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培养时长对成骨细胞来源的脱细胞细胞外基质熔体静电纺丝支架骨形成能力的影响

Effect of Culture Length on the Bone-Forming Capacity of Osteoblast-Derived Decellularized Extracellular Matrix Melt Electrowritten Scaffolds.

作者信息

Blaudez Fanny, Ivanovski Saso, Fernandez Tulio, Vaquette Cedryck

机构信息

School of Dentistry and Oral Health, Griffith University, Parklands Dr., Southport QLD 4222, Australia.

The University of Queensland, School of Dentistry, 288 Herston Rd., Herston QLD 4006, Australia.

出版信息

Biomacromolecules. 2023 Aug 14;24(8):3450-3462. doi: 10.1021/acs.biomac.2c01504. Epub 2023 Jul 17.

Abstract

Recent advancements in decellularization have seen the development of extracellular matrix (ECM)-decorated scaffolds for bone regeneration; however, little is understood of the impact of culture prior to decellularization on the performances of these constructs. Therefore, this study investigated the effect of culture on ECM-decorated melt electrowritten polycaprolactone scaffold bioactivity. The scaffolds were seeded with osteoblasts and cultured for 1, 2, or 4 weeks to facilitate bone-specific ECM deposition and subsequently decellularized to form an acellular ECM-decorated scaffold. The utilization of mild chemicals and DNase was highly efficient in removing DNA while preserving ECM structure and composition. ECM decoration of the melt electrowritten fibers was observed within the first week of culture, with increased ECM at 2 and 4 week culture periods. Infiltration of re-seeded cells as well as overall bone regeneration in a rodent calvarial model was impeded by a longer culture period. Thus, it was demonstrated that the length of culture has a key influence on the osteogenic properties of decellularized ECM-decorated scaffolds, with long-term culture (2+ weeks) causing pore obstruction and creating a physical barrier which interfered with bone formation. These findings have important implications for the development of effective ECM-decorated scaffolds for bone regeneration.

摘要

脱细胞技术的最新进展促成了用于骨再生的细胞外基质(ECM)修饰支架的发展;然而,对于脱细胞前的培养对这些构建体性能的影响却知之甚少。因此,本研究调查了培养对ECM修饰的熔体静电纺丝聚己内酯支架生物活性的影响。将成骨细胞接种到支架上并培养1、2或4周,以促进骨特异性ECM沉积,随后进行脱细胞处理以形成无细胞ECM修饰支架。使用温和的化学试剂和脱氧核糖核酸酶在去除DNA的同时高效地保留了ECM的结构和组成。在培养的第一周内观察到熔体静电纺丝纤维上有ECM修饰,在培养2周和4周时ECM增加。较长的培养时间会阻碍重新接种的细胞浸润以及啮齿动物颅骨模型中的整体骨再生。因此,证明培养时间对脱细胞ECM修饰支架的成骨特性有关键影响,长期培养(2周以上)会导致孔隙堵塞并形成干扰骨形成的物理屏障。这些发现对开发用于骨再生的有效ECM修饰支架具有重要意义。

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