首页> 外文期刊>Journal of Immunological Methods >A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V.
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A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V.

机译:一种凋亡的新测定法。使用荧光素标记的膜联蛋白V流式细胞术检测早期凋亡细胞上磷脂酰丝氨酸的表达。

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In the early stages of apoptosis changes occur at the cell surface, which until now have remained difficult to recognize. One of these plasma membrane alterations is the translocation of phosphatidylserine (PS) from the inner side of the plasma membrane to the outer layer, by which PS becomes exposed at the external surface of the cell. Annexin V is a Ca2+ dependent phospholipid-binding protein with high affinity for PS. Hence this protein can be used as a sensitive probe for PS exposure upon the cell membrane. Translocation of PS to the external cell surface is not unique to apoptosis, but occurs also during cell necrosis. The difference between these two forms of cell death is that during the initial stages of apoptosis the cell membrane remains intact, while at the very moment that necrosis occurs the cell membrane looses its integrity and becomes leaky. Therefore the measurement of Annexin V binding to the cell surface as indicative for apoptosis has to be performed in conjunction with a dye exclusion test to establish integrity of the cell membrane. This paper describes the results of such an assay, as obtained in cultured HSB-2 cells, rendered apoptotic by irradiation and in human lymphocytes, following dexamethasone treatment. Untreated and treated cells were evaluated for apoptosis by light microscopy, by measuring the amount of hypo-diploid cells using of DNA flow cytometry (FCM) and by DNA electrophoresis to establish whether or not DNA fragmentation had occurred. Annexin V binding was assessed using bivariate FCM, and cell staining was evaluated with fluorescein isothiocyanate (FITC)-labelled Annexin V (green fluorescence), simultaneously with dye exclusion of propidium iodide (PI) (negative for red fluorescence). The test described, discriminates intact cells (FITC-/PI-), apoptotic cells (FITC+/PI-) and necrotic cells (FITC+/PI+). In comparison with existing traditional tests the Annexin V assay is sensitive and easy to perform. The Annexin V assay offers the possibility of detecting early phases of apoptosis before the loss of cell membrane integrity and permits measurements of the kinetics of apoptotic death in relation to the cell cycle. More extensive FCM will allow discrimination between different cell subpopulations, that may or may not be involved in the apoptotic process.
机译:在细胞凋亡的早期阶段,变化发生在细胞表面,直到现在仍然难以识别。这些质膜改变之一是磷脂酰丝氨酸(PS)从质膜的内侧到外层的移位,由此PS暴露于细胞的外表面。膜联蛋白V是对PS具有高亲和力的Ca 2+依赖性磷脂结合蛋白。因此,该蛋白可用作在细胞膜上暴露PS的敏感探针。 PS向细胞外表面的转运不是细胞凋亡独有的,而是在细胞坏死过程中也发生。两种形式的细胞死亡之间的区别在于,在细胞凋亡的初始阶段,细胞膜保持完好无损,而在发生坏死的那一刻,细胞膜就会失去完整性并渗漏。因此,必须结合染料排阻测试来进行膜联蛋白V与细胞表面结合的测量以指示细胞凋亡,以建立细胞膜的完整性。本文描述了在地塞米松治疗后,在培养的HSB-2细胞中通过辐射使细胞凋亡以及在人淋巴细胞中获得的这种检测结果。通过光学显微镜,通过使用DNA流式细胞仪(FCM)测量次二倍体细胞的数量以及通过DNA电泳确定未处理的细胞和未处理的细胞的凋亡来进行评估。使用双变量FCM评估膜联蛋白V的结合,并用异硫氰酸荧光素(FITC)标记的膜联蛋白V(绿色荧光)评估细胞染色,同时用染料排除碘化丙啶(PI)(红色荧光阴性)。所描述的测试可区分完整细胞(FITC- / PI-),凋亡细胞(FITC + / PI-)和坏死细胞(FITC + / PI +)。与现有的传统测试相比,Annexin V检测灵敏且易于执行。膜联蛋白V测定法提供了在细胞膜完整性丧失之前检测凋亡早期的可能性,并允许测量与细胞周期有关的凋亡死亡动力学。更广泛的FCM将允许区分不同的细胞亚群,这些亚群可能或可能不参与凋亡过程。

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