Regulation of cell protrusions by small GTPases during fusion of the neural folds

Author:

Rolo Ana1ORCID,Savery Dawn1,Escuin Sarah1,de Castro Sandra C1,Armer Hannah EJ2,Munro Peter MG2,Molè Matteo A1,Greene Nicholas DE1,Copp Andrew J1ORCID

Affiliation:

1. Newlife Birth Defects Research Centre, Institute of Child Health, University College London, London, United Kingdom

2. Imaging Unit, Institute of Ophthalmology, University College London, London, United Kingdom

Abstract

Epithelial fusion is a crucial process in embryonic development, and its failure underlies several clinically important birth defects. For example, failure of neural fold fusion during neurulation leads to open neural tube defects including spina bifida. Using mouse embryos, we show that cell protrusions emanating from the apposed neural fold tips, at the interface between the neuroepithelium and the surface ectoderm, are required for completion of neural tube closure. By genetically ablating the cytoskeletal regulators Rac1 or Cdc42 in the dorsal neuroepithelium, or in the surface ectoderm, we show that these protrusions originate from surface ectodermal cells and that Rac1 is necessary for the formation of membrane ruffles which typify late closure stages, whereas Cdc42 is required for the predominance of filopodia in early neurulation. This study provides evidence for the essential role and molecular regulation of membrane protrusions prior to fusion of a key organ primordium in mammalian development.

Funder

Wellcome Trust

Medical Research Council

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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