Glogauer M, Hartwig J, Stossel T
Hematology Division, Brigham and Women's Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Cell Biol. 2000 Aug 21;150(4):785-96. doi: 10.1083/jcb.150.4.785.
We developed a permeabilization method that retains coupling between N-formyl-methionyl-leucyl-phenylalanine tripeptide (FMLP) receptor stimulation, shape changes, and barbed-end actin nucleation in human neutrophils. Using GTP analogues, phosphoinositides, a phosphoinositide-binding peptide, constitutively active or inactive Rho GTPase mutants, and activating or inhibitory peptides derived from neural Wiskott-Aldrich syndrome family proteins (N-WASP), we identified signaling pathways leading from the FMLP receptor to actin nucleation that require Cdc42, but then diverge. One branch traverses the actin nucleation pathway involving N-WASP and the Arp2/3 complex, whereas the other operates through active Rac to promote actin nucleation. Both pathways depend on phosphoinositide expression. Since maximal inhibition of the Arp2/3 pathway leaves an N17Rac inhibitable alternate pathway intact, we conclude that this alternate involves phosphoinositide-mediated uncapping of actin filament barbed ends.
我们开发了一种通透化方法,该方法可保持人中性粒细胞中N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸三肽(FMLP)受体刺激、形态变化和肌动蛋白丝末端肌动蛋白成核之间的偶联。使用GTP类似物、磷酸肌醇、磷酸肌醇结合肽、组成型激活或失活的Rho GTPase突变体,以及源自神经Wiskott-Aldrich综合征家族蛋白(N-WASP)的激活或抑制肽,我们确定了从FMLP受体到肌动蛋白成核的信号通路,该通路需要Cdc42,但随后会发生分歧。一个分支穿过涉及N-WASP和Arp2/3复合体 的肌动蛋白成核途径,而另一个分支则通过活性Rac起作用以促进肌动蛋白成核。这两条途径均依赖于磷酸肌醇的表达。由于对Arp2/3途径的最大抑制使N17Rac可抑制的替代途径保持完整,我们得出结论,这种替代涉及磷酸肌醇介导的肌动蛋白丝末端的去封闭。