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TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction

Wnt signaling pathway plays indispensable roles in embryonic development and adult tissue homeostasis. However, the regulatory mechanisms involved in Wnt ligand trafficking within and secretion from the signal sending cells is still relatively uncharacterized. Here, we discover a novel regulator of...

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Detalles Bibliográficos
Autores principales: Li, Binbin, Niswander, Lee A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726220/
https://www.ncbi.nlm.nih.gov/pubmed/33324648
http://dx.doi.org/10.3389/fcell.2020.599890
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author Li, Binbin
Niswander, Lee A.
author_facet Li, Binbin
Niswander, Lee A.
author_sort Li, Binbin
collection PubMed
description Wnt signaling pathway plays indispensable roles in embryonic development and adult tissue homeostasis. However, the regulatory mechanisms involved in Wnt ligand trafficking within and secretion from the signal sending cells is still relatively uncharacterized. Here, we discover a novel regulator of Wnt signaling pathway called transmembrane protein 132A (TMEM132A). Our evidence shows a physical and functional interaction of TMEM132A with the Wnt ligand transporting protein Wntless (WLS). We show that TMEM132A stabilizes Wnt ligand, enhances WLS–Wnt ligand interaction, and activates the Wnt signaling pathway. Our results shed new light on the cellular mechanism underlying the fundamental aspect of WNT secretion from Wnt signal sending cells.
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spelling pubmed-77262202020-12-14 TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction Li, Binbin Niswander, Lee A. Front Cell Dev Biol Cell and Developmental Biology Wnt signaling pathway plays indispensable roles in embryonic development and adult tissue homeostasis. However, the regulatory mechanisms involved in Wnt ligand trafficking within and secretion from the signal sending cells is still relatively uncharacterized. Here, we discover a novel regulator of Wnt signaling pathway called transmembrane protein 132A (TMEM132A). Our evidence shows a physical and functional interaction of TMEM132A with the Wnt ligand transporting protein Wntless (WLS). We show that TMEM132A stabilizes Wnt ligand, enhances WLS–Wnt ligand interaction, and activates the Wnt signaling pathway. Our results shed new light on the cellular mechanism underlying the fundamental aspect of WNT secretion from Wnt signal sending cells. Frontiers Media S.A. 2020-11-26 /pmc/articles/PMC7726220/ /pubmed/33324648 http://dx.doi.org/10.3389/fcell.2020.599890 Text en Copyright © 2020 Li and Niswander. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Li, Binbin
Niswander, Lee A.
TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title_full TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title_fullStr TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title_full_unstemmed TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title_short TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
title_sort tmem132a, a novel wnt signaling pathway regulator through wntless (wls) interaction
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726220/
https://www.ncbi.nlm.nih.gov/pubmed/33324648
http://dx.doi.org/10.3389/fcell.2020.599890
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