Figure 1
Figure 1. Orai1 is the platelet SOC channel. (A) RT-PCR and Western blot analysis of human platelets. Orai1, Orai2, and Orai3 were assessed with the primer pairs described in Takahashi et al,22 and Western blot was performed using an antibody from ProSci. (B) Wild-type and Orai1−/− littermates (3 weeks old). (C) Body weights of wild-type (+/+) and Orai1−/− (−/−) mice. Error bars represent plus or minus SD. (D) RT-PCR analyses of platelet and thymocyte mRNA from wild-type (+/+), original Orai1−/− (−/−), and Orai1−/− bone marrow chimera (−/− BMc) mice. Orai1-, Orai2-, and Orai3-specific forward and reverse primers were used22; actin served as control. (E) Fura-2–loaded platelets were stimulated with 5 μM TG for 10 minutes, followed by addition of 1 mM extracellular Ca2+ and monitoring of [Ca2+]i. Representative measurements (left) and maximal Δ[Ca2+]i plus or minus SD (n = 4 per group) before and after addition of 1 mM Ca2+ (right) are shown. □ represents Stim1−/− platelets.

Orai1 is the platelet SOC channel. (A) RT-PCR and Western blot analysis of human platelets. Orai1, Orai2, and Orai3 were assessed with the primer pairs described in Takahashi et al,22  and Western blot was performed using an antibody from ProSci. (B) Wild-type and Orai1−/− littermates (3 weeks old). (C) Body weights of wild-type (+/+) and Orai1−/− (−/−) mice. Error bars represent plus or minus SD. (D) RT-PCR analyses of platelet and thymocyte mRNA from wild-type (+/+), original Orai1−/− (−/−), and Orai1−/− bone marrow chimera (−/− BMc) mice. Orai1-, Orai2-, and Orai3-specific forward and reverse primers were used22 ; actin served as control. (E) Fura-2–loaded platelets were stimulated with 5 μM TG for 10 minutes, followed by addition of 1 mM extracellular Ca2+ and monitoring of [Ca2+]i. Representative measurements (left) and maximal Δ[Ca2+]i plus or minus SD (n = 4 per group) before and after addition of 1 mM Ca2+ (right) are shown. □ represents Stim1−/− platelets.

Close Modal

or Create an Account

Close Modal
Close Modal