Conductive chitosan/polyaniline hydrogel with cell-imprinted topography as a potential substrate for neural priming of adipose derived stem cells

被引:28
作者
Eftekhari, Behnaz Sadat [1 ,2 ]
Eskandari, Mahnaz [1 ]
Janmey, Paul A. [2 ]
Samadikuchaksaraei, Ali [3 ]
Gholipourmalekabadi, Mazaher [3 ,4 ,5 ]
机构
[1] Amirkabir Univ Technol, Dept Biomed Engn, 424 Hafez Ave, Tehran 158754413, Iran
[2] Univ Penn, Inst Med & Engn, Dept Physiol, Vagelos Res Labs 1010, 3340 Smith Walk, Philadelphia, PA 19104 USA
[3] Iran Univ Med Sci, Cellular & Mol Res Ctr, Tehran, Iran
[4] Iran Univ Med Sci, Fac Allied Med, Dept Med Biotechnol, Tehran, Iran
[5] Iran Univ Med Sci, Fac Adv Technol Med, Dept Tissue Engn & Regenerat Med, Tehran, Iran
基金
美国国家科学基金会;
关键词
SPINAL-CORD-INJURY; DRUG-DELIVERY; SURFACE-TOPOGRAPHY; CHITOSAN ACETATE; IN-VITRO; TISSUE; DIFFERENTIATION; NANOPARTICLES; EXPRESSION; BEHAVIOR;
D O I
10.1039/d1ra00413a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:15795 / 15807
页数:13
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