Extracellular carriers control lipid-dependent secretion, delivery, and activity of WNT morphogens

WNT morphogens trigger signaling pathways fundamental for embryogenesis, regeneration, and cancer. WNTs are modified with palmitoleate, which is critical for binding Frizzled (FZD) receptors and activating signaling. However, it is unknown how WNTs are released and spread from cells, given their str...

Full description

Saved in:
Bibliographic Details
Published inDevelopmental cell Vol. 59; no. 2; pp. 244 - 261.e6
Main Authors de Almeida Magalhaes, Taciani, Liu, Jingjing, Chan, Charlene, Borges, Kleiton Silva, Zhang, Jiuchun, Kane, Andrew J, Wierbowski, Bradley M, Ge, Yunhui, Liu, Zhiwen, Mannam, Prabhath, Zeve, Daniel, Weiss, Ron, Breault, David T, Huang, Pengxiang, Salic, Adrian
Format Journal Article
LanguageEnglish
Published United States 22.01.2024
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:WNT morphogens trigger signaling pathways fundamental for embryogenesis, regeneration, and cancer. WNTs are modified with palmitoleate, which is critical for binding Frizzled (FZD) receptors and activating signaling. However, it is unknown how WNTs are released and spread from cells, given their strong lipid-dependent membrane attachment. We demonstrate that secreted FZD-related proteins and WNT inhibitory factor 1 are WNT carriers, potently releasing lipidated WNTs and forming active soluble complexes. WNT release occurs by direct handoff from the membrane protein WNTLESS to the carriers. In turn, carriers donate WNTs to glypicans and FZDs involved in WNT reception and to the NOTUM hydrolase, which antagonizes WNTs by lipid moiety removal. WNT transfer from carriers to FZDs is greatly facilitated by glypicans that serve as essential co-receptors in Wnt signaling. Thus, an extracellular network of carriers dynamically controls secretion, posttranslational regulation, and delivery of WNT morphogens, with important practical implications for regenerative medicine.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1534-5807
1878-1551
DOI:10.1016/j.devcel.2023.11.027