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首页> 外文期刊>eLife journal >Fringe proteins modulate Notch-ligand cis and trans interactions to specify signaling states
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Fringe proteins modulate Notch-ligand cis and trans interactions to specify signaling states

机译:边缘蛋白调节Notch-配体顺式和反式相互作用以指定信号传导状态

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In animals, cells use a process called Notch signaling to communicate with neighboring cells. During this process, a protein known as a DSL ligand from one cell binds to a protein called a Notch receptor on a neighboring cell. This triggers a series of events in the neighboring cell that change how the genes in this cell are expressed. Notch signaling is involved in many processes including the early growth of embryos, the formation of organs and limbs, and the maintenance of stem cells throughout adult life. Enzymes called Fringe enzymes can control Notch signaling by blocking or promoting the formation of the DSL ligand-Notch receptor pairs. It is also possible for a DSL ligand and a Notch receptor from the same cell to interact. This is thought to be important because it prevents an individual cell from sending and receiving Notch signals at the same time. There are several different DSL ligands, Notch receptors and Fringe enzymes, so it is difficult to determine which configurations of receptors, ligands and Fringe enzymes can enable Notch signals to be sent or received. To address this problem, LeBon et al. investigated how Fringe enzymes acted on several different DSL-Notch receptor pairs in mammalian cells, and also in fruit flies. They focused in particular on the interactions that occurred within the same cell, as the role of Fringe enzymes in this type of interaction has not been examined previously. The experiments revealed that Fringe proteins modify specific same-cell interactions in a way that enables a cell to receive one type of Notch signal from a neighboring cell and send a different type of Notch signal to another cell at the same time. More generally, these results show how an unconventional, ‘bottom-up’ approach can reveal the design principles of cell signaling systems, and suggest that it should now be possible to use these principles to try to understand which cell types send signals to which other cell types in many different contexts.
机译:在动物中,细胞使用称为Notch信号的过程与邻近细胞通信。在此过程中,来自一个细胞的称为DSL配体的蛋白质与相邻细胞上称为Notch受体的蛋白质结合。这触发了邻近细胞中的一系列事件,这些事件改变了该细胞中基因的表达方式。 Notch信号传导参与许多过程,包括胚胎的早期生长,器官和四肢的形成以及整个成年后维持干细胞。称为边缘酶的酶可以通过阻断或促进DSL配体-Notch受体对的形成来控制Notch信号传导。来自同一细胞的DSL配体和Notch受体也可能相互作用。人们认为这很重要,因为它阻止了单个小区同时发送和接收Notch信号。存在几种不同的DSL配体,Notch受体和Fringe酶,因此很难确定受体,配体和Fringe酶的哪些配置可以使Notch信号得以发送或接收。为了解决这个问题,LeBon等人。研究了Fringe酶如何作用于哺乳动物细胞以及果蝇中的几种不同的DSL-Notch受体对。他们特别关注于同一细胞内发生的相互作用,因为之前尚未研究边缘酶在此类相互作用中的作用。实验表明,边缘蛋白以一种使细胞能够从邻近细胞接收一种类型的Notch信号并同时向另一种细胞发送不同类型的Notch信号的方式修饰特定的同细胞相互作用。更概括地说,这些结果表明了一种非常规的“自下而上”的方法如何揭示细胞信号系统的设计原理,并建议现在应该可以使用这些原理来尝试了解哪些细胞类型向其他细胞发送信号。在许多不同情况下的细胞类型。

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