Mesenchymal Wnts are required for morphogenetic movements of calvarial osteoblasts during apical expansion

Author:

Polsani Nikaya1ORCID,Yung Theodora2ORCID,Thomas Evan2,Phung-Rojas Melissa1ORCID,Gupta Isha1,Denker Julie1,Lau Kimberly2,Feng Xiaotian1ORCID,Ibarra Beatriz1ORCID,Hopyan Sevan23ORCID,Atit Radhika P.145ORCID

Affiliation:

1. Research Institute, Case Western Reserve University 1 Department of Biology , , Cleveland, OH 44106 , USA

2. Research Institute, The Hospital for Sick Children 2 Program in Developmental and Stem Cell Biology , , Toronto, ON M5G 0A4 , Canada

3. The Hospital for Sick Children and Departments of Molecular Genetics and Surgery, University of Toronto 3 Division of Orthopedics , , Toronto, ON M5G 1X8 , Canada

4. Research Institute, Case Western Reserve University 4 Department of Dermatology , , Cleveland, OH 44106 , USA

5. Research Institute, Case Western Reserve University 5 Department of Genetics and Genome Sciences , , Cleveland, OH 44106 , USA

Abstract

ABSTRACT Apical expansion of calvarial osteoblast progenitors from the cranial mesenchyme (CM) above the eye is integral to calvarial growth and enclosure of the brain. The cellular behaviors and signals underlying the morphogenetic process of calvarial expansion are unknown. Time-lapse light-sheet imaging of mouse embryos revealed calvarial progenitors intercalate in 3D in the CM above the eye, and exhibit protrusive and crawling activity more apically. CM cells express non-canonical Wnt/planar cell polarity (PCP) core components and calvarial osteoblasts are bidirectionally polarized. We found non-canonical ligand Wnt5a−/− mutants have less dynamic cell rearrangements and protrusive activity. Loss of CM-restricted Wntless (CM-Wls), a gene required for secretion of all Wnt ligands, led to diminished apical expansion of Osx+ calvarial osteoblasts in the frontal bone primordia in a non-cell autonomous manner without perturbing proliferation or survival. Calvarial osteoblast polarization, progressive cell elongation and enrichment for actin along the baso-apical axis were dependent on CM-Wnts. Thus, CM-Wnts regulate cellular behaviors during calvarial morphogenesis for efficient apical expansion of calvarial osteoblasts. These findings also offer potential insights into the etiologies of calvarial dysplasias.

Funder

National Institute of Dental and Craniofacial Research

National Institutes of Health

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Canadian Institutes of Health Research

Canada First Research Excellence Fund

Medicine by Design

Publisher

The Company of Biologists

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