Kasahara Kousuke, Nakayama Yuji, Kihara Akio, Matsuda Daisuke, Ikeda Kikuko, Kuga Takahisa, Fukumoto Yasunori, Igarashi Yasuyuki, Yamaguchi Naoto
Department of Molecular Cell Biology, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba 260-8675, Japan.
Exp Cell Res. 2007 Jul 15;313(12):2651-66. doi: 10.1016/j.yexcr.2007.05.001. Epub 2007 May 8.
Src-family kinases (SFKs) are co-expressed with multiple combinations of each member in a single cell and involved in various signalings. Recently, we showed by sucrose-density gradient fractionation that the subcellular distribution of c-Src is distinct from that of Lyn. However, little is known about the trafficking of c-Src in living cells. Here, we show by time-lapse monitoring combined with photobleaching techniques that c-Src, a non-palmitoylated SFK, is rapidly exchanged between the plasma membrane and intracellular organelles representing late endosomes/lysosomes possibly through its cytosolic release. Although Lyn, a palmitoylated SFK, is exocytosed to the plasma membrane via the Golgi apparatus along the secretory pathway, lack of palmitoylation directs Lyn away from the exocytotic transport to the c-Src-type trafficking between the plasma membrane and late endosomes/lysosomes. Intriguingly, c-Src and a non-palmitoylated Lyn mutant are efficiently delivered and immobilized to focal adhesions when their SH2 domains are able to mediate protein-protein interactions in place of intramolecular bindings. However, palmitoylation of Lyn inhibits its recruitment to focal adhesions. These results suggest that palmitoylation of SFKs is critical for SFK localization and trafficking and implicate that two distinct trafficking pathways for SFKs may be involved in SFKs' specific functions.
Src家族激酶(SFKs)在单个细胞中与每个成员的多种组合共同表达,并参与各种信号传导。最近,我们通过蔗糖密度梯度分级分离法表明,c-Src的亚细胞分布与Lyn不同。然而,关于c-Src在活细胞中的运输情况知之甚少。在这里,我们通过延时监测结合光漂白技术表明,c-Src是一种非棕榈酰化的SFK,可能通过其胞质释放,在质膜和代表晚期内体/溶酶体的细胞内细胞器之间快速交换。虽然棕榈酰化的SFK——Lyn沿着分泌途径通过高尔基体被胞吐到质膜,但缺乏棕榈酰化会使Lyn偏离胞吐运输,转向质膜与晚期内体/溶酶体之间的c-Src型运输。有趣的是,当c-Src和非棕榈酰化的Lyn突变体的SH2结构域能够介导蛋白质-蛋白质相互作用以取代分子内结合时,它们能有效地被递送至粘着斑并固定在那里。然而,Lyn的棕榈酰化会抑制其向粘着斑的募集。这些结果表明,SFKs的棕榈酰化对于SFK的定位和运输至关重要,并且暗示SFKs的两种不同运输途径可能参与了SFKs的特定功能。