Cargando…
WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration
An organizer is defined as a group of cells that secrete extracellular proteins that specify the fate of surrounding cells according to their concentration. Their function during embryogenesis is key in patterning new growing tissues. Although organizers should also participate in adult development...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830089/ https://www.ncbi.nlm.nih.gov/pubmed/33467529 http://dx.doi.org/10.3390/genes12010101 |
_version_ | 1783641326591410176 |
---|---|
author | Pascual-Carreras, Eudald Sureda-Gómez, Miquel Barrull-Mascaró, Ramon Jordà, Natàlia Gelabert, Maria Coronel-Córdoba, Pablo Saló, Emili Adell, Teresa |
author_facet | Pascual-Carreras, Eudald Sureda-Gómez, Miquel Barrull-Mascaró, Ramon Jordà, Natàlia Gelabert, Maria Coronel-Córdoba, Pablo Saló, Emili Adell, Teresa |
author_sort | Pascual-Carreras, Eudald |
collection | PubMed |
description | An organizer is defined as a group of cells that secrete extracellular proteins that specify the fate of surrounding cells according to their concentration. Their function during embryogenesis is key in patterning new growing tissues. Although organizers should also participate in adult development when new structures are regenerated, their presence in adults has only been identified in a few species with striking regenerative abilities, such as planarians. Planarians provide a unique model to understand the function of adult organizers, since the presence of adult pluripotent stem cells provides them with the ability to regenerate any body part. Previous studies have shown that the differential activation of the WNT/β-catenin signal in each wound is fundamental to establish an anterior or a posterior organizer in the corresponding wound. Here, we identify the receptors that mediate the WNT/β-catenin signal in posterior-facing wounds. We found that Wnt1-Fzd1-LRP5/6 signaling is evolutionarily conserved in executing a WNT/β-catenin signal to specify cell fate and to trigger a proliferative response. Our data allow a better understanding of the mechanism through which organizers signal to a “competent” field of cells and integrate the patterning and growth required during de novo formation of organs and tissues. |
format | Online Article Text |
id | pubmed-7830089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78300892021-01-26 WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration Pascual-Carreras, Eudald Sureda-Gómez, Miquel Barrull-Mascaró, Ramon Jordà, Natàlia Gelabert, Maria Coronel-Córdoba, Pablo Saló, Emili Adell, Teresa Genes (Basel) Article An organizer is defined as a group of cells that secrete extracellular proteins that specify the fate of surrounding cells according to their concentration. Their function during embryogenesis is key in patterning new growing tissues. Although organizers should also participate in adult development when new structures are regenerated, their presence in adults has only been identified in a few species with striking regenerative abilities, such as planarians. Planarians provide a unique model to understand the function of adult organizers, since the presence of adult pluripotent stem cells provides them with the ability to regenerate any body part. Previous studies have shown that the differential activation of the WNT/β-catenin signal in each wound is fundamental to establish an anterior or a posterior organizer in the corresponding wound. Here, we identify the receptors that mediate the WNT/β-catenin signal in posterior-facing wounds. We found that Wnt1-Fzd1-LRP5/6 signaling is evolutionarily conserved in executing a WNT/β-catenin signal to specify cell fate and to trigger a proliferative response. Our data allow a better understanding of the mechanism through which organizers signal to a “competent” field of cells and integrate the patterning and growth required during de novo formation of organs and tissues. MDPI 2021-01-15 /pmc/articles/PMC7830089/ /pubmed/33467529 http://dx.doi.org/10.3390/genes12010101 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pascual-Carreras, Eudald Sureda-Gómez, Miquel Barrull-Mascaró, Ramon Jordà, Natàlia Gelabert, Maria Coronel-Córdoba, Pablo Saló, Emili Adell, Teresa WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title | WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title_full | WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title_fullStr | WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title_full_unstemmed | WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title_short | WNT-FRIZZLED-LRP5/6 Signaling Mediates Posterior Fate and Proliferation during Planarian Regeneration |
title_sort | wnt-frizzled-lrp5/6 signaling mediates posterior fate and proliferation during planarian regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830089/ https://www.ncbi.nlm.nih.gov/pubmed/33467529 http://dx.doi.org/10.3390/genes12010101 |
work_keys_str_mv | AT pascualcarreraseudald wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT suredagomezmiquel wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT barrullmascaroramon wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT jordanatalia wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT gelabertmaria wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT coronelcordobapablo wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT saloemili wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration AT adellteresa wntfrizzledlrp56signalingmediatesposteriorfateandproliferationduringplanarianregeneration |