Conductive chitosan/polyaniline hydrogel with cell-imprinted topography as a potential substrate for neural priming of adipose derived stem cells. Issue 26 (28th April 2021)

• Record Type: Journal Article
• Authors: Eftekhari, Behnaz Sadat; Eskandari, Mahnaz; Janmey, Paul A.; Samadikuchaksaraei, Ali; Gholipourmalekabadi, Mazaher
• Is Part Of: RSC advances. Volume 11:Issue 26(2021)
• Page Start: 15795
• Page End: 15807
• Publication Date: 2021-04-28
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra00413a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A conductive chitosan/polyaniline hydrogel with cell-imprinted topography was used for neural priming of adipose derived stem cells. Abstract : Biophysical characteristics of engineered scaffolds such as topography and electroconductivity have shown potentially beneficial effects on stem cell morphology, proliferation, and differentiation toward neural cells. In this study, we fabricated a conductive hydrogel made from chitosan (CS) and polyaniline (PANI) with induced PC12 cell surface topography using a cell imprinting technique to provide both topographical properties and conductivity in a platform. The engineered hydrogel's potential for neural priming of rat adipose-derived stem cells (rADSCs) was determined in vitro . The biomechanical analysis revealed that the electrical conductivity, stiffness, and hydrophobicity of flat (F) and cell-imprinted (CI) substrates increased with increased PANI content in the CS/PANI scaffold. The conductive substrates exhibited a lower degradation rate compared to non-conductive substrates. According to data obtained from F-actin staining and AFM micrographs, both CI(CS) and CI(CS–PANI) substrates induced the morphology of rADSCs from their irregular shape (on flat substrates) into the elongated and bipolar shape of the neuronal-like PC12 cells. Immunostaining analysis revealed that both CI(CS) and CI (CS–PANI) significantly upregulated the expression of GFAP and MAP2, two neural precursor-specific genes, in rADSCs compared with flat substrates. Although the results reveal that both cell-imprinted topography and electrical conductivity affect the neural lineage differentiation, some data demonstrate that the topography effects of the cell-imprinted surface have a more critical role than electrical conductivity on neural priming of ADSCs. The current study provides new insight into the engineering of scaffolds for nerve tissue engineering.