You J, Aznavoorian S, Liotta L A, Dong C
Cellular Biomechanics Laboratory, Bioengineering Program, Pennsylvania State University, University Park 16802, USA.
J Cell Physiol. 1996 Apr;167(1):156-63. doi: 10.1002/(SICI)1097-4652(199604)167:1<156::AID-JCP18>3.0.CO;2-9.
The potential involvement of osmotically generated force in protrusion of tumor cell pseudopods was examined during a micropipette assay. Experiments were performed on single A2058 melanoma cells activated by a micropipette filled with soluble type IV collagen. Previous observations suggested that tumor cell pseudopod protrusion induced by type IV collagen took place in distinct, separable phases: an initial bleb (first phase) caused by localized Ca2+-activated actin filament severing resulting in an osmotic flux followed by an extension with an irregular shape (second phase) which required G protein-mediated actin polymerization (Dong et al., 1994, Microvasc. Res., 47:55-67). Presently we studied cell pseudopod protrusion in response to the changes in chemoattractant osmolality. Reduction of attractant osmolality by 20-25% from its baseline value (297 mmol/ kg) resulted in an increase in pseudopod length by 50% apparent in the initial phase. Increases in attractant osmolality by 25-30% from the baseline value arrested pseudopod protrusion significantly during both initial and later phases. Using a dual-pipette method, such osmotic influence on the cell pseudopod protrusion was shown to be only a local effect in a small region where the cell surface was stimulated by the micropipette. While forces derived from actin polymerization and osmotic pressure have been proposed to cause protrusion in general, our results suggested that osmotically generated force is more apparent in the initial phase of the pseudopod formation.
在微量移液器测定过程中,研究了渗透产生的力在肿瘤细胞伪足突出中的潜在作用。实验是在单个A2058黑色素瘤细胞上进行的,这些细胞由充满可溶性IV型胶原的微量移液器激活。先前的观察表明,IV型胶原诱导的肿瘤细胞伪足突出发生在不同的、可分离的阶段:由局部Ca2+激活的肌动蛋白丝切断引起的初始泡状突起(第一阶段),导致渗透通量,随后是不规则形状的延伸(第二阶段),这需要G蛋白介导的肌动蛋白聚合(Dong等人,1994年,《微血管研究》,47:55-67)。目前,我们研究了细胞伪足突出对趋化剂渗透压变化的反应。将趋化剂渗透压从其基线值(297 mmol/kg)降低20-25%,导致伪足长度在初始阶段增加50%。将趋化剂渗透压从基线值增加25-30%,在初始阶段和后期阶段均显著阻止伪足突出。使用双移液器方法,这种对细胞伪足突出的渗透影响被证明只是在微量移液器刺激细胞表面的小区域中的局部效应。虽然一般认为肌动蛋白聚合和渗透压产生的力会导致突出,但我们的结果表明,渗透产生的力在伪足形成的初始阶段更为明显。