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对盘基网柄菌细胞进行均匀的环磷酸腺苷刺激会诱导信号转导和伪足的局部斑块形成。

Uniform cAMP stimulation of Dictyostelium cells induces localized patches of signal transduction and pseudopodia.

作者信息

Postma Marten, Roelofs Jeroen, Goedhart Joachim, Gadella Theodorus W J, Visser Antonie J W G, Van Haastert Peter J M

机构信息

Department of Biochemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, the Netherlands.

出版信息

Mol Biol Cell. 2003 Dec;14(12):5019-27. doi: 10.1091/mbc.e03-08-0566. Epub 2003 Oct 31.

Abstract

The chemoattractant cAMP induces the translocation of cytosolic PHCrac-GFP to the plasma membrane. PHCrac-GFP is a green fluorescent protein fused to a PH domain that presumably binds to phosphatydylinositol polyphosphates in the membrane. We determined the relative concentration of PHCrac-GFP in the cytosol and at different places along the cell boundary. In cells stimulated homogeneously with 1microM cAMP we observed two distinct phases of PHCrac-GFP translocation. The first translocation is transient and occurs to nearly the entire boundary of the cell; the response is maximal at 6-8 s after stimulation and disappears after approximately 20 s. A second translocation of PHCrac-GFP starts after approximately 30 s and persists as long as cAMP remains present. Translocation during this second response occurs to small patches with radius of approximately 4-5 microm, each covering approximately 10% of the cell surface. Membrane patches of PHCrac-GFP are both temporally and spatially closely associated with pseudopodia, which are extended at approximately 10 s from the area with a PHCrac-GFP patch. These signaling patches in pseudopodia of homogeneously stimulated cells resemble the single patch of PHCrac-GFP at the leading edge of a cell in a gradient of cAMP, suggesting that PHCrac-GFP is a spatial cue for pseudopod formation also in uniform cAMP.

摘要

趋化因子cAMP可诱导胞质PHCrac-GFP转位至质膜。PHCrac-GFP是一种绿色荧光蛋白,与一个PH结构域融合,该结构域可能与膜中的磷脂酰肌醇多磷酸结合。我们测定了胞质中以及细胞边界不同位置处PHCrac-GFP的相对浓度。在用1微摩尔/升cAMP均匀刺激的细胞中,我们观察到PHCrac-GFP转位有两个不同阶段。第一次转位是短暂的,几乎发生在细胞的整个边界;刺激后6 - 8秒时反应最大,约20秒后消失。PHCrac-GFP的第二次转位在大约30秒后开始,只要cAMP存在就会持续。第二次反应期间的转位发生在半径约为4 - 5微米的小斑块处,每个斑块覆盖细胞表面的约10%。PHCrac-GFP的膜斑块在时间和空间上都与伪足紧密相关,伪足在大约10秒时从有PHCrac-GFP斑块的区域伸出。均匀刺激细胞伪足中的这些信号斑块类似于在cAMP梯度中细胞前沿的单个PHCrac-GFP斑块,这表明PHCrac-GFP在均匀cAMP中也是伪足形成的空间线索。

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