Rodionov S V, Zemskov V M, Glushkov M V
Tsitologiia. 1996;38(9):983-90.
It is known that functional activity of macrophages (Mph), adhesion and phagocytosis, depends on the local concentration of Fc receptors (Fc gamma R) on the cell surface. Fc gamma R may have a random distribution on cell membrane or form clusters of different sizes. This process depends on the local activity of microfilaments that, in its turn, reflects peculiarities of macrophage microenvironments. One may conceive that the number of opsonized erythrocytes (OE) subject to adhesion (engulfing) to separate Mph depends on the amount of active centres on the cell surface and their activity. The structures, such as Fc gamma R clusters, phagosomes and others, in whose formation numerous components of Mph (cell skeleton, microvesicles, signal receptive system and others) are involved, are arbitrarily called the structural functional units (SFU). Thus, we used two parameters: the average number of SFU per Mph in population, and the average activity of SFU instead of a generally accepted number of OE per Mph. The number of SFU per Mph can be 0, 1, 2 etc., and one SFU may bind (engulf) 0, 1, 2 etc. EA. For the assessment of the parameters, the approximation of experimental histograms by type-A Neyman's distribution was used. To verify the adequacy of the model, observations of OE adhesion and phagocytosis in different conditions were made. The results show that the parameters of the model fit well the biological processes in this system.
众所周知,巨噬细胞(Mph)的功能活性,即黏附与吞噬作用,取决于细胞表面Fc受体(FcγR)的局部浓度。FcγR可能在细胞膜上呈随机分布,或形成不同大小的簇。这个过程取决于微丝的局部活性,而微丝的局部活性又反映了巨噬细胞微环境的特点。可以设想,与单个巨噬细胞发生黏附(吞噬)的调理红细胞(OE)的数量,取决于细胞表面活性中心的数量及其活性。诸如FcγR簇、吞噬体等结构,其形成涉及巨噬细胞的众多成分(细胞骨架、微泡、信号接收系统等),被随意称为结构功能单位(SFU)。因此,我们使用了两个参数:群体中每个巨噬细胞的SFU平均数量,以及SFU的平均活性,而非普遍接受的每个巨噬细胞的OE数量。每个巨噬细胞的SFU数量可以是0、1、2等,且一个SFU可以结合(吞噬)0、1、2等个EA。为评估这些参数,使用了A型奈曼分布对实验直方图进行近似。为验证模型的适用性,对不同条件下OE的黏附与吞噬进行了观察。结果表明,该模型的参数与该系统中的生物学过程拟合良好。