Laser light-scattering system for studying cell volume regulation and membrane transport processes

1993 ◽  
Vol 265 (2) ◽  
pp. C562-C570 ◽  
Author(s):  
M. McManus ◽  
J. Fischbarg ◽  
A. Sun ◽  
S. Hebert ◽  
K. Strange

A simple and relatively inexpensive device utilizing laser light scattering for the study of volume regulatory behavior and membrane transport phenomena in cells cultured on or affixed to a rigid substrate is described in detail. Validation of the method is provided by study of cell types with known volume regulatory responses. The method we describe has numerous advantages over currently available techniques used to monitor cell volume changes. These advantages include 1) the ability to rapidly detect and quantify small cell volume changes on-line, 2) the ability to maintain natural cell morphology, cell surface contacts, and cell-to-cell interactions, 3) the ability to easily control solution temperature and gas and solute composition, and 4) the ability to perform multiple perturbations in a single experiment. The light-scattering system we describe can be modified to allow for simultaneous measurement of light-scattering signals and fluorescence emission from intracellular ion-sensitive probes and membrane potential dyes. In addition, our method may be useful for the study of apical and basolateral membrane transport processes in epithelial monolayer cell cultures.

Author(s):  
Arturo Moreno-Baez ◽  
Gerardo Miramontes-de Leon ◽  
Claudia Sifuentes-Gallardo ◽  
Ernesto Garcia-Dominguez ◽  
Daniel Alaniz-Lumbreras ◽  
...  

1993 ◽  
Vol 4 (2) ◽  
pp. 215-220 ◽  
Author(s):  
E A Perkins ◽  
R J G Carr ◽  
J Rarity ◽  
K Chow ◽  
T Atkinson

1985 ◽  
Vol 23 (3) ◽  
pp. 263-268 ◽  
Author(s):  
J. C. Earnshaw ◽  
G. Munroe ◽  
W. Thompson ◽  
A. I. Traub

1988 ◽  
Vol 36 (12) ◽  
pp. 4951-4957 ◽  
Author(s):  
SUMIE YOSHIOKA ◽  
KAZUO IWAKI ◽  
YUZURU HAYASHI ◽  
YUKIO ASO ◽  
YASUSHI TAKEDA ◽  
...  

2012 ◽  
Vol 6 (4) ◽  
pp. 1188-1195 ◽  
Author(s):  
Berenice Yahuaca-Juárez ◽  
Juan de Dios Ortíz-Alvarado ◽  
Héctor Eduardo Martínez-Flores ◽  
Reynaldo C. Pless ◽  
Pedro A. Vázquez-Landaverde ◽  
...  

Blood ◽  
1986 ◽  
Vol 68 (2) ◽  
pp. 506-513 ◽  
Author(s):  
N Mohandas ◽  
YR Kim ◽  
DH Tycko ◽  
J Orlik ◽  
J Wyatt ◽  
...  

Cell volume (MCV) and hemoglobin concentration (MCHC) are the red cell indices used to characterize the blood of patients with anemia. Since the introduction of flow cytometric methods for the measurement of these indices, it has generally been assumed that the values derived by these instruments are accurate. However, it has recently been shown that a number of cellular factors, including alterations in cellular deformability, can lead to inaccurate measurement of cell volume by these automated instruments. Because cell hemoglobin concentration and hematocrit are computed from the measured values of cell volume, accuracy of these indices is also compromised by inaccurate determination of cell volume. A recently developed experimental flow cytometric method based on laser light scattering, which can independently measure volume and hemoglobin concentration, has been used in the present study to measure MCV and MCHC of density- fractionated normal and sickle red cells, hydrated and dehydrated normal red cells, and various pathologic cells. We found that the new method accurately measures both volume and hemoglobin concentrations over a wide range of MCV (30 to 120 fL) and MCHC (27 to 45 g/dL) values. This is in contrast to currently available methods in which hemoglobin concentration values are accurately measured over a more limited range (27 to 35 g/dL). In addition, as the experimental method independently measures volume and hemoglobin concentration of individual red cells, it allowed us to generate histograms of volume and hemoglobin concentration distribution and derive coefficient of variation for volume distribution and standard deviation of hemoglobin concentration distribution. We have been able to document that volume and hemoglobin concentration distributions can vary independently of each other in pathologic red cell samples.


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