Method Article

Counting Human Neural Stem Cells

DOI:

10.3791/262

August 22nd, 2007

In This Article

Summary

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Knowledge of the exact number of viable cells is required for many tissue culture manipulations. This protocol describes how to differentiate between live and dead cells and quantify cells using a hemacytometer. Although it describes counting human neural stem/precursor cells (hNSPCs), it can be used for other cell types.

Abstract

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Knowledge of the exact number of viable cells in a given volume of a cell suspension is required for many routine tissue culture manipulations, such as plating cells for immunocytochemistry or for cell transfections. This protocol describes a straightforward and fast method for differentiating between live and dead cells and quantifying the cell concentration and total cell number using a hemacytometer. This procedure first requires detaching cells from a growth surface and resuspending them in media. Next, the cells are diluted in a solution of Trypan blue (ideally to a concentration that will give 20-50 cells per quadrant) and placed in the hemacytometer. Finally, averaging the counts of viable cells in several randomly selected quadrants, dividing the average by the volume of one 1 mm2 quadrant (0.1 μl) and multiplying by the dilution factor gives the number of cells per l. Multiplying this cell concentration by the total volume in μl gives the total cell number. This protocol describes counting human neural stem/precursor cells (hNSPCs), but can also be used for many other cell types.

Protocol

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Passaging Human Neural Stem Cells

Note: Please refer to the Passaging Human Neural Stem Cells article on how to detach and resuspend the cells. https://www.jove.com/index/Details.stp?ID=263

Preparing the Cell Suspension for Counting

  1. Place 25 µl of 0.4% Trypan Blue solution and 20 µl of cell media into an eppendorf tube.
  2. Resuspend the cells to be counted by gently tapping the tube containing the cells in a known volume of media to create a homogenous suspensio....

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Discussion

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This protocol describes a straightforward and rapid way to determine the cell concentration for a variety of experiments involving cells. Using the shortcut described in 3d, one can quickly and accurately determine the cell concentration and total cell number in a given volume.

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Acknowledgements

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The authors would like to acknowledge Dr. Philip H. Schwartz of the National Human Neural Stem Cell Resource at the Children s Hospital, Orange County Research Institute for providing hNSPC cultures.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Phase Contrast HemacytometerToolHausser Scientific02-671-54Distributed by Fisher under the indicated catalog #
Trypan Blue Stain 0.4%ReagentGIBCO, by Life Technologies15250-061Distributed by Invitrogen under the indicated catalog #

References

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  1. Marchenko, S., Flanagan, L. A. Passaging Human Neural Stem Cells. Journal of Visualized Experiments. 7, http://www.jove.com/index/Details.stp?ID=263 (2007).
  2. Caprette, D. avidR. Using a Hemacytometer. BioEd Online. ,

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Tags

Hemacytometer CountingTrypan Blue ExclusionCell Viability AssayHuman Neural Stem CellsCell Concentration CalculationDilution Factor MethodPhase Contrast MicroscopyLive Dead Cell DifferentiationCell Suspension PreparationQuadrant Cell Counting

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