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作 者:李焱[1] 张杰[1] 武赟[1] 杨劲[2] 杨珂[2] 郭海英[2]
机构地区:[1]第三军医大学学员旅五队,重庆400038 [2]第三军医大学基础部细胞生物学教研室,重庆400038
出 处:《现代生物医学进展》2013年第35期6848-6851,6936,共5页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(81101205);本科生教学改革课题(2011B11)
摘 要:目的:探讨分泌性的糖蛋白Wnt5a对永生化小鼠黑素细胞系melan-a细胞产黑素的影响。方法:用带有Wnt5a基因的腺病毒及对照组腺病毒作为载体感染体外培养的melan-a黑素细胞;MTT法测定细胞增殖率;体外氧化DOPA反应法测定酪氨酸酶活性;NaOH法测定黑素含量;RT-PCR方法检测melan-a细胞中MITF的表达。结果:与AdGFP对照组相比,AdWnt5a处理组melan-a细胞的增殖率明显降低(P<0.01);DOPA反应法和NaOH法检测结果发现,Wnt5a能显著降低melan-a细胞内酪氨酸酶活性(P<0.01)以及黑素含量(P<0.05);RT-PCR结果表明,Wnt5a显著下调melan-a细胞内MITF的表达(P<0.01)。结论:以上结果显示,AdWnt5a处理组melan-a细胞的增殖率、酪氨酸酶活性、产黑素的量及MITF的表达均有所下降。实验结果提示,Wnt5a能有效抑制melan-a细胞产黑素的能力,并且其作用机制可能与下调MITF的表达有关。Objective: To investigate the effect of Wnt5a on the Melanogenesis of Melan-a cells. Methods: Cultured melan-a melanocytes in vitro were infected by the adenovirus with Wnt5a gene; MTT method was used for determination of cell proliferation rate; Tyrosinase activity assays were performed by the method of DOPA; NaOH method was used for determination of melanin content; The expression of MITF in melan-a melanocytes was performed by reverse transcription-polymerase chain reaction (RT-PCR). Results: Compared with AdGFP, the proliferation rate of AdWnt5a-infected melan-a cells reduced significantly (P〈0.01). DOPA and NaOH assay revealed that Wnt5a significantly inhibited the activity of tyrosianse (P〈0.01) and melanin content (P〈0.05) in melan-a cells. Furthermore, RT-PCR analysis showed that Wnt5a downregulated the expression of MITF in melan-a cells (P〈0.01). Conclusion: Collectively, it is demonstrated that Wnt5a inhibited the proliferation, downregulated the activity of tyrosinase, the melanin content and the expression level of MITF in melan-a cells. The results suggested that Wnt5a contributed to inhibit the melanin synthesis through downgulating the expression of MITF in melan-a cells.
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