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[摘要]：Rac1 and Rac2, which belong to the Rho subfamily of Ras-related GTPascs, play an essential role in activation of gp91(phox)/Nox2 (cytochrome b-245, beta polypeptide; also known as Cybb), the catalytic core of the superoxide-producing NADPH oxidase in phagocytes. Rac1 also contributes to activation of the non-phagocytic oxidases, Nox1 (NADPH oxidase 1) and Nox3 (NADPH oxidase 3), each related closely to gp91(phox)/Nox2. It has remained controversial whether the insert region of Rac (amino acids 123-135), unique to the Rho subfamily proteins, is involved in gp91(phox)/Nox2 activation. In the present study we show that removal of the insert region from Rac I neither affects activation of gp91(phox)/Nox2, which is reconstituted under cell-free and whole-cell conditions, nor blocks its localization to phagosomes C, during ingestion of IgG-coated beads by macrophage-like RAW264.7 cells. The insert region of Rac2 is also dispensable for gp91(phox)/Nox2 activation at the cellular level. Although Rac2, as well as Rac I, is capable of enhancing Superoxide production by Nox1 and Nox3, the enhancements by the two GTPases are both independent of the insert region. We also demonstrate that Rac3, a third member of the Rac family in mammals, has an ability to activate the three oxidases and that the activation does not require the insert region. Thus the insert region of the Rac GTPases does not participate in regulation of the Nox family NADPH oxidases. |
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