Summary

De células enteras de grabación de calcio activados por calcio de lanzamiento (CRAC) Las corrientes en los linfocitos T humanos

Published: December 21, 2010
doi:

Summary

Ofrecemos un protocolo de paso a paso para la grabación de células enteras patch clamp de calcio activados por calcio de lanzamiento (CRAC) las corrientes en mononucleares de sangre periférica de células derivadas de los linfocitos T humanos.

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. Preparación de los linfocitos T en reposo Humanos Utilizando RosetteSep Humanos Cocktail de enriquecimiento de células T y de densidad media RosetteSep, purificar las células T de muestras de sangre humana de acuerdo a las instrucciones del fabricante. La población de células resultante debe contener un 95% CD3 + células T en reposo. Purificamos linfocitos T humanos de sangre periférica recogida de voluntarios sanos, de acuerdo con el protocolo aprobado por el Consejo de la Universidad de…

Discussion

La investigación electrofisiológica de las corrientes de CRAC en reposo las células T humanas es una tarea difícil debido a la amplitud endógeno CRAC actual en estas células es pequeño debido al tamaño de células pequeñas (el diámetro de descanso de células T humanas está en el rango de 5.8 micras). Aquí se presenta un procedimiento paso a paso para registrar de forma fiable las corrientes CRAC en el descanso los linfocitos T humanos aislados a partir de células mononucleares de sangre periférica. Esta t…

Declarações

The authors have nothing to disclose.

Acknowledgements

Estamos agradecidos con el Departamento de Fisiología y Biología de Membrana de la Universidad de California Davis para que nos proporciona las instalaciones y un excelente ambiente para los estudios de los canales iónicos.

Materials

Material Name Tipo 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  

Referências

  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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Citar este artigo
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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