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用于在聚四氟乙烯和可生物降解聚酯上对聚多巴胺和VAPG肽进行图案化以实现体外平滑肌细胞图案化生长的系统。

System for Patterning Polydopamine and VAPG Peptide on Polytetrafluoroethylene and Biodegradable Polyesters for Patterned Growth of Smooth Muscle Cells In Vitro.

作者信息

Kopeć Kamil, Podgórski Rafał, Ciach Tomasz, Wojasiński Michał

机构信息

Warsaw University of Technology, Faculty of Chemical and Process Engineering, Department of Biotechnology and Bioprocess Engineering, Waryńskiego 1, 00-645 Warsaw, Poland.

Warsaw University of Technology, CEZAMAT, Poleczki 19, 02-822 Warsaw, Poland.

出版信息

ACS Omega. 2023 Jun 5;8(24):22055-22066. doi: 10.1021/acsomega.3c02114. eCollection 2023 Jun 20.

Abstract

Biomaterial's surface functionalization for selective adhesion and patterned cell growth remains essential in developing novel implantable medical devices for regenerative medicine applications. We built and applied a 3D-printed microfluidic device to fabricate polydopamine (PDA) patterns on the surface of polytetrafluoroethylene (PTFE), poly(l-lactic acid--D,l-lactic acid) (PLA), and poly(lactic acid--glycolic acid) (PLGA). Then, we covalently attached the Val-Ala-Pro-Gly (VAPG) peptide to the created PDA pattern to promote the adhesion of the smooth muscle cells (SMCs). We proved that the fabrication of PDA patterns allows for the selective adhesion of mouse fibroblast and human SMCs to PDA-patterned surfaces after only 30 min of in vitro cultivation. After 7 days of SMC culture, we observed the proliferation of cells only along the patterns on PTFE but over the entire surface of the PLA and PLGA, regardless of patterning. This means that the presented approach is beneficial for application to materials resistant to cell adhesion and proliferation. The additional attachment of the VAPG peptide to the PDA patterns did not bring measurable benefits due to the high increase in adhesion and patterned cell proliferation by PDA itself.

摘要

在开发用于再生医学应用的新型可植入医疗设备时,生物材料的表面功能化以实现选择性粘附和图案化细胞生长仍然至关重要。我们构建并应用了一种3D打印的微流控设备,在聚四氟乙烯(PTFE)、聚(L-乳酸-D,L-乳酸)(PLA)和聚(乳酸-乙醇酸)(PLGA)表面制造聚多巴胺(PDA)图案。然后,我们将Val-Ala-Pro-Gly(VAPG)肽共价连接到创建的PDA图案上,以促进平滑肌细胞(SMC)的粘附。我们证明,在体外培养仅30分钟后,PDA图案的制造就能使小鼠成纤维细胞和人SMC选择性粘附到PDA图案化的表面上。在SMC培养7天后,我们观察到细胞仅沿着PTFE上的图案增殖,但在PLA和PLGA的整个表面上增殖,无论是否有图案。这意味着所提出的方法有利于应用于抗细胞粘附和增殖的材料。由于PDA本身会使粘附和图案化细胞增殖大幅增加,因此将VAPG肽额外连接到PDA图案上并没有带来可测量的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/402b/10285958/be0bbb112121/ao3c02114_0002.jpg

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