Improved in vitro endothelialization on nanostructured titania with tannin/glycosaminoglycan-based polyelectrolyte multilayers

被引:1
作者
Sabino, Roberta M. [1 ,2 ]
Kipper, Matt J. [1 ,3 ,4 ]
Martins, Alessandro F. [4 ,5 ,6 ]
Popat, Ketul C. [1 ,3 ,7 ]
机构
[1] Colorado State Univ, Sch Adv Mat Discovery, Ft Collins, CO 80523 USA
[2] MIT, Inst Med Engn & Sci, Cambridge, MA USA
[3] Colorado State Univ, Sch Biomed Engn, Ft Collins, CO 80523 USA
[4] Colorado State Univ, Dept Chem & Biol Engn, Ft Collins, CO USA
[5] Fed Univ Technol, Lab Mat Macromol & Composites, Curitiba, Brazil
[6] Univ Estadual Maringa, Chem Dept, Grp Polymers & Composite Mat, Maringa, Brazil
[7] Colorado State Univ, Dept Mech Engn, Ft Collins, CO 80523 USA
来源
IN VITRO MODELS | 2022年 / 1卷 / 03期
基金
美国国家卫生研究院;
关键词
Endothelialization; Titanium; polyelectrolyte multilayer; Tanfloc; Heparin; EXTRACELLULAR-MATRIX; HEPARIN; SURFACE; PERFORMANCE; MEMBRANES; ADHESION; FILMS;
D O I
10.1007/s44164-022-00024-x
中图分类号
Q813 [细胞工程];
学科分类号
摘要
PurposeBlood compatibility of cardiovascular implants is still a major concern. Rapid endothelialization of these implant surfaces has emerged as a promising strategy to enhance hemocompatibility and prevent complications such as thrombus formation and restenosis. The successful endothelialization of implant surfaces mostly depends on the migration of endothelial cells (ECs), the differentiation of stem cells, and the inhibition of smooth muscle cell (SMC) proliferation. Our previous study demonstrated that nanostructured titania surfaces modified with polyelectrolyte multilayers based on tanfloc (a cationic tannin derivative) and glycosaminoglycans (heparin and hyaluronic acid) have improved antithrombogenic properties.MethodsIn this work, we used in vitro cell culture of ECs and SMCs to investigate the outcomes of these surface modifications on endothelialization. The cells were seeded on the surfaces, and their viability, adhesion, and proliferation were evaluated after 1, 3, and 5 days. Indirect immunofluorescent staining was used to determine the cellular expression of ECs through the presence of specific marker proteins after 7 and 10 days, and EC migration on the NT surfaces was also investigated.ResultsThe surfaces modified with tanfloc and heparin showed enhanced EC adhesion, proliferation, and migration. However, SMC proliferation is not promoted by the surfaces. Therefore, these surfaces may promote endothelialization without stimulating SMC proliferation, which could improve the hemocompatibility without enhancing the risk of SMC proliferation leading to restenosis.ConclusionsThe surface modification here proposed is a promising candidate to be used in cardiovascular applications due to enhanced antithrombogenic and endothelialization properties.
引用
收藏
页码:249 / 259
页数:11
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