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作 者:毛越苹[1] 齐庆[2] 谭国珍[1] 郭庆[1] 曾凡钦[1]
机构地区:[1]中山大学附属第二医院皮肤性病科,广东广州510120 [2]广州中医药大学附属第一医院皮肤性病科,广东广州510405
出 处:《第四军医大学学报》2009年第17期1587-1590,共4页Journal of the Fourth Military Medical University
摘 要:目的:比较小鼠真皮间充质干细胞(mdMSCs)和人胚胎真皮间充质干细胞(hdMSCs)对人皮肤成纤维细胞(hsFb)组织修复作用的影响,探讨异种属真皮间充质干细胞(MSCs)促进hsFb组织修复的可靠性.方法:采用低血清培养基,以消化—贴壁—传代法体外培养、鉴定mdMSCs和hdM-SCs,并与体外分离培养的hsFb于transwell培养体系中共培养,采用样本碱水解法和ELISA法分别检测第1,4日培养上清液中羟脯氨酸(Hyp)和转化生长因子-β1(TGF-β1)的变化.结果:不同种属MSCs(mdMSCs/hdMSCs)对共培养上清液Hyp含量的影响差异(F=0.174)以及不同处理组(即不同细胞密度MSCs)培养上清液Hyp含量差异(F=1.304)均无显著性.不同时间(即第1和第4日)共培养上清液Hyp含量差异具有统计学意义(F=8.712,P<0.01).不同种属MSCs(mdMSCs/hdMSCs)对上清液TGF-β1的含量影响差异(F=0.062)以及不同处理组(即不同细胞密度MSCs)培养上清液TGF-β1含量差异(F=1.991)均无显著性.不同时间(即第1和第4日)培养上清液TGF-β1含量差异具有统计学意义(F=0.699,P<0.05).结论:不同来源真皮MSCs与hsFb共培养对胶原分泌和TGF-β1表达无影响,组织修复过程中,异种属真皮MSCs的诱导是可靠的.AIM: To compare the tissue repair effect of mouse dermis-derived mesenchymal stem eells(mdMSCs)and human dermis-derived MSCs(hdMSCs) on normal human skin fibroblast (hsFb) and to explore the reliability of heterogeneously dermis-derived MSCs in tissue repair. METHODS: mdMSCs and hdMSCs were isolated and cultivated by tissue digested-adherent-passage in lowserum medium and the changes of hydroxyproline (Hyp) and TGF-β1 were determined in co-culture system of mdMSCs or hdMSCs and hsFb on day 1 and 4 by samples basic hydrolysis and ELISA respectively. RESULTS: No significant difference was found in the contents of Hyp between groups of different MSCs( F = 0. 174) or between groups of different cell density ( F = 1. 304 ). The contents of Hyp were significantly different between day 1 and day 4 ( F = 8. 712, P 〈0.01 ). The level of TGF-β1 was not significantly different between groups of different MSCs( F = 0.062) or between groups of different cell density( F = 1. 991 ). The level of TGF-β1 was significantly different between day 1 and day 4 ( F = 0. 699, P 〈 0. 05 ). CONCLUSION : Dermal MSCs of different origin (mouse or human ) would not affect the levels of collagen and TGF-131 when cultivated with hsFb. It is reliable for heterogeneously dermis-derived MSCs to promote tissue repair on hsFb.
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