Hunninghake G W, Gallin J I, Fauci A S
Am Rev Respir Dis. 1978 Jan;117(1):15-23. doi: 10.1164/arrd.1978.117.1.15.
The generation of a chemotactic factor by guinea pig alveolar macrophages after phagocytosis of heat-killed Staphylococcus aureus was studied. These studies demonstrated that after phagocytosis, alveolar macrophages secrete a small molecular weight (less than 5,000 daltons) chemotactic factor that preferentially attracts neutrophils. The chemotactic factor can be generated in vivo and in vitro, and its chemotactic activity can be detected both in vitro by a chemotactic assay and in vivo by an increase in the absolute number of neutrophils in bronchoalveolar lavage fluid and in lung tissue histologic specimens. Generation of the chemotactic factor was inhibited by 20 microgram of actinomycin D per ml and by 10 microgram of cycloheximide per ml. The factors were stable after incubation at 56 degrees C for 45 min, but not after incubation at 100 degreeg C for 10 min. These studies show that alveolar macrophages can serve as an initiator of pulmonary inflammatory responses by secreting a potent mediator of neutrophil locomotion.
对豚鼠肺泡巨噬细胞吞噬热杀死的金黄色葡萄球菌后趋化因子的产生进行了研究。这些研究表明,吞噬后,肺泡巨噬细胞分泌一种小分子质量(小于5000道尔顿)的趋化因子,该因子优先吸引中性粒细胞。趋化因子可在体内和体外产生,其趋化活性可通过趋化试验在体外检测,也可通过支气管肺泡灌洗液和肺组织组织学标本中中性粒细胞绝对数量的增加在体内检测。每毫升20微克放线菌素D和每毫升10微克环己酰亚胺可抑制趋化因子的产生。这些因子在56℃孵育45分钟后稳定,但在100℃孵育10分钟后不稳定。这些研究表明,肺泡巨噬细胞可通过分泌一种有效的中性粒细胞运动介质,作为肺部炎症反应的启动者。