Zhang Naili, Zhou Mo, Zhang Yumin, Wang Xusheng, Ma Shaoying, Dong Li, Yang Ting, Ma Lina, Li Baoxing
School of Basic Medical Science, Southern Medical University, TongHe, GuangZhou, GuangDong, 510515, China.
Cell Tissue Bank. 2014 Sep;15(3):357-67. doi: 10.1007/s10561-013-9391-z. Epub 2013 Aug 17.
Defatting is an important procedure for the preparation of bone grafts because lipids in bone grafts strongly influence the osteointegration. Lipases have been widely used in different fields. However, study on the application to defatting process for bone grafts preparation has never been found so far. In this study, bone samples were treated respectively by lipase, NaHCO(3)/Na(2)CO(3), acetone and deionized water. The lipids content of processed bone grafts was calculated in Soxhlet extractor method. Surface morphology of the bone grafts was observed under scanning electron microscope (SEM). DNA content of processed bone grafts was measured. Cytocompatibility was evaluated by co-culturing mouse preosteoblasts (MC3T3-E1) on defatted bone cubes. Proliferation rates of MC3T3-E1 were examined by cell counting kit-8 (CCK-8) assay. No statistically significant difference was found between lipids amount of bone processed by lipase (0.46 ± 0.16 %) and acetone (1.11 ± 0.13 %) (P > 0.05). Both of them were significantly lower than that in groups processed by Na(2)CO(3)/NaHCO(3) (3.46 ± 0.69 %) and deionized water (8.88 ± 0.18 %) (P = 0.000). Only cell debris were discovered over the surface of bone processed by lipase or acetone, while lipid droplets were observed on bone processed by Na(2)CO(3)/NaHCO(3) or water by SEM. The difference of DNA concentration between the bone processed by lipase (3.16 ± 0.81 ng/μl) and acetone (4.14 ± 0.40 ng/μl) is not statistically significant (P > 0.05). Both of them are significantly lower than that groups processed by Na(2)CO(3)/NaHCO(3) (5.22 ± 0.38 ng/μl) and water (7.88 ± 0.55 ng/μl) (P < 0.05). MC3T3-E1 cells maintained their characteristic spreading on the trabecular surfaces of bone processed by lipase. There were no statistically significant differences among absorbance of lipase, acetone groups in CCK-8 assay. The application of lipase to bone tissue defatting appears to be a very promising technique for bone grafts preparation.
脱脂是制备骨移植材料的重要步骤,因为骨移植材料中的脂质会强烈影响骨整合。脂肪酶已在不同领域广泛应用。然而,迄今为止尚未发现有关其在骨移植材料制备脱脂过程中应用的研究。在本研究中,分别用脂肪酶、NaHCO₃/Na₂CO₃、丙酮和去离子水处理骨样本。采用索氏提取法计算处理后骨移植材料的脂质含量。在扫描电子显微镜(SEM)下观察骨移植材料的表面形态。测定处理后骨移植材料的DNA含量。通过将小鼠前成骨细胞(MC3T3-E1)与脱脂骨块共培养来评估细胞相容性。采用细胞计数试剂盒-8(CCK-8)法检测MC3T3-E1的增殖率。脂肪酶处理的骨(0.46±0.16%)和丙酮处理的骨(1.11±0.13%)的脂质含量之间无统计学显著差异(P>0.05)。它们均显著低于Na₂CO₃/NaHCO₃处理组(3.46±0.69%)和去离子水处理组(8.88±0.18%)(P = 0.000)。在脂肪酶或丙酮处理的骨表面仅发现细胞碎片,而通过SEM观察到在Na₂CO₃/NaHCO₃或水处理的骨上有脂滴。脂肪酶处理的骨(3.16±0.81 ng/μl)和丙酮处理的骨(4.14±0.40 ng/μl)之间的DNA浓度差异无统计学意义(P>0.05)。它们均显著低于Na₂CO₃/NaHCO₃处理组(5.22±0.38 ng/μl)和水处理组(7.88±0.55 ng/μl)(P<0.05)。MC3T3-E1细胞在脂肪酶处理的骨小梁表面保持其特征性铺展。在CCK-8检测中,脂肪酶组和丙酮组的吸光度之间无统计学显著差异。脂肪酶在骨组织脱脂中的应用似乎是一种非常有前景的骨移植材料制备技术。