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. Author manuscript; available in PMC: 2013 May 11.
Published in final edited form as: Biochem Biophys Res Commun. 2012 Apr 19;421(3):605–611. doi: 10.1016/j.bbrc.2012.04.054

Table I. Rates of forward and reverse translocation of γ subunit types on activation of endogenous receptors in HeLa cells.

t1/2 values are in seconds. F - forward translocation. Increase in intracellular membrane FP-γ subunit fluorescence intensity on agonist activation was plotted and t1/2 determined. R- reverse translocation. Decrease in intracellular membrane FP-γ subunit fluorescence intensity on antagonist addition was plotted and t1/2 determined. CXCR4 receptors were activated with 100 ng/ml SDF-1α and deactivated with 20 µM AMD 3100. α2-AR receptors were activated with 10 µM norepinephrine and deactivated with 60 µM yohimbine.

CXCR4 α2-AR CXCR4 α2-AR CXCR4 α2-AR
γ9-F
γ9-R
10±2(10)
19±2
14±2(7)
19±4
γ5-F
γ5-R
66±5(5)
167±
65±3(9)
127±8
γ8-F
γ8-R
123±5(6)
111±3
N.D.
N.D.
γ1-F
γ1-R
20±1(6)
22±1
N.D.
N.D.
γ12-F
γ12-R
89±2(6)
104±4
61±3(10)
87±11
γ4-F
γ4-R
118±6(7)
143±19
N.D.
N.D.
γ11F
γ11-R
36±3(7)
65±9
15±3(4)
28±1
γ10-F
γ10-R
95±3(8)
95±3
48±5(7)
60±9
γ2-F
γ2-R
161±13(6)
145±5
191±25(6)
N.D.
γ7-F
γ7-R
45±1(5)
74±3
58±12(6)
100±27
γ13-F
γ13-R
100±2(7)
212±2
56±7(6)
53±3
γ3-F
γ3-R
286±17(10)
296±9
219±61(6)
N.D.

Mean ± SEM (no. of cells).

N.D. - not done. Cells were from multiple dishes.