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. 2018 Dec 19;294(10):3464–3475. doi: 10.1074/jbc.RA118.006535

Table 2.

Affinities for binding of C-C motif chemokines to CCR1

Binding was determined using a radioligand (125I-CCL3) displacement assay with membranes prepared from cells grown in the absence of chlorate or the presence of 30 mm chlorate to inhibit sulfation for 48 h prior to membrane preparation. CCR1 expression was induced by the addition of 10 μg/ml tetracycline to the cell medium 24 h prior to membrane preparation. Inhibition constants are reported as pIC50 values (−log10 of the IC50; in m) ± S.E. The corresponding IC50 values (in nm) are shown in parentheses. CCL7 was used as a reference for statistical analysis. *, p < 0.05; ***, p < 0.001.

Chemokine pIC50 (no chlorate treatment) pIC50 (chlorate-treated cells)
m m
CCL2 7.2 ± 0.1 (57.5)*** 7.7 ± 0.1 (19.1)***
CCL5 9.2 ± 0.2 (0.6) 9.7 ± 0.1 (0.2)
CCL7 9.6 ± 0.1 (0.4) 9.8 ± 0.1(0.2)
CCL8 8.7 ± 0.2 (1.8)* 8.7 ± 0.1 (1.9)***
CCL15 10.1 ± 0.2 (0.07) 10.0 ± 0.1 (0.1)
CCL26 No binding 6.3 ± 0.2 (457.1)***