Tissue Engineering 3D-Printed Scaffold Using Allograft/Alginate/Gelatin Hydrogels Coated With Platelet-Rich Fibrin or Adipose Stromal Vascular Fraction Induces Osteogenesis In Vitro

IF 4.5 2区 生物学 Q2 CELL BIOLOGY Journal of Cellular Physiology Pub Date : 2024-12-19 DOI:10.1002/jcp.31497
Sahar Baniameri, Hossein Aminianfar, Niusha Gharehdaghi, Amir-Ali Yousefi-Koma, Sadra Mohaghegh, Hanieh Nokhbatolfoghahaei, Arash Khojasteh
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Abstract

Incorporating autologous patient-derived products has become imperative to enhance the continually improving outcomes in bone tissue engineering. With this objective in mind, this study aimed to evaluate the osteogenic potential of 3D-printed allograft-alginate-gelatin scaffolds coated with stromal vascular fraction (SVF) and platelet-rich fibrin (PRF). The primary goal was to develop a tissue-engineered construct capable of facilitating efficient bone regeneration through the utilization of biomaterials with advantageous properties and patient-derived products. To achieve this goal, 3D-printed gelatin, allograft, and alginate scaffolds were utilized, along with stem cells derived from the buccal fat pad and human-derived components (PRF, SVF). Cells were seeded onto scaffolds, both with and without SVF/PRF, and subjected to comprehensive assessments including adhesion, proliferation, differentiation (gene expression and protein secretion levels), penetration, and gene expression analysis over 14 days. The data was reported as mean ± standard deviation (SD). Two-way or one-way analysis of variance (ANOVA) was performed, followed by a Tukey post hoc test for multiple comparisons. Statistical significance was determined as a p value below 0.05. The scaffolds demonstrated structural integrity, and the addition of PRF coatings significantly enhanced cellular adhesion, proliferation, and differentiation compared to other groups. Gene expression analysis showed increased expression of osteogenic and angiogenic markers in the PRF-coated scaffolds. These findings highlight the promising role of PRF-coated scaffolds in promoting osteogenesis and facilitating bone tissue regeneration. This study emphasizes the development of patient-specific tissue-engineered constructs as a valuable approach for effective bone regeneration.

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组织工程3d打印支架使用同种异体移植物/海藻酸盐/明胶水凝胶包被富含血小板的纤维蛋白或脂肪基质血管部分诱导体外成骨。
结合患者自身来源的产品已成为当务之急,以提高骨组织工程的持续改善的结果。考虑到这一目标,本研究旨在评估涂有基质血管分数(SVF)和富血小板纤维蛋白(PRF)的3d打印同种异体海藻酸盐-明胶支架的成骨潜力。主要目标是开发一种组织工程结构,能够通过利用具有优势特性的生物材料和患者衍生产品来促进有效的骨再生。为了实现这一目标,使用了3d打印的明胶、同种异体移植物和海藻酸盐支架,以及来自颊脂肪垫和人源性成分(PRF, SVF)的干细胞。将细胞播种到支架上,无论是否含有SVF/PRF,并在14天内进行综合评估,包括粘附、增殖、分化(基因表达和蛋白分泌水平)、渗透和基因表达分析。数据以均数±标准差(SD)报告。进行双向或单向方差分析(ANOVA),然后进行多重比较的Tukey事后检验。以p值< 0.05为差异有统计学意义。支架结构完整,与其他组相比,PRF涂层的添加显著增强了细胞粘附、增殖和分化。基因表达分析显示,prf包被支架中成骨和血管生成标志物的表达增加。这些发现突出了prf包被支架在促进骨生成和促进骨组织再生方面的重要作用。本研究强调患者特异性组织工程结构的发展是有效骨再生的一种有价值的方法。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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