In vitro assessment of electrospun polyamide‐6 scaffolds for esophageal tissue engineering. Issue 2 (30th March 2018)

• Record Type: Journal Article
• Authors: Zhuravleva, Margarita; Gilazieva, Zarema; Grigoriev, Timofei E.; Shepelev, Alexey D.; Kh. Tenchurin, Timur; Kamyshinsky, Roman; Krasheninnikov, Sergey V.; Orlov, Sergei; Caralogli, Gina; Archipova, Svetlana; Holterman, Mark J.; Mavlikeev, Mikhail; Deev, Roman V.; Chvalun, Sergei N.; Macchiarini, Paolo
• Is Part Of: Journal of biomedical materials research. Volume 107:Issue 2(2019)
• Page Start: 253
• Page End: 268
• Publication Date: 2018-03-30
• Subjects: polyamide‐6 -- synthetic scaffolds -- electrospinning -- biocompatibility -- human mesenchymal stromal cells; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbm.b.34116
• Languages: English
• ISSNs: 1552-4973

Abstract

Abstract: Artificial tissue‐engineered grafts offer a potential alternative to autologous tissue grafts for patients, which can be traumatic. After decellularizing Papio hamadryas esophagus and studying the morphology and physical properties of the extracellular matrix (ECM), we generated electrospun polyamide‐6 based scaffolds to mimic it. The scaffolds supported a greater mechanical load than the native ECM and demonstrated similar 3D microstructure, with randomly aligned fibers, 90% porosity, 29 μm maximal pore size, and average fiber diameter of 2.87 ± 0.95 µm. Biocompatibility studies showed that human adipose‐ and bone marrow‐derived mesenchymal stromal cells (AD‐MSC and BMD‐MSC) adhered to the scaffold surface and showed some proliferation: scaffold cell coverage was 25% after 72 h of incubation when seeded with 1000 cells/mm 2 ; cells elongated processes along the polyamide‐6, although they flattened 1.67–4 times less than on cell culture plastic. Human umbilical vein endothelial cells, however, showed poor adherence and proliferation. We thus provide in vitro evidence that polyamide‐6 scaffolds approximating the esophageal biomechanics and 3D topography of nonhuman primates may provide a biocompatible substrate for both AD‐MSC and BMD‐MSCs, supporting their adhesion and survival to some degree. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 107B: 253–268, 2019.