Britigan B E, Coffman T J, Adelberg D R, Cohen M S
Department of Internal Medicine, Veterans Administration Medical Center, Iowa City, Iowa.
J Exp Med. 1988 Dec 1;168(6):2367-72. doi: 10.1084/jem.168.6.2367.
Monocytes lack lactoferrin and have much less myeloperoxidase than neutrophils. They also acquire a potential catalyst for .OH production (tartrate-resistant acid phosphatase) as they differentiate into macrophages. Consequently, the nature of free radicals produced by these cells was examined using the previously developed spin-trapping system. When stimulated with either PMA or OZ neither monocytes nor monocyte-derived macrophages (MDM) exhibited spin trap evidence of .OH formation. Pretreatment with IFN-gamma failed to induce MDM .OH production. When provided with an exogenous Fe+3 catalyst, both stimulated monocytes and MDM, but not PMN, exhibited sustained .OH production, presumably due to the absence of lactoferrin in mononuclear phagocytes. Sustained production of .OH could contribute to the microbicidal activity of mononuclear phagocytes as well as inflammatory tissue damage under in vivo conditions where catalytic Fe+3 may be present.
单核细胞缺乏乳铁蛋白,其髓过氧化物酶比中性粒细胞少得多。当它们分化为巨噬细胞时,还会获得一种产生·OH的潜在催化剂(抗酒石酸酸性磷酸酶)。因此,使用先前开发的自旋捕获系统研究了这些细胞产生的自由基的性质。当用佛波酯(PMA)或臭氧(OZ)刺激时,单核细胞和单核细胞衍生的巨噬细胞(MDM)均未表现出自旋捕获证据表明有·OH形成。用γ干扰素预处理未能诱导MDM产生·OH。当提供外源性Fe+3催化剂时,受刺激的单核细胞和MDM(但不是PMN)均表现出持续的·OH产生,这可能是由于单核吞噬细胞中缺乏乳铁蛋白。在体内可能存在催化性Fe+3的条件下,持续产生·OH可能有助于单核吞噬细胞的杀菌活性以及炎症组织损伤。