Open AccessGlypican 4 and Mmp14 interact in regulating the migration of anterior endodermal cells by limiting extracellular matrix deposition
Author(s) -
Bo Hu,
Yixiao Gao,
Lauren Davies,
Stephanie Woo,
Jacek Topczewski,
Jason R. Jessen,
Lin Fang
Publication year - 2018
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.163303
Subject(s) - endoderm , microbiology and biotechnology , extracellular matrix , gastrulation , fibronectin , mesoderm , cell migration , biology , embryogenesis , embryonic stem cell , embryo , cell , genetics , gene
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 gpc4 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.