人牙周膜的生化研究:脉冲电磁场诱导细胞附着材料的制备。

K T Kim
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引用次数: 0

摘要

牙周组织,尤其是牙周韧带和牙槽骨,是经常受到诸如咬合和咀嚼等物理压力的组织。本实验旨在探讨脉冲电磁场(PEMF)对人牙周韧带成纤维细胞(HPLF)和大鼠成骨细胞(ROB)细胞附着和扩散的影响。PEMF被归类为一种机械应力。采用Saito等人描述的外植体方法获得高通量光子晶体。然后在Dulbecco改良Eagle培养基(D-MEM)中继代培养,胰蛋白酶化后添加2 mg/ml透析胎牛血清蛋白(FCSP)、50微克/ml抗坏血酸和青霉素/链霉素。采用Dziak和Brand描述的顺序细菌胶原酶消化法从2日龄大鼠颅骨中分离出ROB,并在添加FCSP、抗坏血酸和青霉素/链霉素的D-MEM中传代培养。将融合HPLF与无血清MCDB 107培养基培养后,静息HPLF分别在加或不加PEMF的情况下暴露24小时。随后收集对照条件培养基(C-CM)和PEMF暴露条件培养基(PEMF- cm)。用PO-60K色谱柱包被整个条件培养基或分离条件培养基,进行细胞贴壁实验。包被后,热失活的BSA阻断非特异性位点的细胞粘附,3H-TdR标记的HPLF或ROB在预包被的孔上培养。用闪烁计数器测定3H-TdR的放射性,测定细胞附着和扩散的活性。由HPLF衍生的细胞附着因子具有疏水、热不稳定和蛋白水解酶可消化的特点。此外,分离的PEMF-CM增强了ROB的扩散活性。PEMF诱导了10 KDa,增强了HPLF和ROB的扩散。因此,暴露于PEMF的HPLF分泌的细胞附着因子和扩散因子可能调控HPLF和ROB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biochemical study of human periodontal ligament: preparation of cell attachment materials induced by pulsed electromagnetic fields.

The periodontium, especially the periodontal ligament and alveolar bone, are tissues constantly subjected to physical stress such as occlusion and mastication. This study was designed to explore the effect of the pulsed electromagnetic fields (PEMF) on the cell attachment and the spread of human periodontal ligament fibroblasts (HPLF) and rat osteoblasts (ROB). PEMF are categorized as one type of mechanical stress. HPLF were obtained by the explantation method described by Saito et al. They were then subcultured in Dulbecco's modified Eagle's medium (D-MEM) and supplemented with 2 mg/ml dialyzed fetal calf serum protein (FCSP), 50 micrograms/ml ascorbic acid and penicillin/streptomycin after trypsinization. ROB were isolated from a two-day-old rat calvaria by the sequential bacterial collagenase digestion method described by Dziak and Brand and were subcultured in D-MEM supplemented with FCSP, ascorbic acid and penicillin/streptomycin. After the confluent HPLF were cultured with serum-free MCDB 107 medium, the quiescent HPLF were exposed with or without PEMF for 24 hr. This was followed by the collection of the control conditioned medium (C-CM) and PEMF exposed conditioned medium (PEMF-CM). The cell attachment assay was performed so that the hydrophobic 24 multiwells were coated with the whole conditioned medium or fractionated conditioned medium by a PO-60K column. After coating, heat inactivated BSA blocked nonspecific sites for cell adhesion, and 3H-TdR labeled HPLF or ROB were cultured on the precoated wells. The activity of cell attachment and spreading was determined by the radioactivity of 3H-TdR using a scintillation counter. The characters of cell attachment factors derived from HPLF were hydrophobic, heat labile and proteolytic enzyme digestible. In addition, the fractionated PEMF-CM enhanced the spreading activity of ROB. PEMF induced the 10 KDa which can enhance the HPLF and ROB spreading. Therefore, the cell attachment and spreading factors secreted by HPLF exposed with PEMF may regulate HPLF and also ROB.

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