Published August 2018 | Version Accepted Version + Supplemental Material
Journal Article Open

A catenin-dependent balance between N-cadherin and E-cadherin controls neuroectodermal cell fate choices

  • 1. ROR icon California State University, Northridge
  • 2. ROR icon California Institute of Technology

Abstract

Characterizing endogenous protein expression, interaction and function, this study identifies in vivo interactions and competitive balance between N-cadherin and E-cadherin in developing avian (Gallus gallus) neural and neural crest cells. Numerous cadherin proteins, including neural cadherin (Ncad) and epithelial cadherin (Ecad), are expressed in the developing neural plate as well as in neural crest cells as they delaminate from the newly closed neural tube. To clarify independent or coordinate function during development, we examined their expression in the cranial region. The results revealed surprising overlap and distinct localization of Ecad and Ncad in the neural tube. Using a proximity ligation assay and co-immunoprecipitation, we found that Ncad and Ecad formed heterotypic complexes in the developing neural tube, and that modulation of Ncad levels led to reciprocal gain or reduction of Ecad protein, which then alters ectodermal cell fate. Here, we demonstrate that the balance of Ecad and Ncad is dependent upon the availability of β-catenin proteins, and that alteration of either classical cadherin modifies the proportions of the neural crest and neuroectodermal cells that are specified.

Additional Information

© 2018 Published by Elsevier B.V. Received 12 April 2018, Revised 16 June 2018, Accepted 2 July 2018, Available online 14 July 2018. We would like to thank Dr. Mary-Pat Stein at CSUN and the Bronner lab at Caltech for helpful discussions, the CSUN biology department for funding and assistance, and the NIH NICHD for funding. Special thanks to Jackie Phillips and Karla Terrazas for their assistance with this project and for being super students and super women. No competing interests declared. Author contributions: Conceptualization, CDR and MEB; Methodology, CDR; Investigation, CDR and LKS; Validation and Formal Analysis, CDR; Writing –Original Draft, CDR; Writing –Review & Editing, CDR and MEB; Visualization, CDR; Funding Acquisition, CDR and MEB; Resources, CDR and MEB; Supervision, CDR and MEB. This work was supported by a National Institute of Health, NICHD P01 grant HD037105 to MEB, Startup Funding from CSUN to CDR, and a National Institute of Health, NICHD R15 grant R15HD092170 to CDR.

Attached Files

Accepted Version - nihms-1500927.pdf

Supplemental Material - 1-s2.0-S0925477318300819-mmc1.pdf

Supplemental Material - 1-s2.0-S0925477318300819-mmc2.docx

Files

1-s2.0-S0925477318300819-mmc1.pdf

Files (2.3 MB)

Name Size Download all
md5:f95bd949c9654c3fac0f30a8dbd68544
347.6 kB Preview Download
md5:9e68f3d30a7e980153f36f53eea7fdf3
16.8 kB Download
md5:75016b71be5ab3ae8b8c88acba6ca186
1.9 MB Preview Download

Additional details

Identifiers

PMCID
PMC6112866
Eprint ID
87944
DOI
10.1016/j.mod.2018.07.003
Resolver ID
CaltechAUTHORS:20180717-154246397

Related works

Funding

California State University, Northridge
NIH
HD037105
NIH
R15HD092170

Dates

Created
2018-07-17
Created from EPrint's datestamp field
Updated
2022-03-09
Created from EPrint's last_modified field