Fig. 1. PKD is expressed in human platelets and is activated by PMA, convulxin, thrombin, and U46619. / Washed platelets were treated with indomethacin (10 μM) and apyrase (2 U/mL), with the exception of those activated by U46619, which were treated with apyrase alone. (A) Whole cell lysates from platelets (12.5 × 106 cells) and Jurkat T cells (12.5 × 105 cells) were subjected to SDS-PAGE, transferred to PVDF membrane, immunoblotted with PA-1 antiserum, and visualized by chemiluminescence. Similar results were obtained using 2 other anti-PKD antibodies, sc639 and sc937 (data not shown). One experiment representative of 3 is shown. (B) Time courses of PKD activation were obtained using PMA (30 nM), convulxin (12 nM), thrombin (0.1 U/mL), and U46619 (3 μM). (i) Platelets were lysed and immunoprecipitated with the sc937 antiserum and PKD activity was determined by an in vitro kinase assay using peptide syntide-2 as substrate. Results are shown as the mean ± SEM and are representative of 3 independent experiments, each in duplicate. (ii) Lysates were analyzed by SDS-PAGE and Western blotting with the pS916 antibody, and the Western blots were reprobed with a pan–C-terminal PKD antibody (pan sc639). One experiment representative of 3 independent experiments is shown.
Fig. 1.

PKD is expressed in human platelets and is activated by PMA, convulxin, thrombin, and U46619.

Washed platelets were treated with indomethacin (10 μM) and apyrase (2 U/mL), with the exception of those activated by U46619, which were treated with apyrase alone. (A) Whole cell lysates from platelets (12.5 × 106 cells) and Jurkat T cells (12.5 × 105 cells) were subjected to SDS-PAGE, transferred to PVDF membrane, immunoblotted with PA-1 antiserum, and visualized by chemiluminescence. Similar results were obtained using 2 other anti-PKD antibodies, sc639 and sc937 (data not shown). One experiment representative of 3 is shown. (B) Time courses of PKD activation were obtained using PMA (30 nM), convulxin (12 nM), thrombin (0.1 U/mL), and U46619 (3 μM). (i) Platelets were lysed and immunoprecipitated with the sc937 antiserum and PKD activity was determined by an in vitro kinase assay using peptide syntide-2 as substrate. Results are shown as the mean ± SEM and are representative of 3 independent experiments, each in duplicate. (ii) Lysates were analyzed by SDS-PAGE and Western blotting with the pS916 antibody, and the Western blots were reprobed with a pan–C-terminal PKD antibody (pan sc639). One experiment representative of 3 independent experiments is shown.

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