In vitro characterization of a nanostructured fibrin agarose bio‐artificial nerve substitute. (14th July 2015)

• Record Type: Journal Article
• Authors: Carriel, Víctor; Scionti, Giuseppe; Campos, Fernando; Roda, Olga; Castro, Begoña; Cornelissen, Maria; Garzón, Ingrid; Alaminos, Miguel
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 11:Number 5(2017)
• Page Start: 1412
• Page End: 1426
• Publication Date: 2015-07-14
• Subjects: neural tissue engineering -- biomimetic nerve substitute -- fibrin–agarose hydrogels -- nanostructured biomaterials -- adipose‐derived mesenchymal stem cells -- extracellular matrix -- cell–biomaterial interactions; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.2039
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: Neural tissue engineering is focused on the design of novel biocompatible substitutes to repair peripheral nerve injuries. In this paper we describe a nanostructured fibrin–agarose bioartificial nerve substitute (NFABNS), based on nanostructured fibrin–agarose hydrogels (FAHs) with human adipose‐derived mesenchymal stem cells (HADMSCs). These NFABNSs were mechanically characterized and HADMSCs behaviour was evaluated using histological and ultrastructural techniques. Mechanical characterization showed that the NFABNSs were resistant, flexible and elastic, with a high deformation capability. Histological analyses carried out in vitro during 16 days revealed that the number of HADMSCs decreased over time, with a significant increase after 16 days. HADMSCs formed cell clusters and degraded the surrounding scaffold during this time; additionally, HADMSCs showed active cell proliferation and cytoskeletal remodelling, with a progressive synthesis of extracellular matrix molecules. Finally, this study demonstrated that it is possible to generate biologically active and mechanically stable tissue‐like substitutes with specific dimensions, based on the use of HADMSCs, FAHs and a nanostructure technique. However, in vivo analyses are needed to demonstrate their potential usefulness in peripheral nerve repair. Copyright © 2015 John Wiley & Sons, Ltd.