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Development of bioartificial myocardium by electrostimulation of 3D collagen scaffolds seeded with stem cells

机译:通过电刺激植入干细胞的3D胶原蛋白支架开发生物人工心肌

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摘要

Electrostimulation (ES) can be defined as a safe physical method to induce stem cell differentiation. The aim of this study is to evaluate the effectiveness of ES on bone marrow mesenchymal stem cells (BMSCs) seeded in collagen scaffolds in terms of proliferation and differentiation into cardiomyocytes. BMSCs were isolated from Wistar rats and seeded into 3D collagen type 1 templates measuring 25 × 25 × 6 mm. Bipolar in vitro ES was performed during 21 days. Electrical impedance and cell proliferation were measured. Expression of cardiac markers was assessed by immunocytochemistry. Viscoelasticity of collagen matrix was evaluated. Electrical impedance assessments showed a low resistance of 234±41 Ohms which indicates good electrical conductivity of collagen matrix. Cell proliferation at 570 nm as significantly increased in ES groups after seven day (ES 0.129±0.03 vs non-stimulated control matrix 0.06±0.01, P=0.002) and after 21 days, (ES 0.22±0.04 vs control 0.13±0.01, P=0.01). Immunocytoche mistry of BMSCs after 21 days ES showed positive staining of cardiac markers, troponin I, connexin 43, sarcomeric alpha-actinin, slow myosin, fast myosin and desmin. Staining for BMSCs marker CD29 after 21 days was negative. Electrostimulation of cell-seeded collagen matrix changed stem cell morphology and biochemical characteristics, increasing the expression of cardiac markers. Thus, MSC-derived differentiated cells by electrostimulation grafted in biological scaffolds might result in a convenient tissue engineering source for myocardial diseases.
机译:电刺激(ES)可以定义为诱导干细胞分化的安全物理方法。这项研究的目的是评估ES对胶原支架中骨髓间充质干细胞(BMSCs)增殖和分化为心肌细胞的有效性。从Wistar大鼠中分离出BMSC,并将其植入尺寸为25×25×6 mm的3D 1型胶原蛋白模板中。在21天内进行了双极体外ES。测量电阻抗和细胞增殖。通过免疫细胞化学评估心脏标志物的表达。评价胶原蛋白基质的粘弹性。电阻抗评估显示出234±41欧姆的低电阻,这表明胶原蛋白基质具有良好的导电性。 ES组在570 nm处的细胞增殖在7天后(ES 0.129±0.03与未刺激的对照基质0.06±0.01,P = 0.002)和在21天后(ES 0.22±0.04与对照0.13±0.01,P = 0.01)。 ES第21天后,BMSCs的免疫细胞模糊显示心脏标志物,肌钙蛋白I,连接蛋白43,肌节α-肌动蛋白,慢肌球蛋白,快肌球蛋白和结蛋白呈阳性染色。 21天后,BMSCs标记CD29的染色为阴性。细胞接种的胶原蛋白基质的电刺激改变了干细胞的形态和生化特性,增加了心脏标志物的表达。因此,通过电刺激移植到生物支架中的MSC衍生的分化细胞可能会为心肌疾病提供方便的组织工程来源。

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