XB-IMG-42385
Xenbase Image ID: 42385
Fig. 4. xMIDs regulate the localization of adhesive molecules. (A-H′) Transverse sections through the neural plate of unilaterally control-Mo-injected (Cont.-Mo) (A,C,E,G) and xMID-Mo-injected (B,D,F,H) Xenopus embryos at stage 15.5, stained with antibodies against ZO-1 (A,B), C-cadherin (C-cad.) (C,D), β-catenin (β-cat.) (E,F), or laminin (G,H). Flag-β-globin mRNA (250 pg) was co-injected as a tracer, and stained with an anti-Flag antibody (magenta). (A-F) Dashed lines indicate Flag-positive Mo-injected cells. (H) Arrowheads indicate the attenuation of laminin accumulation basal to the xMID-Mo-injected cells. (H′) Higher-magnification view of the boxed area in H. Scale bars: 50 μm. (I-L) Quantification of marker intensities in the morphants at stage 15.5. For ZO-1 intensity: control-Mo, n=27 sites (3 embryos); xMID-Mo, n=44 sites (6 embryos). For C-cadherin: control-Mo, n=16 sites (4 embryos); xMID-Mo, n=20 sites (5 embryos). For β-catenin: control-Mo, n=7 sites (3 embryos); xMID-Mo, n=15 sites (4 embryos). For laminin: control-Mo, n=19 sites (4 embryos); xMID-Mo, n=19 sites (3 embryos). *P<0.05, **P<0.001. (M,N) Schematic illustrations showing the control (M) and xMID (N) morphants. Rectangles indicate the regions analyzed in this study. so, somite; nt, notochord. Image published in: Suzuki M et al. (2010) Copyright © 2010. Image reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.
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