Cartilage-penetrating hyaluronic acid hydrogel preserves tissue content and reduces chondrocyte catabolism

IF 3.1 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Michael A. Kowalski, Lorenzo M. Fernandes, Kyle E. Hammond, Sameh Labib, Hicham Drissi, Jay M. Patel
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引用次数: 6

Abstract

Articular cartilage injuries have a limited healing capacity and, due to inflammatory and catabolic activities, often experience progressive degeneration towards osteoarthritis. Current repair techniques generally provide short-term symptomatic relief; however, the regeneration of hyaline cartilage remains elusive, leaving both the repair tissue and surrounding healthy tissue susceptible to long-term wear. Therefore, methods to preserve cartilage following injury, especially from matrix loss and catabolism, are needed to delay, or even prevent, the deteriorative process. The goal of this study was to develop and evaluate a cartilage-penetrating hyaluronic-acid (HA) hydrogel to improve damaged cartilage biomechanics and prevent tissue degeneration. At time zero, the HA-based hydrogel provided a 46.5% increase in compressive modulus and a decrease in permeability after simulated degeneration of explants (collagenase application). Next, in a degenerative culture model (interleukin-1β [IL-1β] for 2 weeks), hydrogel application prior to or midway through the culture mitigated detrimental changes to compressive modulus and permeability observed in non-treated explants. Furthermore, localized loss of proteoglycan was observed in degenerative culture conditions alone (non-treated), but hydrogel administration significantly improved the retention of matrix elements. Finally, NITEGE staining and gene expression analysis showed the ability of the HA gel to decrease chondrocyte catabolic activity. These results highlight the importance of reinforcing damaged cartilage with a biomaterial system to both preserve tissue content and reduce catabolism associated with injury and inflammation.

软骨穿透透明质酸水凝胶保存组织含量,减少软骨细胞分解代谢
关节软骨损伤具有有限的愈合能力,并且由于炎症和分解代谢活动,经常经历进行性退行性骨关节炎。目前的修复技术通常能在短期内缓解症状;然而,透明软骨的再生仍然是难以捉摸的,这使得修复组织和周围的健康组织都容易受到长期磨损。因此,需要在损伤后保护软骨的方法,特别是防止基质损失和分解代谢,以延缓甚至防止软骨的恶化过程。本研究的目的是开发和评估软骨穿透透明质酸(HA)水凝胶,以改善受损软骨的生物力学和防止组织变性。在时间为零时,ha基水凝胶在模拟外植体变性(胶原酶应用)后,压缩模量增加46.5%,渗透性降低。接下来,在退行性培养模型中(白细胞介素-1β [IL-1β]培养2周),在培养之前或中途应用水凝胶可以减轻未处理的外植体对压缩模量和渗透性的有害变化。此外,仅在退行性培养条件下(未处理)观察到蛋白多糖的局部损失,但水凝胶处理显著改善了基质元素的保留。最后,NITEGE染色和基因表达分析显示HA凝胶能够降低软骨细胞分解代谢活性。这些结果强调了用生物材料系统加强受损软骨的重要性,既可以保护组织含量,又可以减少与损伤和炎症相关的分解代谢。
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来源期刊
CiteScore
7.50
自引率
3.00%
发文量
97
审稿时长
4-8 weeks
期刊介绍: Journal of Tissue Engineering and Regenerative Medicine publishes rapidly and rigorously peer-reviewed research papers, reviews, clinical case reports, perspectives, and short communications on topics relevant to the development of therapeutic approaches which combine stem or progenitor cells, biomaterials and scaffolds, growth factors and other bioactive agents, and their respective constructs. All papers should deal with research that has a direct or potential impact on the development of novel clinical approaches for the regeneration or repair of tissues and organs. The journal is multidisciplinary, covering the combination of the principles of life sciences and engineering in efforts to advance medicine and clinical strategies. The journal focuses on the use of cells, materials, and biochemical/mechanical factors in the development of biological functional substitutes that restore, maintain, or improve tissue or organ function. The journal publishes research on any tissue or organ and covers all key aspects of the field, including the development of new biomaterials and processing of scaffolds; the use of different types of cells (mainly stem and progenitor cells) and their culture in specific bioreactors; studies in relevant animal models; and clinical trials in human patients performed under strict regulatory and ethical frameworks. Manuscripts describing the use of advanced methods for the characterization of engineered tissues are also of special interest to the journal readership.
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