首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Changes in neutrophil actin and shape during sequestration induced by complement fragments in rabbits.
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Changes in neutrophil actin and shape during sequestration induced by complement fragments in rabbits.

机译:补体碎片诱导的螯合过程中中性粒细胞肌动蛋白和形状的变化。

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摘要

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.
机译:补体片段诱导的肺中性粒细胞螯合可以通过刺激诱导的嗜中性粒细胞可变形性降低而介导,从而延长它们的肺毛细血管通过时间。由于可变形性的变化通常是通过细胞骨架蛋白的变化而发生的,因此本研究确定了血管内补体片段是否改变了肌动蛋白在毛细血管内嗜中性粒细胞中的分布,以及螯合的嗜中性粒细胞是否变形较小。输注补体片段或盐水的兔肺组织超薄冰冻切片用抗肌动蛋白抗体进行免疫标记。定量分析毛细血管内嗜中性粒细胞的亚膜和中央区域的金颗粒/微绒毛数目和金颗粒/微克2细胞质的密度。使用激光共聚焦显微镜评估中性粒细胞的形状。在对照兔中,亚膜/中央金之比始终大于1,大多数中性粒细胞被拉长,其中97%的形状因子> 1.10。补体治疗的兔子(5.1 +/- 0.9)中的亚膜/中央金之比大于对照组(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(3.9 +/- 0.5)中的金颗粒/微绒毛数目也增加了。当兔子接受补体片段1.5分钟时,中性粒细胞比对照组肺中或输注15分钟后更呈球形。这些数据表明补体片段诱导肌动蛋白从中央快速转移到膜下区域和微绒毛,并导致更圆形的中性粒细胞。这种重新分布可通过改变亚膜区域的硬度和/或通过防止微绒毛变平而降低中性粒细胞的可变形性。

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