Chondrogenic potential of PMSCs cultured on chondroitin sulfate/gelatin-modified DBM scaffold.

IF 2.2 4区 工程技术 Q3 PHARMACOLOGY & PHARMACY
Bioimpacts Pub Date : 2024-10-27 eCollection Date: 2025-01-01 DOI:10.34172/bi.2023.30003
Fatemeh Haghwerdi, Ismaeil Haririan, Masoud Soleimani
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引用次数: 0

Abstract

Introduction: Osteoarthritis is one of the most common orthopedic diseases that gradually causes wear and damage to the articular Subchondral bone due to the destruction of articular cartilage. One of the basic challenges in cartilage tissue engineering is the choice of scaffold. In the design of the cartilage scaffold, it is useful to consider parameters such as porosity, water absorption, high mechanical resistance, biocompatibility, and biodegradability. Therefore, in this study, demineralized bone matrix (DBM), which inherently has these characteristics to some extent, was chosen as the basic scaffold.

Methods: The gelatin/DBM (G/DBM) and the chondroitin sulfate-gelatin/DBM (GCS/DBM) scaffolds were prepared, respectively, by incorporating gelatin or chondroitin sulfate/gelatin solution inside DBM pores, freeze-drying and crosslinking with EDC/NHS. The physicochemical, biological characteristics and chondrogenic potential of scaffolds were studied.

Results: According to the SEM results, the size of the DBM pores in the G/DBM and GCS/DBM scaffolds decreased (from almost 100-1500 µm to less than 200 µm), which reduced cell escape compared to the DBM scaffold. Also, crosslinking the scaffolds has greatly increased their compressive E-modulus (more than 8 times). The cytocompatibility and non- toxicity of all scaffolds were confirmed by acridine orange/ethidium bromide (AO/EB) staining. The evaluation results of chondrogenic differentiation of placenta-derived mesenchymal stem cells (PMSCs) on modified scaffolds, using the real-time PCR method, showed that the presence of CS in the GCS/DBM scaffold improved the expression of chondrogenesis markers such as Aggrecan (AGC) (~4 times) and collagen 2 (COL-2) (~2.2 times) compared to the DBM scaffold. Also, Alcian blue staining and immunohistochemical analyses of the scaffolds showed denser and more coherent GAGs and COL-2 protein synthesis on the GCS/DBM than the G/DBM and DBM scaffolds.

Conclusion: According to the results, the GCS/DBM scaffold can be a suitable scaffold for cartilage tissue engineering.

硫酸软骨素/明胶修饰DBM支架培养PMSCs的成软骨潜能。
骨关节炎是一种最常见的骨科疾病,由于关节软骨的破坏而逐渐引起关节软骨下骨的磨损和损伤。软骨组织工程的基本挑战之一是支架的选择。在软骨支架的设计中,考虑孔隙率、吸水性、高机械阻力、生物相容性和生物降解性等参数是有用的。因此,本研究选择在一定程度上具有这些特性的去矿化骨基质(demineralized bone matrix, DBM)作为基础支架。方法:将明胶或硫酸软骨素/明胶溶液掺入DBM孔内,冷冻干燥后与EDC/NHS交联,分别制备明胶/DBM (G/DBM)和硫酸软骨素-明胶/DBM (GCS/DBM)支架。研究了支架的理化、生物学特性和成软骨潜能。结果:SEM结果显示,与DBM支架相比,G/DBM和GCS/DBM支架中DBM孔的大小减小(从近100-1500µm降至200µm以下),减少了细胞逃逸。交联后支架的压缩e模量大大增加(超过8倍)。用吖啶橙/溴化乙啶(AO/EB)染色证实了支架的细胞相容性和无毒性。利用real-time PCR方法对改性支架上胎盘源间充质干细胞(PMSCs)的成软骨分化评价结果显示,与DBM支架相比,GCS/DBM支架中CS的存在使Aggrecan (AGC)和collagen 2 (COL-2)等成软骨标志物的表达提高了~4倍(~2.2倍)。阿利新蓝染色和免疫组织化学分析显示,GCS/DBM比G/DBM和DBM支架上的GAGs和COL-2蛋白合成更密集、更一致。结论:GCS/DBM支架是一种适合软骨组织工程的支架材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioimpacts
Bioimpacts Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.80
自引率
7.70%
发文量
36
审稿时长
5 weeks
期刊介绍: BioImpacts (BI) is a peer-reviewed multidisciplinary international journal, covering original research articles, reviews, commentaries, hypotheses, methodologies, and visions/reflections dealing with all aspects of biological and biomedical researches at molecular, cellular, functional and translational dimensions.
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