Motosugi H, Graham L, Noblitt T W, Doyle N A, Quinlan W M, Li Y, Doerschuk C M
Herman B. Wells Center for Pediatric Research, Indiana University Medical Center, Indianapolis, USA.
Am J Pathol. 1996 Sep;149(3):963-73.
Complement fragment-induced sequestration of neutrophils within the lungs may be mediated by stimulus-induced decreases in the deformability of neutrophils, prolonging their lung capillary transit times. As changes in deformability often occur through changes in cytoskeletal proteins, this study determined whether the distribution of actin within intracapillary neutrophils was altered by intravascular complement fragments and whether sequestered neutrophils were less deformed. Ultrathin cryosections of lung tissue from rabbits given an infusion of complement fragments or saline were immunolabeled with anti-actin antibodies. The number of gold particles/microvillus and the density of gold particles/microgram 2 cytoplasm in the submembrane and the central region of intracapillary neutrophils was quantitated. Neutrophil shape was evaluated using laser confocal microscopy. In control rabbits, the ratio of submembrane/central gold was always greater than one and most neutrophils were elongated, 97% having shape factors > 1.10. The ratio of submembrane/central gold was greater in complement-treated rabbits (5.1 +/- 0.9) than controls (2.6 +/- 0.4; P < 0.026). The number of gold particles/microvillus was also increased in complement-treated rabbits (3.9 +/- 0.5) compared with controls (2.3 +/- 0.5; P < 0.045). Neutrophils were more often spherical when rabbits received complement fragments for 1.5 minutes than in control lungs or after 15-minute infusions. These data suggest that complement fragments induce a rapid redistribution of actin from the central to the submembrane region and the microvilli and result in more round neutrophils. This redistribution may decrease the deformability of neutrophils by altering the stiffness of the submembrane region and/or by preventing the microvilli from flattening.
补体片段诱导的中性粒细胞在肺内滞留可能是由刺激导致中性粒细胞变形能力下降介导的,这延长了它们在肺毛细血管中的转运时间。由于变形能力的变化通常通过细胞骨架蛋白的变化而发生,本研究确定血管内补体片段是否会改变毛细血管内中性粒细胞中肌动蛋白的分布,以及滞留的中性粒细胞是否变形性更小。给输注补体片段或生理盐水的兔子的肺组织制作超薄冰冻切片,并用抗肌动蛋白抗体进行免疫标记。对毛细血管内中性粒细胞的亚膜和中央区域每微绒毛的金颗粒数量以及每微克²细胞质的金颗粒密度进行定量。使用激光共聚焦显微镜评估中性粒细胞的形状。在对照兔子中,亚膜/中央金的比例总是大于1,大多数中性粒细胞呈细长形,97%的形状因子>1.10。补体处理的兔子中,亚膜/中央金的比例(5.1±0.9)高于对照组(2.6±0.4;P<0.026)。与对照组(2.3±0.5;P<0.045)相比,补体处理的兔子中每微绒毛的金颗粒数量也增加了(3.9±0.5)。与对照肺或输注15分钟后相比,兔子接受补体片段1.5分钟时中性粒细胞更常呈球形。这些数据表明,补体片段诱导肌动蛋白从中央区域快速重新分布到亚膜区域和微绒毛,导致中性粒细胞更圆。这种重新分布可能通过改变亚膜区域的硬度和/或阻止微绒毛变平来降低中性粒细胞的变形能力。