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. 2011 Nov 1;5(6):510–517. doi: 10.4161/chan.5.6.18222

Table 1.

Maximal CRAC channel currents, CRAC channel densities, and morphometric parameters of resting, activated, and Jurkat T cells

T cell type Ca2+-ICRAC maximal amplitude at −100 mV (pA) Na+-ICRAC maximal amplitude at −100 mV (pA) Number of channels per cell* Cell surface area (µm2)** Channel surface density (channels/µm2) Cell diameters (µm)*** Cell volume (fL)****
Resting −5.3 ± 0.8 (n = 24) −26.1 ± 3.0 (n = 19) ∼1,400 198.6 ± 8.8 (n = 24) ∼7 6.4 ± 0.03 (n = 101) 137.2 ± 2.2 (n = 101)
Activated −7.6 ± 0.8 (n = 32) −52.0 ± 6.4 (n = 29) ∼2,000 741.1 ± 26.1 (n = 32) ∼2.7 11.8 ± 0.1 (n = 122) 894 ± 34.9 (n = 122)
Jurkat −12.5 ± 1.3 (n = 25) −62.4 ± 7.0 (n = 21) ∼3,300 744.2 ± 37.2 (n = 25) ∼4.4 12.3 ± 0.16 (n = 143) 1049.7 ± 38.3 (n = 143)

Average ± SE are presented; n is number of cells.

*

Calculated using an estimated value of unitary CRAC channel amplitude of 3.8 fA at −110 mV in 20 mM Ca2+ Ringer solution.36

**

Calculated from Cm values assuming the cell membrane specific capacitance of 0.01 pF µm−2.

***

Measured from transmitted light images as shown in Figure 2D.

****

Calculated from cell diameters measured in transmitted light images.