Journal article
Glypican 4 and Mmp14 interact in regulating the migration of anterior endodermal cells by limiting extracellular matrix deposition
Development (Cambridge), Vol.145(17), p.dev163303
08/06/2018
DOI: 10.1242/dev.163303
PMID: 30082271
Abstract
During embryogenesis the germ layers, including the endoderm, undergo convergence and extension (C&E) movements to narrow and elongate the body plan. In zebrafish, the dorsal migration of endodermal cells during gastrulation is controlled by chemokine signaling, but little is known about how they migrate during segmentation. Here we show that Glypican4 (Gpc4), a member of the heparin sulphate proteoglycan family, is required for efficient migration of anterior endodermal cells during early segmentation, regulating Rac activation to maintain polarized actin-rich lamellipodia. An endoderm transplantation assay showed that Gpc4 regulates endoderm migration in a non-cell-autonomous fashion. Further analyses revealed that the impaired endoderm migration in
mutants results from increases in the expression and assembly of fibronectin and laminin, major components of the extracellular matrix (ECM). Notably, we found that the matrix metalloproteinase 14 (Mmp14a/b) are required for the control of ECM expression during endoderm migration, with Gpc4 acting through Mmp14a/b to limit ECM expression. Our results suggest that Gpc4 is critical for generating the environment required for efficient migration of endodermal cells, uncovering a novel function of Gpc4 during development.
Details
- Title: Subtitle
- Glypican 4 and Mmp14 interact in regulating the migration of anterior endodermal cells by limiting extracellular matrix deposition
- Creators
- Bo Hu - Department of Anatomy and Cell Biology, Carver College of Medicine, the University of Iowa, Iowa City, IA 52242, USAYuanyuan Gao - Department of Anatomy and Cell Biology, Carver College of Medicine, the University of Iowa, Iowa City, IA 52242, USALauren Davies - Department of Anatomy and Cell Biology, Carver College of Medicine, the University of Iowa, Iowa City, IA 52242, USAStephanie Woo - School of Natural Sciences, Merced, University of California Merced, Merced, CA 95340, USAJacek Topczewski - Department of Biochemistry and Molecular Biology, Medical University of Lublin, PolandJason R Jessen - Department of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USAFang Lin - Department of Anatomy and Cell Biology, Carver College of Medicine, the University of Iowa, Iowa City, IA 52242, USA fang-lin@uiowa.edu
- Resource Type
- Journal article
- Publication Details
- Development (Cambridge), Vol.145(17), p.dev163303
- DOI
- 10.1242/dev.163303
- PMID
- 30082271
- NLM abbreviation
- Development
- ISSN
- 0950-1991
- eISSN
- 1477-9129
- Publisher
- England
- Grant note
- DOI: 10.13039/100006445, name: National Science Foundation, award: IOS-1354457
- Language
- English
- Date published
- 08/06/2018
- Academic Unit
- Anatomy and Cell Biology; Craniofacial Anomalies Research Center
- Record Identifier
- 9984025361302771
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