Skalak R, Skierczynski B A, Wung S L, Chien S, Usami S
Institute of Biomedical Engineering, University of California-San Diego, La Jolla 92093-0412.
Blood Cells. 1993;19(2):389-97; discussion 398-9.
The active locomotion of polymorphonuclear leukocytes into a glass pipette has been recently reported using formyl-methionyl-leucyl-phenylalanine (fMLP) as a chemoattractant. The frontal portion of the leukocyte appears clear and free of granules as observed in pseudopod formation. Three possible mechanisms for pseudopod formation are considered: (1) pressure-flow generated by actin-myosin contraction at the rear of the cell or at the base of the pseudopod; (2) osmotic pressure generated at the cell membrane, interior to the cell; and (3) actin polymerization of the cell membrane at the leading edge of the pseudopod. Experimental data on the movement of F-actin toward the rear of the cell, away from the front, favors polymerization of G-actin to F-actin at the leading edge. The active role of osmotic pressure and contraction at the base of the pseudopod are possible but not yet proven.
最近有报道称,使用甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)作为趋化剂,多形核白细胞可主动移动到玻璃移液管中。如在伪足形成过程中所观察到的,白细胞的前部看起来清晰且无颗粒。人们考虑了伪足形成的三种可能机制:(1)细胞后部或伪足基部由肌动蛋白-肌球蛋白收缩产生的压力流;(2)细胞内部细胞膜处产生的渗透压;(3)伪足前缘细胞膜的肌动蛋白聚合。关于F-肌动蛋白朝细胞后部移动、远离前部的实验数据,支持G-肌动蛋白在前缘聚合成F-肌动蛋白。渗透压和伪足基部收缩的积极作用是可能的,但尚未得到证实。