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Fig. 8. CysLT1 receptor expression and heterologous desensitization in COS-7 cells. Confocal microscopy of the CysLT1 receptor trafficking in intact COS-7 cells. (A) COS-7 cells expressing HA-tagged CysLT1 receptor were immunoprecipitated with HA monoclonal antibody and visualized with an CysLT1 polyclonal antibody. (B) Equilibrium mixed-type binding curve of [3H]LTD4 in membranes from COS-7 cells transiently transfected with HA-tagged CysLT1 receptor. Binding of [3H]LTD4 is expressed as the ratio of bound ligand concentration to total ligand concentration (B/T, dimensionless) versus the logarithm of total ligand concentration (Log T). Two independent [3H]LTD4 mixed-type experiments were performed, each with triplicate determinations, and analyzed simultaneously. For the sake of clarity, only one representative curve is shown; the curve is computer generated. (Inset) The percentage of total [3H]LTD4 binding and displacement by unlabeled LTD4, ATP or UDP. (C) Representative traces of the [Ca2+]i transient induced by 30 µM ATP (2nd challenge) before and after an initial challenge with 1 µM LTD4. (D) Representative traces of the [Ca2+]i transient induced by 1 µM LTD4 (2nd challenge) before and after an initial challenge with 30 µM of ATP. (E) Confocal laser scanning microscopy of the subcellular distribution of the CysLT1 receptors performed using a specific antibody raised against the C-terminal tail. Cells were fixed with paraformaldehyde and permeabilized with Triton X-100 in basal conditions (control) and after a 5 minute challenge with the indicated stimuli. Immunocytochemical staining of COS-7 cells after stimulation with vehicle (left), 1 µM LTD4 (middle), 30 µM ATP (right). The experiment shown is representative of two others performed.





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