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Fluorescent Probes Detecting the Phagocytic Phase of Apoptosis: Enzyme-Substrate Complexes of Topoisomerase and DNA

机译:检测凋亡的吞噬阶段的荧光探针:拓扑异构酶和DNA的酶-底物复合物。

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摘要

In apoptosis, the initial self-driven suicide phase generates cellular corpses which are digested in the phagolysosomes of professional and amateur phagocytes during the subsequent waste-management phase. This ensures the complete elimination of the genetic material which often contains pathological, viral or cancerous DNA sequences. Although the phagocytic phase is critical for the efficient execution of apoptosis, there are currently few methods specifically adapted for its detailed visualization in the fixed tissue section format. To resolve this we developed new fluorescent probes for in situ research. The probes selectively visualize active phagocytic cells of any lineage (professional, amateur phagocytes or surrounding tissue cells) which engulf and digest apoptotic cell DNA. These fluorescent probes are the covalently-bound enzyme-DNA intermediates produced in a topoisomerase reaction with specific “starting” oligonucleotides. They detect a specific marker of DNase II cleavage activity, which occurs exclusively in phagolysosomes of the cells that engulfed apoptotic nuclei. The probes provide snap-shot images of the digestion process occurring in cellular organelles responsible for the actual execution of phagocytic degradation of apoptotic cell corpses. We applied the probes for visualization of the phagocytic reaction in tissue sections of normal thymus and in several human lymphomas. We also discuss the nature, stability and properties of DNase II-type breaks as a marker of phagocytic activity. This development provides a useful fluorescent tool for studies of pathologies where clearance of dying cells is essential, such as cancers, inflammation, infection and auto-immune disorders.
机译:在细胞凋亡中,最初的自我驱动的自杀阶段会产生细胞尸体,这些尸体会在随后的废物管理阶段中在专业吞噬细胞和业余吞噬细胞的吞噬体中被消化。这样可确保完全消除通常包含病理,病毒或癌性DNA序列的遗传物质。尽管吞噬期对于有效执行细胞凋亡至关重要,但目前很少有方法专门适用于固定组织切片形式的详细可视化。为了解决这个问题,我们开发了用于原位研究的新型荧光探针。探针可以选择性吞噬吞噬和消化凋亡细胞DNA的任何谱系的活跃吞噬细胞(专业,业余吞噬细胞或周围组织细胞)。这些荧光探针是在拓扑异构酶反应中与特定的“起始”寡核苷酸产生的共价结合酶-DNA中间体。他们检测到特定的DNase II切割活性标记,该标记仅在吞噬凋亡核的细胞的吞噬体中发生。这些探针提供了发生在细胞器中的消化过程的快照图像,这些细胞器负责凋亡细胞尸体的吞噬降解的实际执行。我们将探针用于正常胸腺的组织切片和一些人类淋巴瘤中的吞噬反应的可视化。我们还讨论了DNase II型断裂作为吞噬活性标记的性质,稳定性和特性。这一进展为研究必须清除死亡细胞的病理学(例如癌症,炎症,感染和自身免疫性疾病)提供了有用的荧光工具。

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