Summary

Measuring Calpain Activity in Fixed and Living Cells by Flow Cytometry

Published: July 08, 2010
doi:

Summary

This article will detail the protocol for measuring calpain activity in fixed and living cells using flow cytometry.

Abstract

Calpains are ubiquitous intracellular, calcium-sensitive, neutral cysteine proteases 1. Calpains play crucial roles in many physiological processes, including signaling, cytoskeletal remodeling, regulation of gene expression, apoptosis and cell cycle progression 1. Calpains have been implicated in many pathologies including muscular dystrophies, cancer, diabetes, Alzheimer’s disease and multiple sclerosis 1. Calpain regulation is complex and incompletely understood. mRNA and protein levels correlate poorly with activity, limiting the use of gene or protein expression techniques to measure calpain activity. This video protocol details a flow cytometric assay developed in our laboratory for measuring calpain activity in fixed and living cells. This method uses the fluorescent substrate BOC-LM-CMAC, which is cleaved specifically by calpain, to measure calpain activity. 2 In this video, calpain activity in fixed and living murine 32Dkit leukemia cells, alone or as part of a splenocyte population is measured using an LSRII (BD Bioscience). 32Dkit cells are shown to have elevated activity compared to normal splenocytes.

Protocol

Prepare Reagents Note: All PBS contains Ca2+ and Mg2+ Detection Reagent Add 20μM 7-amino-4-chloromethyl coumarin, t-BOC-Leucine-methionine amide (BOC-LM-CMAC) to room temperature PBS. Each cell suspension will require 2mL detection reagent. 1% Paraformaldehyde (Fixed Cells) Dilute 4% paraformaldehyde stock solution in room temperature PBS. Aliquot 1mL 1% paraformaldehyde to each FACS tube. Three FACS t…

Discussion

The calpain activity in fixed and living 32Dkit cells has been determined in this video protocol. Treatment of the cell line with the calpain inhibitor PD150606 resulted in complete inhibition of calpain activity in the cells. In addition, treatment with the MEK1 inhibitor PD98059 resulted in complete inhibition of calpain activity in the cells. ERK is a major activator of calpain-2 3. These results suggest that calpain-2 activity is predominant in the 32Dkit cells. Current work in our laboratory is investigat…

Disclosures

The authors have nothing to disclose.

Acknowledgements

Supported by grants from the Canadian Institutes of Health Research, The Leukemia and Lymphoma Society of Canada and the Lymphoma Foundation of Canada.

Materials

Material Name Type Company Catalogue Number Comment
PBS
BOC-LM-CMAC 4%
paraformaldehyde
  Invitrogen  

Dissolve 4g paraformaldehyde in 100mL PBS. In fume hood, heat sample with stirring until clear.
Let cool then store at 4°C
PD150606   Invitrogen   Use freshly reconstituted PD150606 for maximal calpain inhibition.
PD98059   Cell Signaling Technology    
AlignFlow, AlignFlow plus fluorescent beads
FACS tubes
  Invitrogen    
LSR II   BD Bioscience  
Supernatant of WEHI-3 cells is used as a source of IL-3 in these experiments. Each collection of WEHI-3 supernatant is titrated to determine the optimal concentration used for 32Dkit cell growth.

References

  1. Goll, D. E., Thompson, V. F., Li, H., Wei, W., Cong, J. . The Calpain System. Physiol. Rev. 83, 731-801 (2003).
  2. Niapour, M., Berger, S. A. Flow Cytometric Measurement of Calpain Activity in Living Cells. Cytometry A. 71A, 475-485 (2007).
  3. Leloup, L., Daury, L., Mazéres, G., Cottin, P. Involvement of the ERK/MAP kinase signalling pathway in milli-calpain activation and myogenic cell migration. The International Journal of Biochemistry and Cell Biology. 39, 1177-1189 (2007).
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Cite This Article
Farr, C., Berger, S. Measuring Calpain Activity in Fixed and Living Cells by Flow Cytometry. J. Vis. Exp. (41), e2050, doi:10.3791/2050 (2010).

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