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机构地区:[1]第四军医大学口腔医学院,陕西西安710032
出 处:《牙体牙髓牙周病学杂志》2005年第8期424-427,共4页Chinese Journal of Conservative Dentistry
基 金:第四军医大学创新工程重点课题(CX02F002)
摘 要:目的:了解体外研究环境中,两种不同形式釉基质蛋白(粗提型EMPs和纯化型EMD)对外胚间充质细胞黏附、伸展行为的影响力。方法:酶消化法培养SD大鼠颌突外胚间充质细胞,采用固相结合分析方法,观察外胚间充质细胞在不同浓度釉基质蛋白(50、100、150及200μg/mL等浓度的EMPs和EMD)包被的培养孔表面黏附、伸展情况,依次命名为ED1、ED2、ED3、ED4及EP1、EP2、EP3、EP4组。结果:①细胞黏附性实验中,仅ED2和ED3组结果高于空白对照组(P<0.01)。②细胞伸展实验中,EP1、EP2和EP3组结果高于空白对照组(P<0.01)。结论:EMD对外胚间充质细胞伸展无明显促进作用,但可显著促进其黏附贴壁;EMPs对外胚间充质细胞黏附无影响,但可促进其伸展。AIM:To compare and determine the ability of enamel matrix proteins (EMPs & EMD) to influence specific properties of attachment and spreading of rat ectomesenchymal stem cells in vitro. METHODS:Cell culture technique and solid - phase hireling assay were used to measure the amount of attached cells and the ratio of spreading cells on the EMPs - or EMD - eoated surface of culture wall, according to the concentration (50,100,150 and 200μg/mL) of protein grouped as EDI , ED2, ED3,ED4及EP1 , EP2, EP3, EP4. RESULTS :①The amount of attached cells in ED2 and ED3 group was higher than that of the negative control ( P 〈0.01 ) ;②The ratio of spread cells in EP1 ,EP2 and EP3 group was higher than that of the negative control (P 〈 0.01 ). CONCLUSION:There are little difference of bioeffect between EMD and EMPs,i. e. EMD can increase the attachment of ectomesenchymal stem cells, EMPs can enhance cell spreading.
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