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使用具有体内沉积细胞外基质的羟基磷灰石海绵支架进行骨再生

Bone Regeneration Using Hydroxyapatite Sponge Scaffolds with In Vivo Deposited Extracellular Matrix.

作者信息

Ventura Reiza Dolendo, Padalhin Andrew Reyes, Min Young-Ki, Lee Byong-Taek

机构信息

1 Department of Regenerative Medicine, College of Medicine, Soonchunhyang University , Cheonan, Republic of Korea.

2 Department of Physiology, College of Medicine, Soonchunhyang University , Cheonan, Republic of Korea.

出版信息

Tissue Eng Part A. 2015 Nov;21(21-22):2649-61. doi: 10.1089/ten.TEA.2015.0024. Epub 2015 Oct 21.

Abstract

There is currently an increased interest in studying the extracellular matrix (ECM) and its potential applications for tissue engineering and regenerative medicine. The ECM plays an important role by providing adhesive substrates to cells during migration, morphogenesis, differentiation, and homeostasis by signaling biochemical and biomechanical cues to cells. In this study, the ECM was incorporated into hydroxyapatite by implanting sponge replica scaffolds in subcutaneous pockets in rats, and the implants were tested for bone regeneration potential. The resulting scaffolds were characterized using scanning electron microscopy, confocal microscopy, DNA and RNA quantification, tissue staining, energy dispersive X-ray spectroscopy analysis, compressive strength testing, porosity, and pore size distribution analysis using bare scaffolds as a control reference. Biocompatibility was assessed using MC3T3-E1 preosteoblast cells and in vivo studies were carried out by implanting decellularized scaffolds in 11 mm radial defects in New Zealand rabbits for 4 and 8 weeks to determine the effect of the in vivo deposited ECM. Material characterization indicated that a 2-week decellularized scaffold was the best among the samples, with an evenly distributed ECM visible on hematoxylin and eosin-stained tissue sections, a compressive strength of 2.53 ± 0.68 MPa, a porosity of 58.08 ± 3.32% and a pore size distribution range of 10-150 μm. In vivo results showed no severe inflammation, with increased cell infiltration followed by dense matrix deposition after 4 weeks and new bone formation at 8 weeks. The results indicate that incorporation of an in vivo deposited ECM into ceramic scaffolds can potentially improve bone regeneration.

摘要

目前,人们对研究细胞外基质(ECM)及其在组织工程和再生医学中的潜在应用兴趣日益浓厚。ECM通过在细胞迁移、形态发生、分化和内环境稳定过程中向细胞传递生化和生物力学信号,为细胞提供黏附底物,发挥着重要作用。在本研究中,通过将海绵复制品支架植入大鼠皮下囊袋,将ECM整合到羟基磷灰石中,并对植入物的骨再生潜力进行测试。使用扫描电子显微镜、共聚焦显微镜、DNA和RNA定量、组织染色、能量色散X射线光谱分析、抗压强度测试、孔隙率以及以裸支架作为对照参考的孔径分布分析等方法对所得支架进行表征。使用MC3T3-E1前成骨细胞评估生物相容性,并通过将去细胞支架植入新西兰兔的11毫米桡骨缺损处4周和8周,进行体内研究,以确定体内沉积ECM的效果。材料表征表明,在样品中,2周的去细胞支架是最佳的,在苏木精和伊红染色的组织切片上可见均匀分布的ECM,抗压强度为2.53±0.68兆帕,孔隙率为58.08±3.32%以及孔径分布范围为10-150微米。体内结果显示无严重炎症,4周后细胞浸润增加,随后有致密基质沉积,8周时有新骨形成。结果表明,将体内沉积的ECM整合到陶瓷支架中可能会改善骨再生。

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