Figure 4.
Figure 4. CK2β is essential for microtubule architecture and tubulin polymerization as well as EB3 binding to polymerized tubulin. (A) Representative immunofluorescence confocal microscopy images of cultured fetal liver–derived ck2βfl/fl and ck2β−/− MKs. α-Tubulin staining appears fragmented in Ck2β−/− MKs undergoing proplatelet formation. Bar represents 20 μm (overview) and 5 μm (detail). (B) Representative immunoblots of 3 independent experiments of free and polymerized tubulin in ck2βfl/fl and ck2β−/− platelets (n = 3) in the absence and presence of paclitaxel (10 μM) in supernatant (sn) and pellet (p). (C) Representative immunoblots of EB3 bound to polymerized tubulin in ck2βfl/fl and ck2β−/− platelets (n = 3) after treatment with paclitaxel (10 μM) in supernatant (sn) and pellet (p).

CK2β is essential for microtubule architecture and tubulin polymerization as well as EB3 binding to polymerized tubulin. (A) Representative immunofluorescence confocal microscopy images of cultured fetal liver–derived ck2βfl/fl and ck2β−/− MKs. α-Tubulin staining appears fragmented in Ck2β−/− MKs undergoing proplatelet formation. Bar represents 20 μm (overview) and 5 μm (detail). (B) Representative immunoblots of 3 independent experiments of free and polymerized tubulin in ck2βfl/fl and ck2β−/− platelets (n = 3) in the absence and presence of paclitaxel (10 μM) in supernatant (sn) and pellet (p). (C) Representative immunoblots of EB3 bound to polymerized tubulin in ck2βfl/fl and ck2β−/− platelets (n = 3) after treatment with paclitaxel (10 μM) in supernatant (sn) and pellet (p).

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