摘要
目的:观察改良HBSS液对体外培养人牙周膜细胞(PDLCs)增殖活性的影响。方法:在添加青霉素、链霉素各100U/ml、地塞米松8 mg/L的HBSS液中分别加入1、3和5 mmol/L的还原型谷胱甘肽(GSH)制成改良HBSS液,并与HBSS液、HC-A离体肾保存液及蒸馏水比较,用MTS法测定培养第4代PDLCs在上述溶液中保存不同时间后的增殖活性。结果:HBSS液组和改良HBSS液组在0.5~48h的PDLCs增殖活性显著高于HC-A液组和蒸馏水组(后两者之间没有显著差异),而改良HBSS液含3 mmol/L GSH组和5 mmol/L GSH组在2~12 h显著高于HBSS液组,1 mmol/L GSH组在2~6 h显著高于HBSS液组,5 mmol/L GSH组在2~12 h显著高于含GSH的其它浓度组。结论:改良HBSS液保存人PDLCs增殖活性的效果好于HBSS液,其中含5 mmol/L GSH的改良液在12 h内的效果最好。
Objective: To study the effectiveness of modified Hankg balanced salt solution (HBSS) on the proliferation of human periodontal ligament cells (PDLCs) in vitro at room temperature. Methods: Human PDLCs were cultured in vitro. The modified HB- SS was prepared by adding 1 mmol/L,3 mmol/L or 5 mmol/L glutathione(GSH) into the HBSS in which 8 mg/L dexamethasone, penicillin and streptomycin at 100 U/ml of each were included. The cells of passage 4 were cultured in the modified HBSS, HC-A kidney preservation solution (HC-A) and distilled water( H2 O) for 0. 5 ,1,2 ,6 ,12 ,24 and 48 h respectively. The proliferation of the cells was examined by MTS assay. Results : From 0.5- 48 h, the proliferation activity of PDLCs in HBSS and modified HBSS was significantly higher than in HC- A and H2O ( HC - A vs H2O, P 〉 0.05 ), that in 3 mmol/L GSH and 5 mmol/L GSH was significant- ly higher than in HBSS from 2 - 12 h, in 1 mmol/L GSH was significantly higher than in HBSS from 2 - 6 h, and in 5 mmol/L GSH was significantly higher than in other media containing GSH from 2 - 12 h. Conclusion: Adding GSH into HBSS can improve the ef- fectiveness for human PDLC proliferation, modified HBSS with 5 mmol/L GSH is suitable for 12 hour human PDLCs storage.
出处
《实用口腔医学杂志》
CAS
CSCD
北大核心
2013年第3期385-388,共4页
Journal of Practical Stomatology
基金
国家自然科学基金(编号:30900860)
关键词
牙脱位
牙周膜
谷胱甘肽
器官保存液
Tooth avulsion
Periodontal ligament
Glutathione
Organ preservation solutions