性的影响。方法:将主动脉瓣置于胰蛋白酶、渗透、胰蛋白酶渗透或洗涤渗透溶液中。对小叶进行组织学和力学试验。将基质植入大鼠皮下,观察其免疫反应和钙化情况。结果:胰蛋白酶渗透法实现了近乎完全的脱细胞。胰蛋白酶处理只导致海绵层的细胞去除。渗透和洗涤剂渗透处理没有从尖端去除任何细胞。胰蛋白酶组(p50,03)和胰蛋白酶渗透处理组(p50,04)机械强度明显低于对照组(p50,04)。胰蛋白酶和胰蛋白酶-渗透脱细胞基质诱导强烈的CD31炎性细胞浸润。结论:酶渗透脱细胞是清除细胞成分的唯一有效方法。然而,近细胞游离支架仍然引起强烈的CD31 t细胞炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊最新文献
Covalent immobilization of trypsin on glutaraldehyde-activated silica for protein fragmentation. In vitro effect of novel β-lactam compounds on xanthine oxidase enzyme activity. Chitosan-based intragastric delivery of cefuroxime axetil: development and in-vitro evaluation of mucoadhesive approach. Purification and characterization of prophenoloxidase from Galleria mellonella L. Immobilization of anti-aflatoxin B1 antibody by UV polymerization of aniline and aflatoxin B1 detection via electrochemical impedance spectroscopy.
×
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