Sulf1 has ligand-dependent effects on canonical and non-canonical Wnt signalling

被引:20
作者
Fellgett, Simon W. [1 ]
Maguire, Richard J. [1 ]
Pownall, Mary Elizabeth [1 ]
机构
[1] Univ York, Dept Biol, York YO10 5YW, N Yorkshire, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Morphogen; Development; Cell signalling; Pronephros; 6-O-endosulfatase; Heparan sulfate; HSPG; Wnt; CELL POLARITY PATHWAY; VENTRAL SPINAL-CORD; HEPARAN-SULFATE; XENOPUS-EMBRYOS; CONVERGENT EXTENSION; SPEMANN ORGANIZER; BETA-CATENIN; MESODERM INDUCTION; MORPHOGEN GRADIENT; AXIS FORMATION;
D O I
10.1242/jcs.164467
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Wnt signalling plays essential roles during embryonic development and is known to be mis-regulated in human disease. There are many molecular mechanisms that ensure tight regulation of Wnt activity. One such regulator is the heparan-sulfate-specific 6-O-endosulfatase Sulf1. Sulf1 acts extracellularly to modify the structure of heparan sulfate chains to affect the bio-availability of Wnt ligands. Sulf1 could, therefore, influence the formation of Wnt signalling complexes to modulate the activation of both canonical and non-canonical pathways. In this study, we use well-established assays in Xenopus to investigate the ability of Sulf1 to modify canonical and non-canonical Wnt signalling. In addition, we model the ability of Sulf1 to influence morphogen gradients using fluorescently tagged Wnt ligands in ectodermal explants. We show that Sulf1 overexpression has ligand-specific effects on Wnt signalling: it affects membrane accumulation and extracellular levels of tagged Wnt8a and Wnt11b ligands differently, and inhibits the activity of canonical Wnt8a but enhances the activity of non-canonical Wnt11b.
引用
收藏
页码:1408 / 1421
页数:14
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