PtdIns(3,4,5)P3 binding is necessary for WAVE2-induced formation of lamellipodia

被引:0
|
作者
Tsukasa Oikawa
Hideki Yamaguchi
Toshiki Itoh
Masayoshi Kato
Takeshi Ijuin
Daisuke Yamazaki
Shiro Suetsugu
Tadaomi Takenawa
机构
[1] Institute of Medical Science,Department of Biochemistry
[2] University of Tokyo,Division of Cancer Genomics
[3] 4-6-1 Shirokanedai,undefined
[4] Minato-ku,undefined
[5] Institute of Medical Science,undefined
[6] University of Tokyo,undefined
[7] 4-6-1 Shirokanedai,undefined
[8] Minato-ku,undefined
[9] CREST,undefined
[10] Japan Science and Technology Corporation (JST),undefined
[11] Minato-ku,undefined
来源
Nature Cell Biology | 2004年 / 6卷
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摘要
Polarized cell movement is triggered by the development of a PtdIns(3,4,5)P3 gradient at the membrane, which is followed by rearrangement of the actin cytoskeleton. The WASP family verprolin homologous protein (WAVE) is essential for lamellipodium formation at the leading edge by activating the Arp2/3 complex downstream of Rac GTPase. Here, we report that WAVE2 binds to PtdIns(3,4,5)P3 through its basic domain. The amino-terminal portion of WAVE2, which includes the PtdIns(3,4,5)P3-binding sequence, was localized at the leading edge of lamellipodia induced by an active form of Rac (RacDA) or by treatment with platelet-derived growth factor (PDGF). Production of PtdIns(3,4,5)P3 at the cell membrane by myristoylated phosphatidylinositol-3-OH kinase (PI(3)K) is sufficient to recruit WAVE2 in the presence of dominant-negative Rac and latrunculin, demonstrating that PtdIns(3,4,5)P3 alone is able to recruit WAVE2. Expression of a full-length mutant of WAVE2 that lacks the lipid-binding activity inhibited proper formation of lamellipodia induced by RacDA. These results suggest that one of the products of PI(3)K, PtdIns(3,4,5)P3, recruits WAVE2 to the polarized membrane and that this recruitment is essential for lamellipodium formation at the leading edge.
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页码:420 / 426
页数:6
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