Quantification of surface tension and internal pressure generated by single mitotic cells

被引:135
作者
Fischer-Friedrich, Elisabeth [1 ,2 ]
Hyman, Anthony A. [2 ]
Juelicher, Frank [1 ]
Mueller, Daniel J. [3 ]
Helenius, Jonne [3 ]
机构
[1] Max Planck Inst Phys Komplexer Syst, D-01187 Dresden, Germany
[2] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
[3] Eidgenoss TH Zurich, Dept Biosyst Sci & Engn, CH-4058 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
LIVING CELLS; SHAPE; MECHANICS; RETRACTION; INHIBITOR; MITOSIS; VOLUME; FLOW;
D O I
10.1038/srep06213
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
During mitosis, adherent cells round up, by increasing the tension of the contractile actomyosin cortex while increasing the internal hydrostatic pressure. In the simple scenario of a liquid cell interior, the surface tension is related to the local curvature and the hydrostatic pressure difference by Laplace's law. However, verification of this scenario for cells requires accurate measurements of cell shape. Here, we use wedged micro-cantilevers to uniaxially confine single cells and determine confinement forces while concurrently determining cell shape using confocal microscopy. We fit experimentally measured confined cell shapes to shapes obeying Laplace's law with uniform surface tension and find quantitative agreement. Geometrical parameters derived from fitting the cell shape, and the measured force were used to calculate hydrostatic pressure excess and surface tension of cells. We find that HeLa cells increase their internal hydrostatic pressure excess and surface tension from approximate to 40 Pa and 0.2 mNm(-1) during interphase to approximate to 400 Pa and 1.6 mNm(-1) during metaphase. The method introduced provides a means to determine internal pressure excess and surface tension of rounded cells accurately and with minimal cellular perturbation, and should be applicable to characterize the mechanical properties of various cellular systems.
引用
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页数:8
相关论文
共 45 条
[1]   Mammalian Cells Change Volume during Mitosis [J].
Boucrot, Emmanuel ;
Kirchhausen, Tomas .
PLOS ONE, 2008, 3 (01)
[2]   Life and times of a cellular bleb [J].
Charras, Guillaume T. ;
Coughlin, Margaret ;
Mitchison, Timothy J. ;
Mahadevan, L. .
BIOPHYSICAL JOURNAL, 2008, 94 (05) :1836-1853
[3]   Monitoring Actin Cortex Thickness in Live Cells [J].
Clark, Andrew G. ;
Dierkes, Kai ;
Paluch, Ewa K. .
BIOPHYSICAL JOURNAL, 2013, 105 (03) :570-580
[4]  
Clark AG, 2011, RESULTS PROBL CELL D, V53, P31, DOI 10.1007/978-3-642-19065-0_3
[5]   Surface forces of the Arbacia egg [J].
Cole, KS .
JOURNAL OF CELLULAR AND COMPARATIVE PHYSIOLOGY, 1932, 1 (01) :1-9
[6]   Investigation of the mechanism of retraction of the cell margin and rearward flow of nodules during mitotic cell rounding [J].
Cramer, LP ;
Mitchison, TJ .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (01) :109-119
[7]   Creep function of a single living cell [J].
Desprat, N ;
Richert, A ;
Simeon, J ;
Asnacios, A .
BIOPHYSICAL JOURNAL, 2005, 88 (03) :2224-2233
[8]   Mitosis-specific mechanosensing and contractile-protein redistribution control cell shape [J].
Effler, Janet C. ;
Kee, Yee-Seir ;
Berk, Jason M. ;
Tran, Minhchau N. ;
Iglesias, Pablo A. ;
Robinson, Douglas N. .
CURRENT BIOLOGY, 2006, 16 (19) :1962-1967
[10]  
EVANS E, 1984, BLOOD, V64, P1028