Paolin Adolfo, Trojan Diletta, Leonardi Antonio, Mellone Stefano, Volpe Antonio, Orlandi Augusto, Cogliati Elisa
Treviso Tissue Bank Foundation, Piazzale Ospedale 1, Via Scarpa 9, 31100, Treviso, Italy.
Department of Molecular Medicine and Biomedical Technologies, Medical School, Federico II University of Naples, Via Pansini 5, 80131, Napoli, Italy.
Cell Tissue Bank. 2016 Sep;17(3):399-406. doi: 10.1007/s10561-016-9553-x. Epub 2016 Apr 12.
The aim of this work was to compare the effects on human amniotic membrane of freeze-drying and γ-irradiation at doses of 10, 20 and 30 kGy, with freezing. For this purpose, nine cytokines (interleukin 10, platelet-derived growth factor-AA, platelet-derived growth factor-BB, basic fibroblast growth factor, epidermal growth factor, transforming growth factor beta 1, and tissue inhibitors of metalloproteinase-1, -2, and -4) were titrated in 5 different preparations for each of 3 amniotic membranes included in the study. In addition, the extracellular matrix structure of each sample was assessed by transmission electron microscopy. While freeze-drying did not seem to affect the biological structure or cytokine content of the different amniotic membrane samples, γ-irradiation led to a significant decrease in the tissue inhibitors of metalloproteinase-4, basic fibroblast growth factor and epidermal growth factor, and induced structural damage to the epithelium, basement membrane and lamina densa. The higher the irradiation dose the more severe the damage to the amniotic membrane structure. In conclusion, the Authors recommend processing amniotic membrane under sterile conditions to guarantee safety at every step rather than final sterilization with γ-irradiation, thereby avoiding alteration to the biological characteristics of the amniotic membrane.
本研究的目的是比较冻干、10、20和30千戈瑞剂量的γ射线辐照以及冷冻对人羊膜的影响。为此,对研究中纳入的3张羊膜各自的5种不同制剂中的9种细胞因子(白细胞介素10、血小板衍生生长因子-AA、血小板衍生生长因子-BB、碱性成纤维细胞生长因子、表皮生长因子、转化生长因子β1以及金属蛋白酶组织抑制剂-1、-2和-4)进行了滴定。此外,通过透射电子显微镜对每个样本的细胞外基质结构进行了评估。虽然冻干似乎并未影响不同羊膜样本的生物学结构或细胞因子含量,但γ射线辐照导致金属蛋白酶组织抑制剂-4、碱性成纤维细胞生长因子和表皮生长因子显著减少,并对上皮、基底膜和致密层造成结构损伤。辐照剂量越高,对羊膜结构的损伤越严重。总之,作者建议在无菌条件下处理羊膜,以确保每一步的安全性,而不是用γ射线辐照进行最终灭菌,从而避免改变羊膜的生物学特性。