Kavet R I, Brain J D
J Appl Physiol Respir Environ Exerc Physiol. 1977 Mar;42(3):432-7. doi: 10.1152/jappl.1977.42.3.432.
We present a method which permits analysis of phagocytic behavior in small samples of macrophages. Both overall phagocytic kinetics and intercellular variability in particle uptake were measured. Macrophages lavaged from Syrian golden hamster lungs were incubated (5 min at 37 degrees C) with 2- to 4-mum plastic particles at 4.6, 6.9, 9.1, and 16.0 X 10(6) part./ml. Harvested macrophages ranged from 0.6 to 4.0 X 10(6) cells per animal. To concentrate the cells and separate them from cell-free substrate after termination of phagocytosis, 30-60% of each flask's contents were centrifuged (400 X g, 20 min) atop a Metrizamide subphase (34% wt/vol, rho = 1.18). Cells were collected from the interface, fixed, and visually scored for number of particles phagocytized. Phagocytic rates followed Michaelis-Menten kinetics with Vmax = 0.63 +/- 0.18 (SEM) part./viable cell per min and Km = 8.5 +/- 2.7 (SEM) X 10(6) part./ml. In every case (23/23 flasks from 6 animals) particle uptake exhibited greater (P less than 0.01) cell-to-cell variability in avidity for substrate than the Poisson distribution would predict from mean number of particles phagocytized per viable cell.
我们提出了一种方法,该方法允许对小样本巨噬细胞的吞噬行为进行分析。测量了总体吞噬动力学和颗粒摄取的细胞间变异性。从叙利亚金黄地鼠肺中冲洗出的巨噬细胞在37℃下与2至4μm的塑料颗粒以4.6、6.9、9.1和16.0×10⁶个颗粒/毫升的浓度孵育(5分钟)。每只动物收获的巨噬细胞数量为0.6至4.0×10⁶个细胞。为了在吞噬作用终止后浓缩细胞并将它们与无细胞底物分离,将每个培养瓶内容物的30 - 60%在Metrizamide亚相(34%重量/体积,ρ = 1.18)上离心(400×g,20分钟)。从界面收集细胞,固定,并通过视觉对吞噬的颗粒数量进行评分。吞噬速率遵循米氏动力学,Vmax = 0.63±0.18(标准误)个颗粒/每分钟活细胞,Km = 8.5±2.7(标准误)×10⁶个颗粒/毫升。在每种情况下(来自6只动物的23/23个培养瓶),与泊松分布根据每个活细胞吞噬颗粒的平均数所预测的相比,颗粒摄取在对底物的亲和力方面表现出更大的(P < 0.01)细胞间变异性。