Heyworth P G, Knaus U G, Settleman J, Curnutte J T, Bokoch G M
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California 92037.
Mol Biol Cell. 1993 Nov;4(11):1217-23. doi: 10.1091/mbc.4.11.1217.
Activation of the NADPH oxidase of phagocytic cells requires the action of Rac2 or Rac1, members of the Ras superfamily of GTP-binding proteins. Rac proteins are active when in the GTP-bound form and can be regulated by a variety of proteins that modulate the exchange of GDP for GTP and/or GTP hydrolysis. The p190 Rac GTPase Activating Protein (GAP) inhibits human neutrophil NADPH oxidase activity in a cell-free assay system with a K1 of approximately 100 nM. Inhibition by p190 was prevented by GTP gamma S, a nonhydrolyzable analogue of GTP. Similar inhibition was seen with a second protein exhibiting Rac GAP activity, CDC42Hs GAP. The effect of p190 on superoxide (O2-) formation was reversed by the addition of a constitutively GTP-bound Rac2 mutant or Rac1-GTP gamma S but not by RhoA-GTP gamma S. Addition of p190 to an activated oxidase produced no inhibitory effect, suggesting either that p190 no longer has access to Rac in the assembled oxidase or that Rac-GTP is not required for activity once O2- generation has been initiated. These data confirm the role of Rac in NADPH oxidase regulation and support the view that it is the GTP form of Rac that is necessary for oxidase activation. Finally, they raise the possibility that NADPH oxidase may be regulated by the action of GAPs for Rac proteins.
吞噬细胞的NADPH氧化酶的激活需要Rac2或Rac1的作用,它们是GTP结合蛋白的Ras超家族成员。Rac蛋白在结合GTP时呈活性状态,并且可以被多种调节GDP与GTP交换和/或GTP水解的蛋白质所调控。在无细胞分析系统中,p190 Rac GTP酶激活蛋白(GAP)以约100 nM的K1抑制人中性粒细胞NADPH氧化酶活性。GTPγS(一种不可水解的GTP类似物)可阻止p190的抑制作用。另一种具有Rac GAP活性的蛋白CDC42Hs GAP也观察到类似的抑制作用。添加组成型结合GTP的Rac2突变体或Rac1-GTPγS可逆转p190对超氧化物(O2-)形成的影响,但添加RhoA-GTPγS则不能。将p190添加到活化的氧化酶中没有产生抑制作用,这表明要么p190在组装好的氧化酶中无法再接触到Rac,要么一旦O2-生成开始,Rac-GTP对于活性就不再是必需的。这些数据证实了Rac在NADPH氧化酶调节中的作用,并支持了这样一种观点,即Rac的GTP形式对于氧化酶激活是必需的。最后,它们提出了NADPH氧化酶可能受Rac蛋白的GAP作用调节的可能性。