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Joint meeting of British Societies for Matrix Biology and Developmental Biology 'The musculoskeletal system; from development to disease' Abstracts

机译:英国基质生物学和发育生物学学会联席会议“肌肉骨骼系统;从发展到疾病的文摘

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The aim of this study was to develop a method to generate multi-organ acellular matrices. Using a foetal sheep model have developed a method of systemic pulsatile perfusion via the umbilical artery which allows for simultaneous multi-organ decellularization. Twenty sheep foetuses were systemically perfused with Triton X-100 and sodium dodecyl sulphate. Following completion of the whole-body decellularization, multiple biopsy samples were taken from different parts of 21 organs to ascertain complete cell component removal in the preserved extracellular matrices. Both the natural and decellularized organs were subjected to several examinations. The samples were obtained from the skin, eye, ear, nose, throat, cardiovascular, respiratory, gastrointestinal, urinary, musculoskeletal, central nervous and peripheral nervous systems. The histological results depicted well-preserved extracellular matrix (ECM) integrity and intact vascular structures, without any evidence of residual cellular materials, in all decellularized bioscaffolds. Scanning electron microscope (SEM) and biochemical properties remained intact, similar to their age-matched native counterparts. Preservation of the collagen structure was evaluated by a hydroxyproline assay. Dense organs such as bone and muscle were also completely decellularized, with a preserved ECM structure. Thus, as shown in this study, several organs and different tissues were decellularized using a perfusion-based method, which has not been previously accomplished. Given the technical challenges that exist for the efficient generation of biological scaffolds, the current results may pave the way for obtaining a variety of decellularized scaffolds from a single donor. In this study, there have been unique responses to the single acellularization protocol in foetuses, which may reflect the homogeneity of tissues and organs in the developing foetal body.
机译:这项研究的目的是开发一种生成多器官脱细胞基质的方法。使用胎羊模型已经开发了一种通过脐动脉进行系统性脉动灌注的方法,该方法允许同时进行多器官脱细胞。用Triton X-100和十二烷基硫酸钠全身灌注20只绵羊胎儿。全身脱细胞完成后,从21个器官的不同部位采集了多个活检样品,以确定在保存的细胞外基质中细胞成分已完全去除。天然器官和脱细胞器官均接受了几次检查。样品是从皮肤,眼睛,耳朵,鼻子,喉咙,心血管,呼吸道,胃肠道,泌尿道,肌肉骨骼,中枢神经系统和周围神经系统获得的。组织学结果显示在所有脱细胞的生物支架中,保存完好的细胞外基质(ECM)完整性和完整的血管结构,没有任何残留细胞物质的证据。扫描电子显微镜(SEM)和生化特性保持不变,与它们的年龄匹配的天然类似物相似。通过羟脯氨酸测定法评估胶原结构的保存。密集的器官(如骨骼和肌肉)也被完全脱细胞,并保留了ECM结构。因此,如本研究中所示,使用基于灌注的方法对几个器官和不同组织进行了脱细胞处理,这是以前没有完成的。考虑到有效产生生物支架存在的技术挑战,当前的结果可能为从单个供体获得各种脱细胞支架铺平道路。在这项研究中,对胎儿中的单个脱细胞方案有独特的反应,这可能反映了发育中的胎儿体内组织和器官的均质性。

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