FIGURE

Fig. 4

ID
ZDB-FIG-170508-18
Publication
Sahu et al., 2017 - Calcium signals drive cell shape changes during zebrafish midbrain-hindbrain boundary formation
Other Figures
All Figure Page
Back to All Figure Page
Fig. 4

Calcium inhibition rescues NMII overactivation at the MHBC. (A) Hypothesized role of Ca2+ and NMII interactions. IF, inhibition of Ca2+ by 2-APB results in longer MHBC cells; AND, mypt1 knockdown results in overactivation of MRLC, causing shorter and wider MHB cells; THEN, inhibition of Ca2+ in mypt1-knockdown embryos would rescue MHBC cell length. (B, C) Confocal images of 24-ss embryos coinjected with mGFP and mypt1 MO and treated with (B) DMSO or (C) 2-APB. (B′, C′) Magnified images from B and C. Arrowheads indicate MHBC. (D, E) Cell length quantification at the MHBC and 40 μm outside the MHBC. For statistical analysis, the Mann–Whitney U test was done. **p < 0.01, mean ± SEM. For each measurement, mypt1 MO plus DMSO (n = 11; 22 cells) and mypt1 MO plus 2-APB (n = 13; 26 cells). Scale bars, 25 μm.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data
Fish:
Condition:
Knockdown Reagent:
Observed In:
Stage: 20-25 somites

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Mol. Biol. Cell