Glypican 4 mediates Wnt transport between germ layers via signaling filopodia
Abstract
Glypicans influence signaling pathways by regulating morphogen trafficking and reception. However, the underlying mechanisms in vertebrates are poorly understood. In zebrafish, Glypican 4 (Gpc4) is required for convergence and extension (C&E) of both the mesoderm and endoderm. Here, we show that transgenic expression of GFP-Gpc4 in the endoderm of gpc4 mutants rescued C&E defects in all germ layers. The rescue of mesoderm was likely mediated by Wnt5b and Wnt11f2 and depended on signaling filopodia rather than on cleavage of the Gpc4 GPI anchor. Gpc4 bound both Wnt5b and Wnt11f2 and regulated formation of the filopodia that transport Wnt5b and Wnt11f2 to neighboring cells. Moreover, this rescue was suppressed by blocking signaling filopodia that extend from endodermal cells. Thus, GFP-Gpc4–labeled protrusions that emanated from endodermal cells transported Wnt5b and Wnt11f2 to other germ layers, rescuing the C&E defects caused by a gpc4 deficiency. Our study reveals a new mechanism that could explain in vivo morphogen distribution involving Gpc4.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Sep 30, 2021
- Source ID
- 10.1083/jcb.202009082
Entities
People
- Anurag Kakkerla Balaraju
- Bo Hu
- Fang Lin
- Heston Steen
- Juan J. Rodriguez
- Nhan T. Nguyen
- Saeb Suhaib
- Songhai Chen
- Yuanyuan Gao
Organizations
- National Institutes of Health
- National Science Foundation
- United States Department of Defense
- University of Iowa