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作 者:王悦[1] 朱喆[2] 成荣杰[3] 张丽红[4] 马英智[5] 周延民[1]
机构地区:[1]吉林大学口腔医院种植中心,长春130021 [2]吉林大学前卫医院病理科 [3]哈尔滨医科大学第四临床医院妇产科 [4]吉林大学白求恩医学院病理系 [5]空军航空大学培训基地门诊部
出 处:《实用口腔医学杂志》2012年第1期64-69,共6页Journal of Practical Stomatology
基 金:吉林省科学技术厅项目(编号:200804423)
摘 要:目的:研究富血小板血浆(PRP)对人真皮成纤维细胞(hFbs)增殖、分化及胞质中PDGF、TGF-β和VEGF表达量的影响。方法:2次离心法制备PRP,成骨诱导条件下hFbs培养液中加入不同浓度PRP于第12天、21天钙-钴法染色,第21天茜素红染色;免疫细胞化学法检测加不同浓度PRP后第4天细胞PDGF、TGF-β和VEGF的表达;碱性磷酸酶染色(ALP)检测细胞活性;CCK-8法检测有和无成骨诱导条件下不同浓度PRP对细胞增殖的影响。结果:茜素红染色显示,2.8%PRP组钙结节形成最明显;钙-钴法染色显示,2.8%PRP组矿化作用最强;免疫细胞化学结果表明PDGF表达存在剂量依赖性,TGF-β和VEGF表达虽无剂量依赖性,但有适宜浓度的要求;ALP染色表明3%PRP组细胞增殖明显,活性最强。CCK-8检测表明各浓度PRP对hFbs均有促增殖作用,PRP加成骨诱导组比单纯PRP组表现出更明显的促增殖作用,其中4.8%PRP促增殖作用最强。结论:适宜浓度的PRP可促进hFbs增殖,但相关因子的表达存在适宜浓度的要求,PRP通过促进细胞增殖,增加相关因子表达促进创伤愈合。Objective: To study the effects of platelet-rich plasma(PRP) on the proliferation and differentiation of human dermal fibroblasts(hFbs) and on the expression of platelet-derived growth factor(PDGF),transforming growth factor(TGF-β) and vascular endothelial growth factor(VEGF) in hFbs.Methods: PRP was prepared by twice centrifugation method.hFbs were treated by different concentrations of PRP and cultured under osteogenesis induction medium.The mineralization of the hFbs was examined by calcium-cobalt staining and the alizarin red staining at 12 d and 21 d.The expression of PDGF,TGF-β and VEGF was evaluated by immunocytochemistry,alkaline phosphatase(ALP) expression was tested by ALP staining,cell proliferation was detected by CCK-8 assay.Results: The formation of calcium node in 2.8%PRP group in mineralization induction culture was significant.The expression of PDGF was PRP dose-dependence,but TGF-β and VEGF expression needed an appropriate PRP concentration.ALP expression increased in 3% PRP group significantly.Proliferation of hFbs in mineralization induction culture was increased more.Conclusion: PRP may promote the proliferation,differentiation and relative growth factor expression of hFbs.
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