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作 者:李锋[1] 黄作平[1] 黄学平[1] 王志强[1] 朱梅刚[1] 赵彤[1]
机构地区:[1]南方医科大学基础医学院病理学系,广东广州510515
出 处:《中华肿瘤防治杂志》2014年第3期174-177,182,共5页Chinese Journal of Cancer Prevention and Treatment
基 金:国家自然科学基金(81071941)
摘 要:目的:探究经典型霍奇金淋巴瘤细胞系L428中大小细胞亚系生物学特性差异及其意义。方法:应用有限稀释法分离出L428中大小细胞亚系并进行传代培养,分别命名为L428-big和L428-small细胞。免疫细胞化学实验检测L428中大小细胞亚系CD15和CD30表达差异,MTT实验检测L428中大小细胞亚系增殖能力的差异;流式细胞术检测L428中大小细胞亚系的凋亡差异。结果:成功分离出L428细胞株中大小细胞亚系并进行传代培养;免疫组化显示L428-big细胞的CD15及CD30表达明显强于L428-small细胞;MTT实验显示,L428-big细胞和L428-small细胞之间增殖能力差异有统计学意义,F=565.273,P<0.001,L428-small细胞增殖能力高于L428-big细胞,P<0.001;流式细胞术显示,L428-big细胞的凋亡率为(3.3±0.1)%,明显多于L428-small细胞(0.4±0.1)%,P<0.001。结论:L428-small细胞增殖能力强,凋亡少,为经典型霍奇金淋巴瘤细胞起源的进一步研究提供一定的实验基础。OBJECTIVE:To investigate differences of biological characteristics of big and small cell sublines in classi- cal Hodgkins lymphoma cell lines L428 and its significance. METHODS: Limited diluted method was used to separate the big and small cell sublines apart in cell lines of L428 which were named as L428 big and L428-small cell lines. Immunohis tochemisty was applied to detect the expression of CD15 and CD30 in cell lines of L428-big and L428-small. MTT assay was used to determine the differences of proliferation ability in cell lines of L428-big and L428-smalL Apoptosis was ana- lyzed by flow cytometry in cell lines of L428-big and L428-small. RESULTS: L428 cell lines were successfully separated with cell lines of L428-big and L428-small;Immunohistoehemistry showed the expression of CD15 and CD30 in L428-big cells were significantly stronger than that in L428-small cells;MTT assay showed that the differences between L428-big cells and L428-small cells were statistically significant (F= 565. 273, P〈0. 001), with much higher multiplication capacity in L428-samll cells than that of L428-big cells (P〈0. 001) ;Flow cytometry showed more apoptotic cells in L428-big cells (3.3±0. 1)% than that of L428-small cells(0.4±0. 1)% (P〈0.00l). CONCLUSION: The L428-small cell lines show higher multiplication capacity and less apoptotic cells, which is expected to provide the experimental basis for further study of the origins of classical Hodgkin lymphoma ceils.
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