Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, 3584 CM Utrecht, The Netherlands.
Department of Orthopaedics, Regenerative Medicine Center, University Medical Center Utrecht, P.O. Box 85500, 3508 GA Utrecht, The Netherlands.
Int J Mol Sci. 2020 Nov 13;21(22):8571. doi: 10.3390/ijms21228571.
Gelatine methacryloyl (GelMA) hydrogels are widely used in studies aimed at cartilage regeneration. However, the endotoxin content of commercially available GelMAs and gelatines used in these studies is often overlooked, even though endotoxins may influence several cellular functions. Moreover, regulations for clinical use of biomaterials dictate a stringent endotoxin limit. We determined the endotoxin level of five different GelMAs and evaluated the effect on the chondrogenic differentiation of equine mesenchymal stromal cells (MSCs). Cartilage-like matrix production was evaluated by biochemical assays and immunohistochemistry. Furthermore, equine peripheral blood mononuclear cells (PBMCs) were cultured on the hydrogels for 24 h, followed by the assessment of tumour necrosis factor (TNF)-α and C-C motif chemokine ligand (CCL)2 as inflammatory markers. The GelMAs were found to have widely varying endotoxin content (two with >1000 EU/mL and three with <10 EU/mL), however, this was not a critical factor determining in vitro cartilage-like matrix production of embedded MSCs. PBMCs did produce significantly higher TNF-α and CCL2 in response to the GelMA with the highest endotoxin level compared to the other GelMAs. Although limited effects on chondrogenic differentiation were found in this study, caution with the use of commercial hydrogels is warranted in the translation from in vitro to in vivo studies because of regulatory constraints and potential inflammatory effects of the content of these hydrogels.
明胶甲基丙烯酰(GelMA)水凝胶广泛应用于软骨再生研究中。然而,在这些研究中使用的商业 GelMA 和明胶的内毒素含量往往被忽视,尽管内毒素可能会影响几种细胞功能。此外,生物材料临床使用的规定要求严格的内毒素限制。我们确定了五种不同 GelMA 的内毒素水平,并评估了其对马间充质基质细胞(MSCs)的软骨分化的影响。通过生化分析和免疫组织化学评估软骨样基质的产生。此外,将马外周血单核细胞(PBMC)在水凝胶上培养 24 小时,然后评估肿瘤坏死因子(TNF)-α和 C-C 基序趋化因子配体(CCL)2 作为炎症标志物。发现 GelMA 具有广泛变化的内毒素含量(两种含量>1000 EU/mL,三种含量<10 EU/mL),然而,这不是决定嵌入 MSC 体外软骨样基质产生的关键因素。与其他 GelMA 相比,PBMC 对具有最高内毒素水平的 GelMA 产生的 TNF-α和 CCL2 明显更高。尽管在这项研究中发现对软骨分化的影响有限,但由于监管限制和这些水凝胶的潜在炎症作用,从体外到体内研究的转化中使用商业水凝胶时需要谨慎。