Merlot Sylvain, Firtel Richard A
Section of Cell and Developmental Biology, Division of Biological Sciences and Center for Molecular Genetics, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0634, USA.
J Cell Sci. 2003 Sep 1;116(Pt 17):3471-8. doi: 10.1242/jcs.00703.
Chemoattractant-responsive cells are able to translate a shallow extracellular chemical gradient into a steep intracellular gradient resulting in the localization of F-actin assembly at the front and an actomyosin network at the rear that moves the cell forward. Recent evidence suggests that one of the first asymmetric cellular responses is the localized accumulation of PtdIns(3,4,5)P3, the product of class I phosphoinositide 3-kinase (PI3K) at the site of the new leading edge. The strong accumulation of PtdIns(3,4,5)P3 results from the localized activation of PI3K and also from feedback loops that amplify PtdIns(3,4,5)P3 synthesis at the front and control its degradation at the side and back of cells. These different pathways are temporally and spatially regulated and integrate with other signaling pathways during directional sensing and chemotaxis.
化学引诱剂反应性细胞能够将浅的细胞外化学梯度转化为陡峭的细胞内梯度,导致F-肌动蛋白组装在前部定位,肌动球蛋白网络在后部定位,从而使细胞向前移动。最近的证据表明,最早的不对称细胞反应之一是I类磷脂酰肌醇3-激酶(PI3K)的产物PtdIns(3,4,5)P3在新前沿部位的局部积累。PtdIns(3,4,5)P3的强烈积累源于PI3K的局部激活,也源于反馈回路,这些回路在前部放大PtdIns(3,4,5)P3的合成,并在细胞侧面和后部控制其降解。这些不同的途径在时间和空间上受到调节,并在方向感知和趋化作用期间与其他信号通路整合。