Skaalure Stacey C, Chu Stanley, Bryant Stephanie J
Department of Chemical and Biological Engineering, University of Colorado, Boulder, CO, 80309, USA; BioFrontiers Institute, University of Colorado, Boulder, CO, 80309, USA.
Adv Healthc Mater. 2015 Feb 18;4(3):420-31. doi: 10.1002/adhm.201400277. Epub 2014 Oct 8.
A new cartilage-specific degradable hydrogel based on photoclickable thiol-ene poly(ethylene glycol) (PEG) hydrogels is presented. The hydrogel crosslinks are composed of the peptide, CRDTEGE-ARGSVIDRC, derived from the aggrecanase-cleavable site in aggrecan. This new hydrogel is evaluated for use in cartilage tissue engineering by encapsulating bovine chondrocytes from different cell sources (skeletally immature (juvenile) and mature (adult) donors and adult cells stimulated with proinflammatory lipopolysaccharide (LPS)) and culturing for 12 weeks. Regardless of cell source, a twofold decrease in compressive modulus is observed by 12 weeks, but without significant hydrogel swelling indicating limited bulk degradation. For juvenile cells, a connected matrix rich in aggrecan and collagen II, but minimal collagens I and X is observed. For adult cells, less matrix, but similar quality, is deposited. Aggrecanase activity is elevated, although without accelerating bulk hydrogel degradation. LPS further decreases matrix production, but does not affect aggrecanase activity. In contrast, matrix deposition in the nondegradable hydrogels consists of aggrecan and collagens I, II, and X, indicative of hypertrophic cartilage. Lastly, no inflammatory response in chondrocytes is observed by the aggrecanase-sensitive hydrogels. Overall, it is demonstrated that this new aggrecanase-sensitive hydrogel, which is degradable by chondrocytes and promotes a hyaline-like engineered cartilage, is promising for cartilage regeneration.
本文介绍了一种基于可光点击硫醇-烯聚乙二醇(PEG)水凝胶的新型软骨特异性可降解水凝胶。水凝胶交联物由源自聚集蛋白聚糖中聚集蛋白聚糖酶可切割位点的肽CRDTEGE-ARGSVIDRC组成。通过包封来自不同细胞来源(骨骼未成熟(幼年)和成熟(成年)供体以及用促炎脂多糖(LPS)刺激的成年细胞)的牛软骨细胞并培养12周,对这种新型水凝胶在软骨组织工程中的应用进行了评估。无论细胞来源如何,到12周时观察到压缩模量降低了两倍,但水凝胶没有明显肿胀,表明整体降解有限。对于幼年细胞,观察到富含聚集蛋白聚糖和胶原蛋白II的连接基质,但胶原蛋白I和X极少。对于成年细胞,沉积的基质较少,但质量相似。聚集蛋白聚糖酶活性升高,尽管没有加速水凝胶整体降解。LPS进一步降低了基质产生,但不影响聚集蛋白聚糖酶活性。相比之下,不可降解水凝胶中的基质沉积由聚集蛋白聚糖和胶原蛋白I、II和X组成,表明是肥大软骨。最后,聚集蛋白聚糖酶敏感水凝胶在软骨细胞中未观察到炎症反应。总体而言,已证明这种新型聚集蛋白聚糖酶敏感水凝胶可被软骨细胞降解并促进类似透明软骨的工程化软骨,在软骨再生方面具有前景。