journal article·2013-07Open access

Silicon chips detect intracellular pressure changes in living cells

Rodrigo Gómez-Martínez, Alberto M. Hernández-Pinto, Marta Duch, Patricia Vázquez, Kirill Zinoviev, Enrique J. de la Rosa, Jaume Esteve, Teresa Suárez, José A. Plaza

Nature Nanotechnology· Volume 8· Issue 7

Abstract

The ability to measure pressure changes inside different components of a living cell is important, because it offers an alternative way to study fundamental processes that involve cell deformation. Most current techniques such as pipette aspiration, optical interferometry or external pressure probes use either indirect measurement methods or approaches that can damage the cell membrane. Here we show that a silicon chip small enough to be internalized into a living cell can be used to detect pressure changes inside the cell. The chip, which consists of two membranes separated by a vacuum gap to form a Fabry-Pérot resonator, detects pressure changes that can be quantified from the intensity of the reflected light. Using this chip, we show that extracellular hydrostatic pressure is transmitted into HeLa cells and that these cells can endure hypo-osmotic stress without significantly increasing their intracellular hydrostatic pressure.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Cellular Mechanics and Interactions · Mechanical and Optical Resonators · Advanced Fluorescence Microscopy Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (30)

Show source-provided references
1. Stewart, M. P. et al. Hydrostatic pressure and the actomyosin cortex drive mitotic cell rounding. Nature 469, 226–230 (2011).10.1038/nature09642 ↗
2. Rand, R. P. & Burton, A. C. Mechanical properties of red cell membrane. i. Membrane stiffness+intracellular pressure. Biophys. J. 4, 115–135 (1964).10.1016/S0006-3495(64)86773-4 ↗
3. Strohmeier, R. & Bereiterhahn, J. Hydrostatic-pressure in epidermal-cells is dependent on Ca-mediated contractions. J. Cell Sci. 88, 631–640 (1987).10.1242/jcs.88.5.631 ↗
4. Kelly, S. M. & Macklem, P. T. Direct measurement of intracellular pressure. Am. J. Physiol. 260, C652–C657 (1991).10.1152/ajpcell.1991.260.3.C652 ↗
5. Whitesides, G. M. The ‘right’ size in nanobiotechnology. Nature Biotechnol. 21, 1161–1165 (2003).10.1038/nbt872 ↗
6. Singhal, R. et al. Multifunctional carbon-nanotube cellular endoscopes. Nature Nanotech. 6, 57–63 (2011).10.1038/nnano.2010.241 ↗
7. Tian, B. Z. et al. Three-dimensional, flexible nanoscale field-effect transistors as localized bioprobes. Science 329, 830–834 (2010).10.1126/science.1192033 ↗
8. Arlett, J. L., Myers, E. B. & Roukes, M. L. Comparative advantages of mechanical biosensors. Nature Nanotech. 6, 203–215 (2011).10.1038/nnano.2011.44 ↗
9. Cross, S. E., Jin, Y. S., Rao, J. & Gimzewski, J. K. Nanomechanical analysis of cells from cancer patients. Nature Nanotech. 2, 780–783 (2007).10.1038/nnano.2007.388 ↗
10. Balaban, N. Q. et al. Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates. Nature Cell Biol. 3, 466–472 (2001).10.1038/35074532 ↗
11. Vaziri, A. & Gopinath, A. Cell and biomolecular mechanics in silico. Nature Mater. 7, 15–23 (2008).10.1038/nmat2040 ↗
12. Fan, J. Y. & Chu, P. K. Group IV nanoparticles: synthesis, properties, and biological applications. Small 6, 2080–2098 (2010).10.1002/smll.201000543 ↗
13. Tasciotti, E. et al. Mesoporous silicon particles as a multistage delivery system for imaging and therapeutic applications. Nature Nanotech. 3, 151–157 (2008).10.1038/nnano.2008.34 ↗
14. Fernandez-Rosas, E. et al. Intracellular polysilicon barcodes for cell tracking. Small 5, 2433–2439 (2009).10.1002/smll.200900733 ↗
15. Novo, S. et al. A novel embryo identification system by direct tagging of mouse embryos using silicon-based barcodes. Human Reprod. 26, 96–105 (2011).10.1093/humrep/deq309 ↗
16. Gomez-Martinez, R. et al. Intracellular silicon chips in living cells. Small 6, 499–502 (2010).10.1002/smll.200901041 ↗
17. Born, M. & Wolf, E. Principles of Optics 6th edn (Pergamon, 1980).
18. French, P. J. Polysilicon: a versatile material for microsystems. Sens. Actuat. A 99, 3–12 (2002).10.1016/S0924-4247(01)00876-7 ↗
19. Myers, K. A., Rattner, J. B., Shrive, N. G. & Hart, D. A. Hydrostatic pressure sensation in cells: integration into the tensegrity model. Biochem. Cell Biol. 85, 543–551 (2007).10.1139/O07-108 ↗
20. Ingber, D. E. & Tensegrity I. Cell structure and hierarchical systems biology. J. Cell Sci. 116, 1157–1173 (2003).10.1242/jcs.00359 ↗
21. Borgnia, M., Nielsen, S., Engle, A. & Agre, P. Cellular and molecular biology of the aquaporin water channels. Annu. Rev. Biochem. 68, 425–458 (1999).10.1146/annurev.biochem.68.1.425 ↗
22. Spagnoli, C., Beyder, A., Besch, S. & Sachs, F. Atomic force microscopy analysis of cell volume regulation. Phys. Rev. E 78, 031916 (2008).10.1103/PhysRevE.78.031916 ↗
23. Finan, J. D. & Guilak, F. The effects of osmotic stress on the structure and function of the cell nucleus. J. Cell Biochem. 109, 460–467 (2010).10.1002/jcb.22437 ↗
24. Pietuch, A, Brückner, B. R. & Janshoff, A. Membrane tension homeostasis of epithelial cells through surface area regulation in response to osmotic stress. Biochim. Biophys. Acta Mol. Cell Res. 1833, 712–722 (2013).10.1016/j.bbamcr.2012.11.006 ↗
25. Tambe, D. T. et al. Collective cell guidance by cooperative intercellular forces. Nature Mater. 10, 469–475 (2011).10.1038/nmat3025 ↗
26. Trepat, X. et al. Physical forces during collective cell migration. Nature Phys. 5, 426–430 (2009).10.1038/nphys1269 ↗
27. DuFort, C. C., Paszek, M. J. & Weaver, V. M. Balancing forces: architectural control of mechanotransduction. Nature Rev. Mol. Cell Biol. 12, 308–318 (2011).10.1038/nrm3112 ↗
28. Jaalouk, D. E. & Lammerding, J. Mechanotransduction gone awry. Nature Rev. Mol. Cell Biol. 10, 63–73 (2009).10.1038/nrm2597 ↗
29. Fritsch, A. et al. Are biomechanical changes necessary for tumour progression? Nature Phys. 6, 730–732 (2010).10.1038/nphys1800 ↗
30. Wozniak, M. A. & Chen, C. S. Mechanotransduction in development: a growing role for contractility. Nature Rev. Mol. Cell Biol. 10, 34–43 (2009).10.1038/nrm2592 ↗