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用于未来再生医学的、采用干细胞片技术制备的一种潜在生物材料的制造与评估。

The Fabrication and Evaluation of a Potential Biomaterial Produced with Stem Cell Sheet Technology for Future Regenerative Medicine.

作者信息

Zhou Shukui, Wang Ying, Zhang Kaile, Cao Nailong, Yang Ranxing, Huang Jianwen, Zhao Weixin, Rahman Mahbubur, Liao Hong, Fu Qiang

机构信息

Department of Urology, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

Department of Urology, Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Stem Cells Int. 2020 Feb 10;2020:9567362. doi: 10.1155/2020/9567362. eCollection 2020.

Abstract

To date, the decellularized scaffold has been widely explored as a source of biological scaffolds for regenerative medicine. However, the acellular matrix derived from natural tissues and organs has a lot of defects, including the limited amount of autogenous tissue and surgical complication such as risk of blood loss, wound infection, pain, shock, and functional damage in the donor part of the body. In this study, we prepared acellular matrix using adipose-derived stem cell (ADSC) sheets and evaluate the cellular compatibility and immunoreactivity. The ADSC sheets were fabricated and subsequently decellularized using repeated freeze-thaw, Triton X-100 and SDS decellularization. Oral mucosal epithelial cells were seeded onto the decellularized ADSC sheets to evaluate the cell replantation ability, and silk fibroin was used as the control. Then, acellular matrix was transplanted onto subcutaneous tissue for 1 week or 3 weeks; H&E staining and immunohistochemical analysis of CD68 expression and quantitative real-time PCR (qPCR) were performed to evaluate the immunogenicity and biocompatibility. The ADSC sheet-derived ECM scaffolds preserved the three-dimensional architecture of ECM and retained the cytokines by Triton X-100 decellularization protocols. Compared with silk fibroin in vitro, the oral mucosal epithelial cells survived better on the decellularized ADSC sheets with an intact and consecutive epidermal cellular layer. Compared with porcine small intestinal submucosa (SIS) in vivo, the homogeneous decellularized ADSC sheets had less monocyte-macrophage infiltrating in vivo implantation. During 3 weeks after transplantation, the mRNA expression of cytokines, such as IL-4/IL-10, was obviously higher in decellularized ADSC sheets than that of porcine SIS. A Triton X-100 method can achieve effective cell removal, retain major ECM components, and preserve the ultrastructure of ADSC sheets. The decellularized ADSC sheets possess good recellularization capacity and excellent biocompatibility. This study demonstrated the potential suitability of utilizing acellular matrix from ADSC sheets for soft tissue regeneration and repair.

摘要

迄今为止,脱细胞支架作为再生医学中生物支架的来源已得到广泛研究。然而,源自天然组织和器官的无细胞基质存在许多缺陷,包括自体组织数量有限以及手术并发症,如失血风险、伤口感染、疼痛、休克以及身体供体部位的功能损害。在本研究中,我们使用脂肪来源干细胞(ADSC)片制备无细胞基质,并评估其细胞相容性和免疫反应性。制备ADSC片,随后通过反复冻融、Triton X - 100和SDS脱细胞处理使其脱细胞。将口腔黏膜上皮细胞接种到脱细胞的ADSC片上以评估细胞再植能力,并以丝素蛋白作为对照。然后,将无细胞基质移植到皮下组织1周或3周;进行苏木精 - 伊红(H&E)染色以及CD68表达的免疫组织化学分析和定量实时聚合酶链反应(qPCR),以评估免疫原性和生物相容性。ADSC片来源的细胞外基质(ECM)支架通过Triton X - 100脱细胞方案保留了ECM的三维结构并保留了细胞因子。与体外的丝素蛋白相比,口腔黏膜上皮细胞在具有完整且连续表皮细胞层的脱细胞ADSC片上存活得更好。与体内的猪小肠黏膜下层(SIS)相比,均匀的脱细胞ADSC片在体内植入时单核细胞 - 巨噬细胞浸润较少。在移植后3周内,脱细胞ADSC片中细胞因子如白细胞介素 - 4/白细胞介素 - 10的mRNA表达明显高于猪SIS。Triton X - 100方法可以实现有效的细胞去除,保留主要的ECM成分,并保留ADSC片的超微结构。脱细胞的ADSC片具有良好的再细胞化能力和优异的生物相容性。本研究证明了利用ADSC片的无细胞基质进行软组织再生和修复的潜在适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3277/7035578/e7edb60e25f8/SCI2020-9567362.001.jpg

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