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小型猪富血小板血浆对牙周膜干细胞的成骨诱导
引用本文:张远,钟良军,张鹏涛,张源明,徐艳.小型猪富血小板血浆对牙周膜干细胞的成骨诱导[J].中国临床康复,2012(1):125-129.
作者姓名:张远  钟良军  张鹏涛  张源明  徐艳
作者单位:[1]新疆医科大学第一附属医院口腔系,新疆维吾尔自治区乌鲁小齐市830011 [2]杭州师范大学临床医学院,浙江省杭州市310015 [3]新疆医科大学第一附属医院心脏中心,新疆维吾尔自治区乌鲁木齐市830054 [4]南京医科欠学附属口腔医院,江苏省南京市210029
基金项目:自治区科技支疆项目(201091144)
摘    要:背景:组织工程技术为牙周炎致骨组织缺损的修复提供了新的思路。目的:探寻富血小板血浆在小型猪牙周膜干细胞成骨诱导中的作用。方法:采集贵州小型猪静脉血,三次离心制备富血小板血浆。采用组织块法分离培养小型猪牙周膜干细胞,分别将含体积分数0.8%,1.0%,1.2%的富血小板血浆与牙周膜干细胞共同培养3,7,14,21d,以未添加富血小板血浆的牙周膜干细胞作为对照。结果与结论:体积分数0.8%,1.0%,1.2%的富血小板血浆成骨诱导第14天,碱性磷酸酶活性达到峰值,其中体积分数1.0%的富血小板血浆诱导的细胞碱性磷酸酶活性最高,第21天时碱性磷酸酶活性降低。茜素红染色显示富血小板血浆成骨诱导第21天细胞染色呈阳性。单克隆纯化后细胞的生长曲线从第3天起进入对数生长期,第8天细胞数量达到顶峰。说明富血小板血浆具有诱导牙周膜干细胞成骨的能力,以体积分数1.0%时诱导成骨效率最优。

关 键 词:牙周膜干细胞  小型猪  富血小板血浆  成骨诱导  碱性磷酸酶

Effect of miniature pig platelet-rich plasma on osteogenic induction of periodontal ligament stem cells in vitro
Zhang Yuan,Zhong Liang-jun,Zhang Peng-tao,Zhang Yuan-ming,Xu Yan.Effect of miniature pig platelet-rich plasma on osteogenic induction of periodontal ligament stem cells in vitro[J].Chinese Journal of Clinical Rehabilitation,2012(1):125-129.
Authors:Zhang Yuan  Zhong Liang-jun  Zhang Peng-tao  Zhang Yuan-ming  Xu Yan
Institution:1Department of Stomatology, the First Affiliated Hospital of Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China; 2Clinical Medical College of Hangzhou Normal University, Hangzhou 310015, Zhejiang Province, China; 3Heart Center, the First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, Xinjiang Uygur Autonomous Region, China; 4 Affiliated Dental Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China
Abstract:BACKGROUND: Tissue engineering technology provides a new way for bone defects caused by periodontitis. OBJECTIVE: To explore the effect of platelet-rich plasma (PRP) on osteogenic induction of miniature pig periodontal ligament stem cells (PDLSCs). METHODS: Collected the Guizhou miniature pig’s venous blood and prepared the centrifuged PRP three times; tissue block method was used to culture the periodontal ligament cells. 0.8%, 1.0%, 1.2% concentration of PRP were co-cultured with PDLSCs for 3, 7, 14 and 21 days, respectively. No PRP addition as control group. RESULTS AND CONCLUSION: Alkaline phosphatase (AKP) activity reach a peak at the 14th day after induced with 0.8%, 1.0% and 1.2% PRP, and highest activity of AKP was induced by 1.0% PRP. AKP activity was reduced at the 21st day. Alizarin red staining showed the PDLSCs were positive at 21st day after osteogenic induction of PRP. Purified monoclonal cell growth curve entering the logarithmic growth phase since the 3rd day, the amount of cells reached a peak at the 8th day. PRP can induce osteogenic PDLSC performance, especially the 1.0% PRP induction showed the optimal efficiency in vitro.
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