Abstract
By using magnetic bead microrheology we study the effect of inflammatory agents and toxins on the viscoelastic moduli of endothelial cell plasma membranes in real time. Viscoelastic response curves were acquired by applying short force pulses of ~500 pN to fibronectin-coated magnetic beads attached to the surface membrane of endothelial cells. Upon addition of thrombin, a rapid stiffening of the membrane was observed within 5 s, followed by recovery of the initial deformability within 2 min. By using specific inhibitors, two known pathways by which thrombin induces actin reorganization in endothelial cells, namely activation of Ca2+-calmodulin-dependent myosin light chain kinase and stimulation of Rho/Rho-kinase, were excluded as possible causes of the stiffening effect. Interestingly, the cytotoxic necrotizing factor of Escherichia coli, a toxin which, in addition to Rho, activates the GTPases Rac and CDC42Hs, also induced a dramatic stiffening effect, suggesting that the stiffening may be mediated through a Rac- or Cdc42Hs-dependent pathway. This work demonstrates that magnetic bead microrheometry is not only a powerful tool to determine the absolute viscoelastic moduli of the composite cell plasma membrane, but also a valuable tool to study in real time the effect of drugs or toxins on the viscoelastic parameters of the plasma membrane.
Full Text
The Full Text of this article is available as a PDF (255.4 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aepfelbacher M., Essler M., Huber E., Czech A., Weber P. C. Rho is a negative regulator of human monocyte spreading. J Immunol. 1996 Dec 1;157(11):5070–5075. [PubMed] [Google Scholar]
- Allen W. E., Jones G. E., Pollard J. W., Ridley A. J. Rho, Rac and Cdc42 regulate actin organization and cell adhesion in macrophages. J Cell Sci. 1997 Mar;110(Pt 6):707–720. doi: 10.1242/jcs.110.6.707. [DOI] [PubMed] [Google Scholar]
- Ashkin A. Optical trapping and manipulation of neutral particles using lasers. Proc Natl Acad Sci U S A. 1997 May 13;94(10):4853–4860. doi: 10.1073/pnas.94.10.4853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bausch A. R., Möller W., Sackmann E. Measurement of local viscoelasticity and forces in living cells by magnetic tweezers. Biophys J. 1999 Jan;76(1 Pt 1):573–579. doi: 10.1016/S0006-3495(99)77225-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bausch A. R., Ziemann F., Boulbitch A. A., Jacobson K., Sackmann E. Local measurements of viscoelastic parameters of adherent cell surfaces by magnetic bead microrheometry. Biophys J. 1998 Oct;75(4):2038–2049. doi: 10.1016/S0006-3495(98)77646-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bodmer J. E., Van Engelenhoven J., Reyes G., Blackwell K., Kamath A., Shasby D. M., Moy A. B. Isometric tension of cultured endothelial cells: new technical aspects. Microvasc Res. 1997 May;53(3):261–271. doi: 10.1006/mvre.1997.2011. [DOI] [PubMed] [Google Scholar]
- Chicurel M. E., Singer R. H., Meyer C. J., Ingber D. E. Integrin binding and mechanical tension induce movement of mRNA and ribosomes to focal adhesions. Nature. 1998 Apr 16;392(6677):730–733. doi: 10.1038/33719. [DOI] [PubMed] [Google Scholar]
- Essler M., Amano M., Kruse H. J., Kaibuchi K., Weber P. C., Aepfelbacher M. Thrombin inactivates myosin light chain phosphatase via Rho and its target Rho kinase in human endothelial cells. J Biol Chem. 1998 Aug 21;273(34):21867–21874. doi: 10.1074/jbc.273.34.21867. [DOI] [PubMed] [Google Scholar]
- Essler M., Retzer M., Bauer M., Heemskerk J. W., Aepfelbacher M., Siess W. Mildly oxidized low density lipoprotein induces contraction of human endothelial cells through activation of Rho/Rho kinase and inhibition of myosin light chain phosphatase. J Biol Chem. 1999 Oct 22;274(43):30361–30364. doi: 10.1074/jbc.274.43.30361. [DOI] [PubMed] [Google Scholar]
- Garcia J. G., Schaphorst K. L. Regulation of endothelial cell gap formation and paracellular permeability. J Investig Med. 1995 Apr;43(2):117–126. [PubMed] [Google Scholar]
- Hartwig J. H., Bokoch G. M., Carpenter C. L., Janmey P. A., Taylor L. A., Toker A., Stossel T. P. Thrombin receptor ligation and activated Rac uncap actin filament barbed ends through phosphoinositide synthesis in permeabilized human platelets. Cell. 1995 Aug 25;82(4):643–653. doi: 10.1016/0092-8674(95)90036-5. [DOI] [PubMed] [Google Scholar]
- Higgs H. N., Pollard T. D. Regulation of actin polymerization by Arp2/3 complex and WASp/Scar proteins. J Biol Chem. 1999 Nov 12;274(46):32531–32534. doi: 10.1074/jbc.274.46.32531. [DOI] [PubMed] [Google Scholar]
- Jalink K., van Corven E. J., Hengeveld T., Morii N., Narumiya S., Moolenaar W. H. Inhibition of lysophosphatidate- and thrombin-induced neurite retraction and neuronal cell rounding by ADP ribosylation of the small GTP-binding protein Rho. J Cell Biol. 1994 Aug;126(3):801–810. doi: 10.1083/jcb.126.3.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kolodney M. S., Wysolmerski R. B. Isometric contraction by fibroblasts and endothelial cells in tissue culture: a quantitative study. J Cell Biol. 1992 Apr;117(1):73–82. doi: 10.1083/jcb.117.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lampugnani M. G., Corada M., Caveda L., Breviario F., Ayalon O., Geiger B., Dejana E. The molecular organization of endothelial cell to cell junctions: differential association of plakoglobin, beta-catenin, and alpha-catenin with vascular endothelial cadherin (VE-cadherin). J Cell Biol. 1995 Apr;129(1):203–217. doi: 10.1083/jcb.129.1.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lerm M., Selzer J., Hoffmeyer A., Rapp U. R., Aktories K., Schmidt G. Deamidation of Cdc42 and Rac by Escherichia coli cytotoxic necrotizing factor 1: activation of c-Jun N-terminal kinase in HeLa cells. Infect Immun. 1999 Feb;67(2):496–503. doi: 10.1128/iai.67.2.496-503.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miyamoto S., Akiyama S. K., Yamada K. M. Synergistic roles for receptor occupancy and aggregation in integrin transmembrane function. Science. 1995 Feb 10;267(5199):883–885. doi: 10.1126/science.7846531. [DOI] [PubMed] [Google Scholar]
- Miyamoto S., Katz B. Z., Lafrenie R. M., Yamada K. M. Fibronectin and integrins in cell adhesion, signaling, and morphogenesis. Ann N Y Acad Sci. 1998 Oct 23;857:119–129. doi: 10.1111/j.1749-6632.1998.tb10112.x. [DOI] [PubMed] [Google Scholar]
- Raucher D., Stauffer T., Chen W., Shen K., Guo S., York J. D., Sheetz M. P., Meyer T. Phosphatidylinositol 4,5-bisphosphate functions as a second messenger that regulates cytoskeleton-plasma membrane adhesion. Cell. 2000 Jan 21;100(2):221–228. doi: 10.1016/s0092-8674(00)81560-3. [DOI] [PubMed] [Google Scholar]
- Schmidt G., Sehr P., Wilm M., Selzer J., Mann M., Aktories K. Gln 63 of Rho is deamidated by Escherichia coli cytotoxic necrotizing factor-1. Nature. 1997 Jun 12;387(6634):725–729. doi: 10.1038/42735. [DOI] [PubMed] [Google Scholar]
- Yamada K. M., Geiger B. Molecular interactions in cell adhesion complexes. Curr Opin Cell Biol. 1997 Feb;9(1):76–85. doi: 10.1016/s0955-0674(97)80155-x. [DOI] [PubMed] [Google Scholar]
- Ziemann F., Rädler J., Sackmann E. Local measurements of viscoelastic moduli of entangled actin networks using an oscillating magnetic bead micro-rheometer. Biophys J. 1994 Jun;66(6):2210–2216. doi: 10.1016/S0006-3495(94)81017-3. [DOI] [PMC free article] [PubMed] [Google Scholar]