Worth Randall G, Kim Moo-Kyung, Kindzelskii Andrei L, Petty Howard R, Schreiber Alan D
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4533-8. doi: 10.1073/pnas.0836650100. Epub 2003 Apr 3.
Calcium oscillations and traveling calcium waves have been observed in living cells, although amino acid sequences regulating wave directionality and downstream cell functions have not been reported. In this study we identify an amino acid sequence within the cytoplasmic domain of the leukocyte IgG receptor Fc gamma RIIA that affects the amplitude of calcium spikes and the spatiotemporal dynamics of calcium waves in the vicinity of phagosomes. By using high-speed microscopy to map calcium-signaling routes within cells, we have discovered that bound IgG-coated targets trigger two calcium waves traveling in opposite directions about the perimeter of cells expressing Fc gamma RIIA. After phagocytosis, one calcium wave propagates around the plasma membrane to the site of phagocytosis where it splits into two calcium signals: one traveling to and encircling the phagosome once, and the second continuing around the plasma membrane to the point of origin. However, in a genetically engineered form of Fc gamma RIIA containing a mutation in the cytoplasmic L-T-L motif, the calcium signal travels around the plasma membrane, but is not properly routed to the phagosome. Furthermore, these calcium pattern-deficient mutants were unable to support phagolysosome fusion, although recruitment of phagolysosome-associated proteins lysosome-associated protein 1, Rab5, and Rab7 were normal. Our findings suggest that: (i) calcium signaling is a late step in phagolysosome fusion, (ii) a line of communication exists between the plasma membrane and phagosome, and (iii) the L-T-L motif is a signal sequence for calcium signal routing to the phagosome.
在活细胞中已观察到钙振荡和钙行波,尽管尚未报道调节波方向性和下游细胞功能的氨基酸序列。在本研究中,我们鉴定出白细胞IgG受体FcγRIIA胞质结构域内的一个氨基酸序列,该序列影响钙尖峰的幅度以及吞噬体附近钙波的时空动态。通过使用高速显微镜绘制细胞内的钙信号传导途径,我们发现结合有IgG的包被靶标会触发两个沿表达FcγRIIA的细胞周边向相反方向传播的钙波。吞噬作用后,一个钙波围绕质膜传播到吞噬作用位点,在那里它分裂为两个钙信号:一个传播到吞噬体并环绕其一圈,另一个继续围绕质膜回到起点。然而,在细胞质L-T-L基序中含有突变的基因工程形式的FcγRIIA中,钙信号围绕质膜传播,但没有正确地传导至吞噬体。此外,这些钙信号模式缺陷的突变体无法支持吞噬溶酶体融合,尽管吞噬溶酶体相关蛋白溶酶体相关膜蛋白1、Rab5和Rab7的募集是正常的。我们的研究结果表明:(i)钙信号传导是吞噬溶酶体融合的后期步骤,(ii)质膜和吞噬体之间存在一条通讯线路,(iii)L-T-L基序是钙信号传导至吞噬体的信号序列。