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本文引用的文献

1
Big roles for small GTPases in the control of directed cell movement.小GTP酶在定向细胞运动控制中发挥重要作用。
Biochem J. 2007 Jan 15;401(2):377-90. doi: 10.1042/BJ20061432.
2
Protrusion force transmission of amoeboid cells crawling on soft biological tissue.在柔软生物组织上爬行的变形细胞的突出力传递
Acta Biomater. 2005 Sep;1(5):485-97. doi: 10.1016/j.actbio.2005.06.002. Epub 2005 Jul 26.
3
An iterative method to calculate forces exerted by single cells and multicellular assemblies from the detection of deformations of flexible substrates.一种通过检测柔性基板的变形来计算单个细胞和多细胞集合体所施加力的迭代方法。
Eur Biophys J. 2006 Apr;35(4):328-39. doi: 10.1007/s00249-005-0038-2. Epub 2006 Jan 11.
4
Direct mechanical force measurements during the migration of Dictyostelium slugs using flexible substrata.利用柔性基质在盘基网柄菌蛞蝓迁移过程中进行直接机械力测量。
Biophys J. 2005 Nov;89(5):3563-76. doi: 10.1529/biophysj.104.056333. Epub 2005 Aug 19.
5
Biochemistry and biomechanics of cell motility.细胞运动的生物化学与生物力学
Annu Rev Biomed Eng. 2005;7:105-50. doi: 10.1146/annurev.bioeng.7.060804.100340.
6
Talin B is required for force transmission in morphogenesis of Dictyostelium.Talin B在盘基网柄菌形态发生过程中的力传递中是必需的。
EMBO J. 2004 Jun 2;23(11):2216-25. doi: 10.1038/sj.emboj.7600238. Epub 2004 May 13.
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Cell migration: integrating signals from front to back.细胞迁移:整合从前到后的信号。
Science. 2003 Dec 5;302(5651):1704-9. doi: 10.1126/science.1092053.
8
Dictyostelium discoideum adhesion and motility under shear flow: experimental and theoretical approaches.盘基网柄菌在剪切流作用下的黏附与运动:实验与理论方法
J Muscle Res Cell Motil. 2002;23(7-8):651-8. doi: 10.1023/a:1024407107588.
9
Cross-linking of actin filaments by myosin II is a major contributor to cortical integrity and cell motility in restrictive environments.肌球蛋白II使肌动蛋白丝交联,这是在受限环境中维持皮质完整性和细胞运动的主要因素。
J Cell Sci. 2003 Sep 15;116(Pt 18):3761-70. doi: 10.1242/jcs.00684. Epub 2003 Jul 30.
10
Cellular motility driven by assembly and disassembly of actin filaments.由肌动蛋白丝的组装和解聚驱动的细胞运动。
Cell. 2003 Feb 21;112(4):453-65. doi: 10.1016/s0092-8674(03)00120-x.

通过改进的力细胞术对真核细胞运动性进行时空分析。

Spatio-temporal analysis of eukaryotic cell motility by improved force cytometry.

作者信息

Del Alamo Juan C, Meili Ruedi, Alonso-Latorre Baldomero, Rodríguez-Rodríguez Javier, Aliseda Alberto, Firtel Richard A, Lasheras Juan C

机构信息

Department of Mechanical and Aerospace Engineering, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 Aug 14;104(33):13343-8. doi: 10.1073/pnas.0705815104. Epub 2007 Aug 7.

DOI:10.1073/pnas.0705815104
PMID:17684097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1940228/
Abstract

Cell motility plays an essential role in many biological systems, but precise quantitative knowledge of the biophysical processes involved in cell migration is limited. Better measurements are needed to ultimately build models with predictive capabilities. We present an improved force cytometry method and apply it to the analysis of the dynamics of the chemotactic migration of the amoeboid form of Dictyostelium discoideum. Our explicit calculation of the force field takes into account the finite thickness of the elastic substrate and improves the accuracy and resolution compared with previous methods. This approach enables us to quantitatively study the differences in the mechanics of the migration of wild-type (WT) and mutant cell lines. The time evolution of the strain energy exerted by the migrating cells on their substrate is quasi-periodic and can be used as a simple indicator of the stages of the cell motility cycle. We have found that the mean velocity of migration v and the period of the strain energy T cycle are related through a hyperbolic law v = L/T, where L is a constant step length that remains unchanged in mutants with adhesion or contraction defects. Furthermore, when cells adhere to the substrate, they exert opposing pole forces that are orders of magnitude higher than required to overcome the resistance from their environment.

摘要

细胞运动性在许多生物系统中起着至关重要的作用,但对于细胞迁移所涉及的生物物理过程的精确量化知识却很有限。需要更好的测量方法来最终构建具有预测能力的模型。我们提出了一种改进的力细胞术方法,并将其应用于分析盘基网柄菌变形虫状形态趋化迁移的动力学。我们对力场进行的显式计算考虑了弹性基质的有限厚度,与先前的方法相比提高了准确性和分辨率。这种方法使我们能够定量研究野生型(WT)和突变细胞系迁移力学的差异。迁移细胞施加在其基质上的应变能的时间演化是准周期性的,可作为细胞运动周期阶段的一个简单指标。我们发现迁移平均速度v和应变能周期T通过双曲线定律v = L/T相关联,其中L是一个恒定步长,在有黏附或收缩缺陷的突变体中保持不变。此外,当细胞黏附在基质上时,它们会施加相反方向的极向力,这些力比克服其环境阻力所需力高出几个数量级。