Summary

Whole-Cell Recording of Calcium Release-Activated Calcium (CRAC) Currents in Human T Lymphocytes

Published: December 21, 2010
doi:

Summary

We provide a step-by-step protocol for whole-cell patch clamp recording of Calcium Release-Activated Calcium (CRAC) currents in peripheral blood mononuclear cell-derived human T lymphocytes.

Abstract

In T lymphocytes, depletion of Ca2+ from the intracellular Ca2+ store leads to activation of plasmalemmal Ca2+ channels, called Calcium Release-Activated Calcium (CRAC) channels. CRAC channels play important role in regulation of T cell proliferation and gene expression. Abnormal CRAC channel function in T cells has been linked to severe combined immunodeficiency and autoimmune diseases 1, 2 . Studying CRAC channel function in human T cells may uncover new molecular mechanisms regulating normal immune responses and unravel the causes of related human diseases. Electrophysiological recordings of membrane currents provide the most accurate assessment of functional channel properties and their regulation. Electrophysiological assessment of CRAC channel currents in Jurkat T cells, a human leukemia T cell line, was first performed more than 20 years ago 3, however, CRAC current measurements in normal human T cells remains a challenging task. The difficulties in recording CRAC channel currents in normal T cells are compounded by the fact that blood-derived T lymphocytes are much smaller in size than Jurkat T cells and, therefore, the endogenous whole-cell CRAC currents are very low in amplitude. Here, we give a step-by-step procedure that we routinely use to record the Ca2+ or Na+ currents via CRAC channels in resting human T cells isolated from the peripheral blood of healthy volunteers. The method described here was adopted from the procedures used for recording the CRAC currents in Jurkat T cells and activated human T cells 4-8.

Protocol

1. Preparation of Resting Human T Lymphocytes Using RosetteSep Human T Cell Enrichment Cocktail and RosetteSep Density Medium, purify T cells from human blood samples according to the manufacturer’s instructions. The resulting cell population should contain 95% CD3+ resting T cells. We purify human T lymphocytes from peripheral blood samples collected from healthy volunteers in accordance with the protocol approved by the UC Davis Internal Review Board. After isolation, resuspe…

Discussion

The electrophysiological investigation of CRAC currents in resting human T cells is a challenging task because the endogenous CRAC current amplitude in these cells is small due to the small cell size (the resting human T cell diameter is in the range of 5-8 μm). Here, we present a step-by-step procedure to reliably record CRAC currents in resting human T lymphocytes isolated from peripheral blood mononuclear cells. This technology allows us to investigate the physiology and functional expression of CRAC channels in re…

Disclosures

The authors have nothing to disclose.

Acknowledgements

We are thankful to the Department of Physiology and Membrane Biology, University of California Davis for providing us with facilities and an excellent environment for the studies of ion channels.

Materials

Material Name Type Company Catalogue Number Comment
RosetteSep Human T Cell Enrichment Cocktail   StemCell Technologies, Vancouver, BC, Canada 15061  
RosetteSep Density Medium   StemCell Technologies 15705  
RPMI-in 1640 medium w/glutamine/HEPES   Fisher, Waltham, MA SH3025501  
Fetal Calf Serum   Omega Scientific, Tarzana, CA FB-01  
GlutaMAX-I (100X solution)   Invitrogen, Carlsbad, CA 35050  
RPMI 1640 vitamin solution (100X)   Sigma-Aldrich 7256  
1640 amino acids solution (50X)   Sigma-Aldrich R7131  
Sodium pyruvate   Sigma-Aldrich S8636  
β-Mercaptoethanol   Sigma-Aldrich M7522  
Inositol trisphosphate   Sigma-Aldrich 19766  
BAPTA   Sigma-Aldrich A4926  
Poly-L-Lysine Hydrobromide   Sigma-Aldrich P2636  
Lanthanum Chloride   Sigma-Aldrich 262072  
Thapsigargin   Calbiochem 586005  
Sylgard 184 Silicon Elastomer Kit   Dow Corning, Midland, MI 3097358-1004  
HIPEC R6101 Semiconductor Protective Coating   Dow Corning, Midland, MI    
63-500 Series High-Performance Vibration Isolation Lab Table   Technical Manufacturing, Peabody, MA 63-540  
EPC 10 patch clamp amplifier with headstage   HEKA Instruments, Bellmore, NY    
Micromanipulator   Sutter Instrument, Novato, CA MP-285  
Olympus 1X71 Inverted microscope with 40x oil immersion objective   Olympus America, Center Valley, PA 1X71  
Windows Computer   Dell    
Pulse software   HEKA Instruments    
Origin Scientific Graphing and Analysis Software   OriginLab, Northampton, MA    
Patch pipette puller   Sutter Instrument P-97  
Borosilicate glass with filament (O.D.: 1.5mm and I.D.: 1.10mm   Sutter Instrument BF150-110-7.5  
Narashige’s Microforge   Tritech Research, Los Angeles, CA MF-830  
Silicon O-rings   McMASTER-CARR, Santa Fe Springs, CA 111 S70  
Coverslips 25 mm   Fisher Scientific 12-545-102 25 mm 25CIR.-1  

References

  1. Parekh, A. B. Store-operated CRAC channels: function in health and disease. Nat Rev Drug Discov. 9, 399-410 (2010).
  2. Feske, S. CRAC channelopathies. Pflugers Arch. , (2010).
  3. Lewis, R. S., Cahalan, . Mitogen-induced oscillations of cytosolic Ca2+ and transmembrane Ca2+ current in human leukemic T cells. Cell Regul. 1, 99-112 (1989).
  4. Zweifach, A., Lewis, R. S. Rapid inactivation of depletion-activated calcium current (ICRAC) due to local calcium feedback. J Gen Physiol. 105, 209-226 (1995).
  5. Zweifach, A., Lewis, R. S. Slow calcium-dependent inactivation of depletion-activated calcium current. Store-dependent and -independent mechanisms. J Biol Chem. 270, 14445-1451 (1995).
  6. Zweifach, A., Lewis, R. S. Calcium-dependent potentiation of store-operated calcium channels in T lymphocytes. J Gen Physiol. 107, 597-610 (1996).
  7. Prakriya, M., Lewis, R. S. Separation and characterization of currents through store-operated CRAC channels and Mg2+-inhibited cation (MIC) channels. J Gen Physiol. 119, 487-507 (2002).
  8. Fomina, A. F., Fanger, C. M., Kozak, J. A., Cahalan, . Single channel properties and regulated expression of Ca(2+) release-activated Ca(2+) (CRAC) channels in human T cells. J Cell Biol. 150, 1435-1444 (2000).
  9. Sakmann, B., Neher, E. . Single-Channel Recording. , (1995).
  10. Neher, E. Correction for liquid junction potentials in patch clamp experiments. Methods Enzymol. 207, 123-1231 (1992).
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Cite This Article
Thakur, P., Fomina, A. F. Whole-Cell Recording of Calcium Release-Activated Calcium (CRAC) Currents in Human T Lymphocytes. J. Vis. Exp. (46), e2346, doi:10.3791/2346 (2010).

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