Figure 2.
Cyfip1-deficient platelets are unable to form lamellipodia on a fibrinogen-coated surface. (A) Washed platelets were allowed to spread on fibrinogen, following fixation at the indicated time points (n = 3, representative for 3 independent experiments). Scale bar, 5 µm. (B) Quantification of the different spreading phases of fixed platelets after 5, 15, and 30 minutes from differential interference contrast images (Zeiss Axiovert 200 inverted microscope [100×/1.4 oil objective]). (C) Phase abundance of live cells over time (wild type [WT], n = 58; knockout [KO], n = 32). Quantification of (D) platelet size and (E) platelet perimeter (WT, n = 100; KO, n = 58) of all Cyfip1+/+ and Cyfip1−/− platelets present in a visual field after 30-minute spreading. (F) Length and (G) number of filopodia (WT, n = 58; KO, n = 32) of live platelets in phase 2 spreading. Values are mean plus or minus SD. ***P < .001.

Cyfip1-deficient platelets are unable to form lamellipodia on a fibrinogen-coated surface. (A) Washed platelets were allowed to spread on fibrinogen, following fixation at the indicated time points (n = 3, representative for 3 independent experiments). Scale bar, 5 µm. (B) Quantification of the different spreading phases of fixed platelets after 5, 15, and 30 minutes from differential interference contrast images (Zeiss Axiovert 200 inverted microscope [100×/1.4 oil objective]). (C) Phase abundance of live cells over time (wild type [WT], n = 58; knockout [KO], n = 32). Quantification of (D) platelet size and (E) platelet perimeter (WT, n = 100; KO, n = 58) of all Cyfip1+/+ and Cyfip1−/− platelets present in a visual field after 30-minute spreading. (F) Length and (G) number of filopodia (WT, n = 58; KO, n = 32) of live platelets in phase 2 spreading. Values are mean plus or minus SD. ***P < .001.

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