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通过亲 CO 去污剂和超临界 CO 获得的去细胞组织。

Decellularised tissues obtained by a CO-philic detergent and supercritical CO.

机构信息

EPFL/STI/IBI/LBO, Station 9, 1015 Lausanne, Switzerland.

出版信息

Eur Cell Mater. 2018 Sep 4;36:81-95. doi: 10.22203/eCM.v036a07.

Abstract

Tissue decellularisation has gained much attention in regenerative medicine as an alternative to synthetic materials. In decellularised tissues, biological cues can be maintained and provide cellular environments still unmet by synthetic materials. Supercritical CO (scCO ) has recently emerged as a promising alternative decellularisation technique to aggressive detergents; in addition, scCO provides innate sterilisation. However, to date, decellularisation with scCO is limited to only a few tissue types with low cellular density. In the current study, a scCO technique to decellularise high density tissues, including articular cartilage, tendon and skin, was developed. Results showed that most of the cellular material was removed, while the sample structure and biocompatibility was preserved. The DNA content was reduced in cartilage, tendon and skin as compared to the native tissue. The treatment did not affect the initial tendon elastic modulus [reduced from 126.35 ± 9.79 MPa to 113.48 ± 8.48 MPa (p 〉 0.05)], while it reduced the cartilage one [from 12.06 ± 2.14 MPa to 1.17 ± 0.34 MPa (p 〈 0.0001)]. Interestingly, cell adhesion molecules such as fibronectin and laminin were still present in the tissues after decellularisation. Bovine chondrocytes were metabolically active and adhered to the surface of all decellularised tissues after 1 week of cell culture. The developed method has the potential to become a cost-effective, one-step procedure for the decellularisation of dense tissues.

摘要

组织脱细胞化在再生医学中受到广泛关注,作为合成材料的替代品。在脱细胞组织中,可以保留生物线索,并提供仍然无法满足合成材料的细胞环境。超临界 CO(scCO)最近作为一种有前途的替代去污剂的脱细胞化技术出现;此外,scCO 提供内在的杀菌作用。然而,迄今为止,scCO 脱细胞化仅限于少数细胞密度低的组织类型。在当前的研究中,开发了一种用于脱细胞化高密度组织(包括关节软骨、肌腱和皮肤)的 scCO 技术。结果表明,大部分细胞物质被去除,同时保留了样品结构和生物相容性。与天然组织相比,软骨、肌腱和皮肤中的 DNA 含量减少。该处理不会影响初始肌腱弹性模量[从 126.35±9.79 MPa 降低至 113.48±8.48 MPa(p 〉0.05)],但降低了软骨的弹性模量[从 12.06±2.14 MPa 降低至 1.17±0.34 MPa(p 〈0.0001)]。有趣的是,细胞黏附分子如纤连蛋白和层粘连蛋白在脱细胞化后仍存在于组织中。牛软骨细胞在细胞培养 1 周后在所有脱细胞组织表面均具有代谢活性并黏附。该方法具有成为致密组织脱细胞化的经济高效、一步法的潜力。

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