Vujicic Snezana, Feng Lanfei, Antoni Angelika, Rauch Joyce, Levine Jerrold S
Section of Nephrology, Department of Medicine, University of Illinois at Chicago; Section of Nephrology, Department of Medicine, Jesse Brown Veterans Affairs Medical Center.
Department of Biology, Kutztown University of Pennsylvania.
J Vis Exp. 2016 Dec 27(118):54980. doi: 10.3791/54980.
Cells dying by apoptosis, also referred to as regulated cell death, acquire multiple new activities that enable them to influence the function of adjacent live cells. Vital activities, such as survival, proliferation, growth, and differentiation, are among the many cellular functions modulated by apoptotic cells. The ability to recognize and respond to apoptotic cells appears to be a universal feature of all cells, regardless of lineage or organ of origination. However, the diversity and complexity of the response to apoptotic cells mandates that great care be taken in dissecting the signaling events and pathways responsible for any particular outcome. In particular, one must distinguish among the multiple mechanisms by which apoptotic cells can influence intracellular signaling pathways within viable responder cells, including: receptor-mediated recognition of the apoptotic cell, release of soluble mediators by the apoptotic cell, and/or engagement of the phagocytic machinery. Here, we provide a protocol for identifying intracellular signaling events that are induced in viable responder cells following their exposure to apoptotic cells. A major advantage of the protocol lies in the attention it pays to dissection of the mechanism by which apoptotic cells modulate signaling events within responding cells. While the protocol is specific for a conditionally immortalized mouse kidney proximal tubular cell line (BU.MPT cells), it is easily adapted to cell lines that are non-epithelial in origin and/or derived from organs other than the kidney. The use of dead cells as a stimulus introduces several unique factors that can hinder the detection of intracellular signaling events. These problems, as well as strategies to minimize or circumvent them, are discussed within the protocol. Application of this protocol should aid our expanding knowledge of the broad influence that dead or dying cells exert on their live neighbors, both in health and in disease.
通过凋亡死亡的细胞,也被称为程序性细胞死亡,会获得多种新活性,使其能够影响相邻活细胞的功能。诸如存活、增殖、生长和分化等重要活动,是凋亡细胞调节的众多细胞功能之一。识别和响应凋亡细胞的能力似乎是所有细胞的普遍特征,无论其起源的谱系或器官如何。然而,对凋亡细胞的反应具有多样性和复杂性,这就要求在剖析导致任何特定结果的信号事件和途径时要格外小心。特别是,必须区分凋亡细胞影响存活反应细胞内信号通路的多种机制,包括:受体介导的对凋亡细胞的识别、凋亡细胞释放可溶性介质,和/或吞噬机制的参与。在这里,我们提供了一个方案,用于识别存活的反应细胞在接触凋亡细胞后诱导的细胞内信号事件。该方案的一个主要优点在于它关注剖析凋亡细胞调节反应细胞内信号事件的机制。虽然该方案特定适用于条件永生化的小鼠肾近端小管细胞系(BU.MPT细胞),但它很容易适用于非上皮起源和/或源自肾脏以外器官的细胞系。使用死细胞作为刺激物会引入几个独特的因素,这些因素可能会阻碍细胞内信号事件的检测。这些问题以及将其最小化或规避的策略将在方案中进行讨论。应用该方案应有助于我们进一步了解死亡或濒死细胞在健康和疾病状态下对其活邻居产生的广泛影响。