Figure 3
Figure 3. Effects of PGE1 on platelet activation and fibrin formation. Platelets were superfused with plasma at 250 s−1 in the absence (control) or presence (0.5μM) of PGE1. Bright-field and contrast images (Nikon Diaphot 200 microscope, see “Methods”) were taken at 0-60 seconds after start of fibrin formation (bars, 10 μm). (A) Reduced fibrin on platelets after PGE1 treatment (average pixel intensities of subtracted images). (B) Lower [Ca2+]i rises with PGE1 in Fluo-4–loaded platelets. (C) Lower OG488–annexin A5 staining with PGE1. (D) Reduced OG488-fibrin(ogen) staining (integrated fluorescent intensities). Means ± SE; n ≥ 3; *P < .05, ***P < .001 vs control.

Effects of PGE1 on platelet activation and fibrin formation. Platelets were superfused with plasma at 250 s−1 in the absence (control) or presence (0.5μM) of PGE1. Bright-field and contrast images (Nikon Diaphot 200 microscope, see “Methods”) were taken at 0-60 seconds after start of fibrin formation (bars, 10 μm). (A) Reduced fibrin on platelets after PGE1 treatment (average pixel intensities of subtracted images). (B) Lower [Ca2+]i rises with PGE1 in Fluo-4–loaded platelets. (C) Lower OG488–annexin A5 staining with PGE1. (D) Reduced OG488-fibrin(ogen) staining (integrated fluorescent intensities). Means ± SE; n ≥ 3; *P < .05, ***P < .001 vs control.

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