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Fig. 9. foxi1-HGR induces ae1 and alpha-INCs. (A-D) Embryos were injected at the 2-cell stage with foxi1-HGR, treated with DEX at stage 12 and then processed for ae1 and pendrin expression by whole-mount in situ hybridization. Shown are representative examples of uninjected and injected regions. Note that foxi1-HGR induces a massive increase in ae1 expression, but only a small increase in the number of cells expressing pendrin. (E,F) Example of a control transplant (E) stained with antibody to ae1 (F). (H,I) Example of a transplant onto a host injected with foxi1-HGR RNA (H) and stained with ae1 antibodies. The arrowhead marks ae1-negative INC (I). (G) Transplant assay where the outer layer is removed from ectoderm at stage 10 from a mGFP-injected host and placed on the inner layer of a host injected with mRFP or with both foxi1-HGR and mRFP RNA. INCP, intercalating non-ciliated cell precursor; CCP, ciliated cell precursor. (J) Quantification of ae1-positive and -negative INCs in control or foxi1-HGR injected hosts (three random fields from at least eight embryos per condition). Error bars indicate ± s.d. All values between a given INC subtype under the various conditions are significantly different relative to the control, based on a two-tailed t-test (P≤0.005). Scale bar: 20 µm.

Image published in: Quigley IK et al. (2011)

Copyright © 2011. 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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