Abstract
The mechanical behavior of cells is connected to cell functions involving the cytoskeleton, like contractility, motility, and proliferation, which are essential for the skin’s homeostasis.
Changes in mechanical properties are an important characteristic of the aging process of the human skin. Studies attribute these changes predominately to the extracellular matrix (ECM) due to its altered collagen and elastin organization and density. Nevertheless, individual skin cells can also show significant changes in stiffness, which can be measured by sophisticated tools like the laser-based optical cell stretcher that allows examining the viscoelastic biomechanics of isolated cells. As compared to other techniques for single cell elasticity measurements such as scanning-force microscopy (SFM), an optical stretcher enables the measurement of more than a hundred cells per hour providing advanced statistical results.
Abbreviations
- ECM:
-
Extracellular matrix
- SFM:
-
Scanning-force microscopy
References
Ashkin A. Acceleration and trapping of particles by radiation pressure. Phys Rev Lett. 1970;24(4):156–9.
Ashkin A, Dziedzic JM. Radiation pressure on a free liquid surface. Phys Rev Lett. 1973;30(4):139–42.
Ashkin A, Dziedzic JM, Yamane T. Optical trapping and manipulation of single cells using infrared laser beams. Nature. 1987;330(6150):769–71.
Bereiter-Hahn J, Lüers H. In: Akkas N, editor. Biomechanics of active movement and division of cells. Berlin: Springer; 1994. p. 181–230.
Boudou T, Ohayon J, Picart C, Pettigrew RI, Tracqui P. Nonlinear elastic properties of polyacrylamide gels: implications for quantification of cellular forces. Biorheology. 2009;46(3):191–205.
Brown RA, Talas G, Porter RA, McGrouther DA, Eastwood M. Balanced mechanical forces and microtubule contribution to fibroblast contraction. J Cell Physiol. 1996;169(3):439–47.
Fabry B, et al. Scaling the microrheology of living cells. Phys Rev Lett. 2001;87(14):148102.
Fernandez P, Heymann L, Ott A, Aksel N, Pullarkat PA. Shear rheology of a cell monolayer. New J Phys. 2007;9:419.
Fletcher DA, Mullins RD. Cell mechanics and the cytoskeleton. Nature. 2010;463(7280):485–92.
Fluck M, Giraud M-N, Tunc V, Chiquet M. Tensile stress-dependent collagen XII and fibronectin production by fibroblasts requires separate pathways. Biochim Biophys Acta. 2003;1593:239–48.
Guck J, Ananthakrishnan R, Moon TJ, Cunningham CC, Käs J. Optical deformability of soft biological dielectrics. Phys Rev Lett. 2000;84(23):5451–4.
Hertz H. Über die Berührung fester elastischer Körper. J Reine Angew Math. 1881;92:156–71.
Hochmuth RM. Micropipette aspiration of living cells. J Biomech. 2000;33:15–22.
Ingber DE. Tensegrity: the architectural basis of cellular mechanotransduction. Annu Rev Physol. 1997;59:575–99.
Janmey PA, Weitz DA. Dealing with mechanics: mechanisms of force transduction in cells. Trends Biochem Sci. 2004;29(7):364–70.
Kessler D, Dethlefsen S, Haase I, Plomann M, Hirche F, Krieg T, Eckes B. Fibroblasts in mechanically stressed collagen lattices assume a “synthetic” phenotype. J Biol Chem. 2001;237:159–72.
Kollmannsberger P, Fabry B. Active soft glassy rheology of adherent cells. Soft Matter. 2009;5:1771–4.
Kolodney MS, Wysolmerski RB. Isometric contraction by fibroblasts and endothelial cells in tissue culture: a quantitative study. J Cell Biol. 1992;117:73–82.
Mahaffy RE, Shih CK, MacKintosh FC, Käs J. Scanning probe-based frequency-dependent microrheology of polymer gels and biological cells. Phys Rev Lett. 2000;85(4):880–3.
Rotsch C, Radmacher M. Drug-induced changes of cytoskeletal structure and mechanics in fibroblasts: an atomic force microscopy study. Biophys J. 2000;78(1):520–35.
Schulze C, Wetzel F, Kueper T, Malsen A, Muhr G, Jaspers S, Blatt T, Wittern KP, Wenck H, Käs JA. Stiffening of human skin fibroblasts with age. Biophys J. 2010;99(8):2434–42.
Semmrich C, Storz T, Glaser J, Merkel R, Bausch AR, Kroy K. Glass transition and rheological redundancy in F-actin solutions. Proc Natl Acad Sci U S A. 2007;104(51):20199–203.
Sleep J, Wilson D, Simmons R, Gratzer W. Elasticity of the red cell membrane and its relation to hemolytic disorders: an optical tweezers study. Biophys J. 1999;77:3085–95.
Sung KL, Yang L, Whittemore DE, Shi Y, Jin G, Hsieh AH, Akeson WH, Sung LA. The differential adhesion forces of anterior cruciate and medial collateral ligament fibroblasts: effects of tropomodulin, talin, vinculin, and alpha-actinin. Proc Natl Acad Sci U S A. 1996;93(17):9182–7.
Ward KA, Li WI, Zimmer S, Davis T. Viscoelastic properties of transformed cells: role in tumor cell progression and metastasis formation. Biorheology. 1991;28:301–13.
Wottawah F, Schinkinger S, Lincoln B, Ananthakrishnan R, Romeyke M, Guck J, Käs J. Optical rheology of biological cells. Phys Rev Lett. 2005a;94(9):098103.
Wottawah F, Schinkinger S, Lincoln B, Ebert S, Müller K, Sauer F, Travis K, Guck J. Characterizing single suspended cells by optorheology. Acta Biomater. 2005b;1(1):263–27.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer International Publishing Switzerland
About this entry
Cite this entry
Schulze, C., Jaspers, S. (2015). Measuring Skin Cell Stiffness. In: Humbert, P., Maibach, H., Fanian, F., Agache, P. (eds) Agache’s Measuring the Skin. Springer, Cham. https://doi.org/10.1007/978-3-319-26594-0_147-1
Download citation
DOI: https://doi.org/10.1007/978-3-319-26594-0_147-1
Received:
Accepted:
Published:
Publisher Name: Springer, Cham
Online ISBN: 978-3-319-26594-0
eBook Packages: Springer Reference MedicineReference Module Medicine