This proposal concerns signaling mechanisms regulating cell orientation in the epithelial plane in the vertebrate embryo that is known as planar cell polarity (PCP). This common phenomenon is mediated by a group of conserved proteins that polarize to one side of an epithelial cell in the tissue. Secreted Wnt proteins have been implicated in the control of PCP, but whether and how Wnt proteins provide the directional input to the PCP system remains unclear. Our laboratory has a long-term interest in Wnt signaling and cell polarity, but mechanistic studies were hampered by lack of tractable models and suitable molecular markers. Recently, our group has developed specific antibodies and fluorescent sensors for PCP analysis and discovered a unique polarity of cells in Xenopus gastrula epidermis and the neural plate. The proposed studies will use the new tools to address the following key questions that continue to challenge the field. A. What mechanisms are responsible for core PCP protein segregation in polarized cells? B. What are the spatial cues or signals that control PCP? C. How does cell polarization translate into morphogenetic cell behaviors? Our experiments will uncover molecular mechanisms regulating polarization of the core PCP protein Vangl2 to the anterior apical edge of cells in the Xenopus. Other studies will clarify the role of Wnt ligands in this process and identify new proteins that function in PCP using mass spectrometry-based approaches. These experiments will use Xenopus embryos, a unique in vivo model, in which biochemical, embryological and cell biological approaches can be combined. The proposed studies will advance the knowledge of basic cell biological mechanisms underlying vertebrate early morphogenetic events, such as gastrulation and neurulation. Since misregulation of Wnt and PCP signaling has been causally linked to many congenital defects and syndromes, polycystic kidney disease and multiple cancers, these studies are highly relevant to human health.

Public Health Relevance

This application focuses on signaling mechanisms triggered by secreted Wnt proteins and regulating cell polarity and cell movements during vertebrate embryonic development. The proposed studies will contribute to the knowledge necessary for prevention of birth abnormalities and are relevant to metastatic cancers and other diseases linked to alterations of cell polarity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
1R35GM122492-01
Application #
9275763
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Hoodbhoy, Tanya
Project Start
2017-08-01
Project End
2022-07-31
Budget Start
2017-08-01
Budget End
2018-07-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
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Ossipova, Olga; Kerney, Ryan; Saint-Jeannet, Jean-Pierre et al. (2018) Regulation of neural crest development by the formin family protein Daam1. Genesis 56:e23108
Chuykin, Ilya; Ossipova, Olga; Sokol, Sergei Y (2018) Par3 interacts with Prickle3 to generate apical PCP complexes in the vertebrate neural plate. Elife 7: