Nasrallah V N, Shirley P S, Myrvik Q, Waite M
J Immunol. 1983 Nov;131(5):2104-6.
Polymorphonuclear phagocytes have been shown to undergo marked alteration in oxidative metabolism during phagocytosis. These alterations, collectively known as the "respiratory burst", include increased glucose oxidation through the hexose monophosphate shunt (1), increased oxygen consumption (1), and increased superoxide (O-2)3 (2) and H2O2 production (3). Similar metabolic events have also been shown to occur in the rabbit alveolar macrophage (AM). There is consistent evidence that the macrophage undergoes increased oxygen consumption (4-6) and hexose monophosphate shunt activity (4-9) upon phagocytosis. There are conflicting data, however, concerning the ability of the macrophage to produce O-2. Some studies suggest that macrophages are incapable of producing measurable amounts of O-2 upon phagocytosis (7, 10-12). Other studies, however, suggest that macrophages are indeed capable of producing substantial amounts of O-2 during phagocytosis (8, 13-15). This study was designed to resolve the discrepancies in the literature concerning O-2 production in macrophages.
多形核吞噬细胞已被证明在吞噬过程中氧化代谢会发生显著改变。这些改变统称为“呼吸爆发”,包括通过磷酸己糖途径增加葡萄糖氧化(1)、增加耗氧量(1)以及增加超氧阴离子(O₂⁻)³生成(2)和过氧化氢生成(3)。类似的代谢事件在兔肺泡巨噬细胞(AM)中也有发生。有一致的证据表明巨噬细胞在吞噬时耗氧量增加(4 - 6)以及磷酸己糖途径活性增强(4 - 9)。然而,关于巨噬细胞产生O₂⁻的能力存在相互矛盾的数据。一些研究表明巨噬细胞在吞噬时无法产生可测量量的O₂⁻(7, 10 - 12)。然而,其他研究表明巨噬细胞在吞噬过程中确实能够产生大量的O₂⁻(8, 13 - 15)。本研究旨在解决文献中关于巨噬细胞产生O₂⁻的差异。