F- and G-Actin Concentrations in Lamellipodia of Moving Cells

被引:96
作者
Koestler, Stefan A. [1 ]
Rottner, Klemens [2 ]
Lai, Frank [2 ]
Block, Jennifer [2 ]
Vinzenz, Marlene [1 ]
Small, Victor [1 ]
机构
[1] Austrian Acad Sci, Inst Mol Biotechnol, A-1010 Vienna, Austria
[2] Helmholtz Ctr Infect Res HZI, Cytoskeleton Dynam Grp, Braunschweig, Germany
来源
PLOS ONE | 2009年 / 4卷 / 03期
关键词
D O I
10.1371/journal.pone.0004810
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cells protrude by polymerizing monomeric (G) into polymeric (F) actin at the tip of the lamellipodium. Actin filaments are depolymerized towards the rear of the lamellipodium in a treadmilling process, thereby supplementing a G-actin pool for a new round of polymerization. In this scenario the concentrations of F- and G-actin are principal parameters, but have hitherto not been directly determined. By comparing fluorescence intensities of bleached and unbleached regions of lamellipodia in B16-F1 mouse melanoma cells expressing EGFP-actin, before and after extraction with Triton X-100, we show that the ratio of F- to G-actin is 3.2+/-0.9. Using electron microscopy to determine the F- actin content, this ratio translates into F- and G-actin concentrations in lamellipodia of approximately 500 mu M and 150 mu M, respectively. The excess of G-actin, at several orders of magnitude above the critical concentrations at filament ends indicates that the polymerization rate is not limited by diffusion and is tightly controlled by polymerization/ depolymerization modulators.
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页数:5
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