Cadherin2/4-signaling via PTP1B and catenins is critical for nucleokinesis during radial neuronal migration in the neocortex

Author:

Martinez-Garay Isabel12,Gil-Sanz Cristina1,Franco Santos J34,Espinosa Ana1,Molnár Zoltán5,Mueller Ulrich1ORCID

Affiliation:

1. Molecular and Cellular Neuroscience Department, Dorris Neuroscience Center, The Scripps Research Institute, La Jolla, CA 92037, USA

2. Present address: Division of Neuroscience, School of Biosciences, Cardiff University, Cardiff CF10 3AX, UK

3. Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA

4. Program of Pediatric Stem Cell Biology, Children's Hospital Colorado, Aurora, CO 80045, USA

5. Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, OX1 3QX, United Kingdom

Abstract

Cadherins are critical for the radial migration of excitatory projection neurons into the developing neocortical wall. However, the specific cadherins and the signaling pathways that regulate radial migration are not well understood. Here we show that cadherin 2 (CDH2) and CDH4 cooperate to regulate radial migration via the protein tyrosine phosphatase 1B (PTP1B) and α- and β-catenins. Surprisingly, perturbation of cadherin-mediated signaling does not affect the formation and extension of leading processes of migrating neocortical neurons. Instead, movement of the cell body and nucleus (nucleokinesis) is disrupted. This defect is partially rescued by overexpression of LIS1, a microtubule associated protein that has previously been shown to regulate nucleokinesis. Taken together our findings indicate that cadherin-mediated signaling to the cytoskeleton is critical for nucleokinesis of neocortical projection neurons during their radial migration.

Funder

National Institute of Health

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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