Measurement of the thickness and volume of adherent cells using transmission-through-dye microscopy

Cell volume is one of the basic characteristics of a cell and is being extensively studied in relationship to a variety of processes, such as proliferation, apoptosis, fertility, or locomotion. At the same time, its measurement under a microscope has not been well developed. The method we propose uses negative transmission contrast rendered to cells by a strongly absorbing dye present in the extracellular medium. Cells are placed in a shallow compartment, and a nontoxic and cell-impermeant dye, such as acid blue 9, is added to the medium. Transmission images are collected at the wavelength of maximum dye absorption (630 nm). Where the cell body displaces the dye, the thickness of the absorbing layer is reduced; thus, an increase in cell thickness produces brighter images and vice versa. The absolute values for cell thickness and volume can be easily extracted from the image by computing the logarithm of intensity and dividing it by the absorption coefficient. The method is fast, impervious to instability of the light source, and has a high signal-to-noise ratio; it can be realized either on a laser scanning or a conventional microscope equipped with a bandpass filter. For long-term experiments, we use a Bioptechs perfusion chamber fitted with a 0.03-mm spacer and an additional port to enable rapid switching of solutions. To show possible applications of this method, we investigated the kinetics of the cell volume response to a hypotonic buffer and to the apoptotic agents staurosporine and ionomycin.

[1]  B. Wiesner,et al.  Cell volume kinetics of adherent epithelial cells measured by laser scanning reflection microscopy: determination of water permeability changes of renal principal cells. , 2001, Biophysical journal.

[2]  F. Wehner,et al.  Subunits α, β and γ of the epithelial Na+ channel (ENaC) are functionally related to the hypertonicity-induced cation channel (HICC) in rat hepatocytes , 2007, Pflügers Archiv - European Journal of Physiology.

[3]  M. Jacquin,et al.  Calcium ionophores can induce either apoptosis or necrosis in cultured cortical neurons , 1999, Neuroscience.

[4]  A. Verkman,et al.  Water Permeability Measurement in Living Cells and Complex Tissues , 2000, The Journal of Membrane Biology.

[5]  D. Fletcher,et al.  Giardia lamblia Attachment Force Is Insensitive to Surface Treatments , 2006, Eukaryotic Cell.

[6]  S. Doglia,et al.  Technical report: Cell thickness measurements by confocal fluorescence microscopy on C3H10T1/2 and V79 cells. , 1998, International journal of radiation biology.

[7]  T. Hanafusa,et al.  Delayed shrinkage triggered by the Na+–K+ pump in terbutaline‐stimulated rat alveolar type II cells , 2004, Experimental physiology.

[8]  Y. Kanno,et al.  Survival of BSC-1 cells through the maintenance of cell volume brought about by epidermal growth factor depends on attachment to the substratum , 1990, Experientia.

[9]  J. Mege,et al.  Study of cell deformability by a simple method. , 1985, Journal of immunological methods.

[10]  M. Leippe,et al.  Necrosis versus apoptosis as the mechanism of target cell death induced by Entamoeba histolytica , 1997, Infection and immunity.

[11]  J. E. Melvin,et al.  The NHX Family of Na+-H+ Exchangers in Caenorhabditis elegans * , 2002, The Journal of Biological Chemistry.

[12]  M J Lab,et al.  Cell volume measurement using scanning ion conductance microscopy. , 2000, Biophysical journal.

[13]  A. Verkman,et al.  Constitutive and regulated membrane expression of aquaporin 1 and aquaporin 2 water channels in stably transfected LLC-PK1 epithelial cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[14]  Ling Wei,et al.  Effects of chloride and potassium channel blockers on apoptotic cell shrinkage and apoptosis in cortical neurons , 2004, Pflügers Archiv.

[15]  Milan Mrksich,et al.  Micropatterned Surfaces for Control of Cell Shape, Position, and Function , 1998, Biotechnology progress.

[16]  D. Jelinek,et al.  Differential activation of a calcium-dependent endonuclease in human B lymphocytes. Role in ionomycin-induced apoptosis. , 1995, Journal of immunology.

[17]  S. Huang,et al.  Shape-dependent control of cell growth, differentiation, and apoptosis: switching between attractors in cell regulatory networks. , 2000, Experimental cell research.

[18]  Takahiro Shimizu,et al.  Receptor‐mediated control of regulatory volume decrease (RVD) and apoptotic volume decrease (AVD) , 2001, The Journal of physiology.

[19]  F. Schliess,et al.  The hepatocyte integrin system and cell volume sensing , 2006, Acta physiologica.

[20]  Simion I. Chiosea,et al.  Inducible changes in cell size and attachment area due to expression of a mutant SWI/SNF chromatin remodeling enzyme , 2004, Journal of Cell Science.

[21]  A. Akaike,et al.  Thrombin-induced delayed injury involves multiple and distinct signaling pathways in the cerebral cortex and the striatum in organotypic slice cultures , 2006, Neurobiology of Disease.

[22]  D. Häussinger,et al.  The role of calcium in cell shrinkage and intracellular alkalinization by bradykinin in Ha‐ras oncogene expressing cells , 1993, FEBS letters.

[23]  F. Lang,et al.  Cell volume regulatory mechanisms. , 2006, Contributions to nephrology.

[24]  R. Grygorczyk,et al.  Cell swelling‐induced ATP release is tightly dependent on intracellular calcium elevations , 2004, The Journal of physiology.

[25]  R. Gazzinelli,et al.  Cell surface fluctuations studied with defocusing microscopy. , 2003, Physical review. E, Statistical, nonlinear, and soft matter physics.

[26]  R. Wepf,et al.  Noninvasive measurement of cell volume changes by negative staining. , 2005, Journal of biomedical optics.

[27]  Hjalmar Brismar,et al.  Osmotic water permeability measurements using confocal laser scanning microscopy , 2000, European Biophysics Journal.

[28]  F. Lang,et al.  Cell volume and the regulation of apoptotic cell death , 2004, Journal of Molecular Recognition.

[29]  R. Bindels,et al.  Measuring volume perturbation of proximal tubular cells in primary culture with three different techniques. , 1996, The American journal of physiology.

[30]  M. Model,et al.  Measurement of the absorption of concentrated dyes and their use for quantitative imaging of surface topography , 2008, Journal of microscopy.

[31]  K. Kohn,et al.  Induction of a common pathway of apoptosis by staurosporine. , 1994, Experimental cell research.

[32]  Takahiro Shimizu,et al.  Prerequisite role of persistent cell shrinkage in apoptosis of human epithelial cells. , 2007, Sheng li xue bao : [Acta physiologica Sinica].

[33]  T. Borg,et al.  The Expression and Role of Protein Kinase C in Neonatal Cardiac Myocyte Attachment, Cell Volume, and Myofibril Formation Is Dependent on the Composition of the Extracellular Matrix , 2005, Microscopy and Microanalysis.

[34]  Christine Evrard,et al.  Cell volume changes during rapid temperature shifts. , 2003, Journal of biotechnology.

[35]  D. Epstein,et al.  Expression of aquaporin-1 in human trabecular meshwork cells: role in resting cell volume. , 2001, Investigative ophthalmology & visual science.

[36]  M. Gunaratnam,et al.  Damage to F-actin and cell death induced by chromium VI and nickel in primary monolayer cultures of rat hepatocytes. , 2004, Toxicology in vitro : an international journal published in association with BIBRA.

[37]  Oliver Popp,et al.  Ionomycin-activated Calpain Triggers Apoptosis , 2002, The Journal of Biological Chemistry.

[38]  S. Nielsen,et al.  Expression and immunolocalization of aquaporin water channels in rat exocrine pancreas. , 2001, American journal of physiology. Gastrointestinal and liver physiology.

[39]  J. Loike,et al.  Evidence that the glucose transporter serves as a water channel in J774 macrophages. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[40]  M. Lisanti,et al.  Caveolin-1 expression sensitizes fibroblastic and epithelial cells to apoptotic stimulation. , 2001, American journal of physiology. Cell physiology.

[41]  F. Alvarez-Leefmans,et al.  Volume changes in single N1E-115 neuroblastoma cells measured with a fluorescent probe , 1995, Neuroscience.

[42]  Staurosporine Induces Apoptotic Volume Decrease (AVD) in ECV304 Cells , 2003, Annals of the New York Academy of Sciences.

[43]  T. Litman,et al.  Measurement of Cell Volume Changes by Fluorescence Self-Quenching , 2002, Journal of Fluorescence.

[44]  H. J. van Elburg,et al.  Improved correction of axial geometrical distortion in index‐mismatched fluorescent confocal microscopic images using high‐aperture objective lenses , 2007, Journal of microscopy.

[45]  G. Krumschnabel,et al.  Staurosporine-induced cell death in salmonid cells: the role of apoptotic volume decrease, ion fluxes and MAP kinase signaling , 2007, Apoptosis.

[46]  Y Ishizaki,et al.  Normotonic cell shrinkage because of disordered volume regulation is an early prerequisite to apoptosis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[47]  S. P. Srinivas,et al.  Measurement of rapid changes in cell volume by forward light scattering , 2003, Pflügers Archiv.

[48]  S. Grinstein,et al.  Cytoplasmic [Ca2+] and intracellular pH in lymphocytes. Role of membrane potential and volume-activated Na+/H+ exchange , 1987, The Journal of general physiology.

[49]  G. Capasso,et al.  Mechanisms and clinical significance of cell volume regulation. , 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[50]  A. Morgan,et al.  Ionomycin enhances Ca2+ influx by stimulating store-regulated cation entry and not by a direct action at the plasma membrane. , 1994, The Biochemical journal.

[51]  Y. Korchev,et al.  Spatial distribution of maxi-anion channel on cardiomyocytes detected by smart-patch technique. , 2008, Biophysical journal.

[52]  R. Grygorczyk,et al.  Evaluation of rapid volume changes of substrate‐adherent cells by conventional microscopy 3D imaging , 2004, Journal of microscopy.

[53]  Y. Ito,et al.  Surface micropatterning to regulate cell functions. , 1999, Biomaterials.

[54]  M. Sheetz,et al.  Local force and geometry sensing regulate cell functions , 2006, Nature Reviews Molecular Cell Biology.