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组合去细胞化作为一种制备具有保留生物活性的猪肝细胞外基质支架的更好方法:一项比较评估

Combinatorial Decellularization as a Better Approach to Porcine Liver Extracellular Matrix Scaffold Fabrication With Preserved Bioactivity: A Comparative Evaluation.

作者信息

Puthiya Veettil Jesna, Sasikumar Lolitha Devika, Payanam Ramachandra Umashankar

机构信息

Division of In-Vivo Models and Testing, Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, India.

出版信息

Xenotransplantation. 2025 Mar-Apr;32(2):e70031. doi: 10.1111/xen.70031.

DOI:10.1111/xen.70031
PMID:40106378
Abstract

Soft tissue repair patches of decellularized extracellular matrices (ECM) with inherently preserved structural components and biomacromolecules are desirable in regenerative applications. This study characterizes three detergent-based decellularization methods to fabricate acellular porcine liver matrices to remove antigenic determinants without compromising the structural integrity, glycosaminoglycans (GAG) content, and bound growth factors within the resulting ECM. Three detergents chosen for decellularization were sodium dodecyl sulfate (SDS), SDS with sodium deoxycholate (SDS+SDC-combinatorial method), and triton X-100 followed by SDS. Combinatorial detergent decellularization effectively removed cellular components and retained intact collagenous structure with minimal residual DNA and protein. It also preserved significantly higher amounts of GAG, HGF, and bFGF. TX100 decellularization was highly destructive with the least preservation of GAG and GFs. The SDS method showed an intermediate level of preservation of biomolecules. The correlation obtained between GAG and GFs revealed quantification of GAG to be an indirect way of estimating the bound GFs preserved within the ECM. In vitro experiments revealed the non-cytotoxic nature of the scaffolds. The study revealed that, among the three methods of decellularization, the ECM scaffold fabricated by combinatorial detergent decellularization is extremely promising to be used as a soft tissue repair patch with inherent bioactive molecules for scaffold-based regenerative therapies.

摘要

具有固有保留结构成分和生物大分子的去细胞化细胞外基质(ECM)软组织修复贴片在再生应用中是理想的。本研究对三种基于去污剂的去细胞化方法进行了表征,以制备无细胞猪肝脏基质,在不损害所得ECM的结构完整性、糖胺聚糖(GAG)含量和结合生长因子的情况下去除抗原决定簇。选择用于去细胞化的三种去污剂分别是十二烷基硫酸钠(SDS)、SDS与脱氧胆酸钠(SDS + SDC组合法)以及先使用曲拉通X - 100再使用SDS。组合去污剂去细胞化有效地去除了细胞成分,并保留了完整的胶原结构,残留的DNA和蛋白质最少。它还保留了显著更多的GAG、HGF和bFGF。TX100去细胞化具有高度破坏性,对GAG和生长因子的保留最少。SDS方法显示出生物分子保留处于中等水平。GAG与生长因子之间的相关性表明,对GAG进行定量是估计ECM中保留的结合生长因子的一种间接方法。体外实验揭示了支架的无细胞毒性性质。该研究表明,在三种去细胞化方法中,通过组合去污剂去细胞化制备的ECM支架极有希望用作具有固有生物活性分子的软组织修复贴片,用于基于支架的再生疗法。

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