Figure 1. Differential activity of NMII isoforms. (A) Representative fluorescence recovery kinetics of NMIIA and NMIIB in CD41a+CD42+ megakaryocytes (MK) on day 7 of in vitro culture. (B) Western blot analysis of the expression of NMIIA and NMIIB in Triton X-100 fractionation-based supernatant (S) and pellet (P) fractions of in vitro cultured day 7 control megakaryocytes and megakaryocytes treated with Y27632 for 24 hours. Densitometric analysis is provided in supplemental Figure 2. (C) Representative fluorescence recovery kinetics of NMIIA-GFP and NMIIB-GFP in erythroblasts (ERY) on day 8 of culture. (D) Fluorescence recovery kinetics of NMIIA and NMIIB in CD41a+CD42+ megakaryocytes on day 7 of culture pretreated with Y27632 (ROCK inhibitor) for 24 hours. (E) Fluorescence recovery kinetics of NMIIA-GFP and NMIIB-GFP in erythroblasts on day 9 of culture after incubation in the presence of 10 μM Y27632 for 24 hours.
Figure 1.

Differential activity of NMII isoforms. (A) Representative fluorescence recovery kinetics of NMIIA and NMIIB in CD41a+CD42+ megakaryocytes (MK) on day 7 of in vitro culture. (B) Western blot analysis of the expression of NMIIA and NMIIB in Triton X-100 fractionation-based supernatant (S) and pellet (P) fractions of in vitro cultured day 7 control megakaryocytes and megakaryocytes treated with Y27632 for 24 hours. Densitometric analysis is provided in supplemental Figure 2. (C) Representative fluorescence recovery kinetics of NMIIA-GFP and NMIIB-GFP in erythroblasts (ERY) on day 8 of culture. (D) Fluorescence recovery kinetics of NMIIA and NMIIB in CD41a+CD42+ megakaryocytes on day 7 of culture pretreated with Y27632 (ROCK inhibitor) for 24 hours. (E) Fluorescence recovery kinetics of NMIIA-GFP and NMIIB-GFP in erythroblasts on day 9 of culture after incubation in the presence of 10 μM Y27632 for 24 hours.

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