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人心脏细胞外基质-壳聚糖-明胶复合支架及其内皮化

Human cardiac extracellular matrix-chitosan-gelatin composite scaffold and its endothelialization.

作者信息

Lv Jingjing, Liu Wei, Shi Guocheng, Zhu Fang, He Xiaomin, Zhu Zhongqun, Chen Huiwen

机构信息

Heart Center, Shanghai Children's Medical Center, Shanghai Jiaotong University, School of Medicine, Shanghai 200127, P.R. China.

Department of Pediatric Cardiothoracic Surgery, Xinhua Hospital Affiliated to Shanghai Jiaotong University, School of Medicine, Shanghai 200092, P.R. China.

出版信息

Exp Ther Med. 2020 Feb;19(2):1225-1234. doi: 10.3892/etm.2019.8349. Epub 2019 Dec 19.

Abstract

The present study developed a cardiac extracellular matrix-chitosan-gelatin (cECM-CG) composite scaffold that can be used as a tissue-engineered heart patch and investigated its endothelialization potential by incorporating CD34 endothelial progenitor cells (EPCs). The cECM-CG composite scaffold was prepared by blending cardiac extracellular matrix (cECM) with biodegradable chitosan-gelatin (CG). The mixture was lyophilized using vacuum freeze-drying. CD34 EPCs were isolated and seeded on the scaffolds, and then the endothelialization effect was subsequently investigated. Effects of the scaffolds on CD34 EPCs survival and proliferation were evaluated by immunofluorescence staining and MTT assay. Cell differentiation into endothelial cells and the influence of the scaffolds on cell differentiation were investigated by reverse transcription-quantitative PCR (RT-qPCR), immunofluorescence staining and tube formation assay. The present results indicated that most cells were removed after decellularization, but the main extracellular matrix components were retained. Scanning electron microscopy imaging illustrated three-dimensional and porous scaffolds. The present results suggested the cECM-CG composite scaffold had a higher water absorption ability compared with the CG scaffold. Additionally, compared with the CG scaffold, the cECM-CG composite scaffold significantly increased cell survival and proliferation, which suggested its non-toxicity and biocompatibility. Furthermore, RT-qPCR, immunofluorescence and tube formation assay results indicated that CD34 EPCs differentiated into endothelial cells, and the cECM-CG composite scaffold promoted this differentiation process. In conclusion, the present results indicated that the human cECM-CG composite scaffold generated in the present study was a highly porous, biodegradable three-dimensional scaffold which supported endothelialization of seeded CD34 EPCs. The present results suggested that this cECM-CG composite scaffold may be a promising heart patch for use in heart tissue engineering for congenital heart disease.

摘要

本研究开发了一种可作为组织工程心脏补片的心脏细胞外基质-壳聚糖-明胶(cECM-CG)复合支架,并通过掺入CD34内皮祖细胞(EPCs)研究了其内皮化潜力。cECM-CG复合支架是通过将心脏细胞外基质(cECM)与可生物降解的壳聚糖-明胶(CG)混合制备而成。该混合物采用真空冷冻干燥法进行冻干。分离出CD34 EPCs并接种到支架上,随后研究内皮化效果。通过免疫荧光染色和MTT法评估支架对CD34 EPCs存活和增殖的影响。通过逆转录定量PCR(RT-qPCR)、免疫荧光染色和管腔形成试验研究细胞向内皮细胞分化以及支架对细胞分化的影响。目前的结果表明,去细胞处理后大部分细胞被去除,但主要的细胞外基质成分得以保留。扫描电子显微镜成像显示为三维多孔支架。目前的结果表明,与CG支架相比,cECM-CG复合支架具有更高的吸水能力。此外,与CG支架相比,cECM-CG复合支架显著提高了细胞存活和增殖能力,这表明其具有无毒性和生物相容性。此外,RT-qPCR、免疫荧光和管腔形成试验结果表明,CD34 EPCs分化为内皮细胞,且cECM-CG复合支架促进了这一分化过程。总之,目前的结果表明,本研究中制备的人cECM-CG复合支架是一种高度多孔、可生物降解的三维支架,可支持接种的CD34 EPCs的内皮化。目前的结果表明,这种cECM-CG复合支架可能是用于先天性心脏病心脏组织工程的一种有前景的心脏补片。

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