Cargando…

Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro

Here, we investigated the role of the Wnt/β-catenin signaling pathway in chicken primordial germ cells (PGCs) in vitro. We confirmed the expression of Wnt signaling pathway-related genes and the localization of β-catenin in the nucleus, revealing that this pathway is potentially activated in chicken...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Hyung Chul, Lim, Sumi, Han, Jae Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062643/
https://www.ncbi.nlm.nih.gov/pubmed/27687983
http://dx.doi.org/10.1038/srep34510
_version_ 1782459820453920768
author Lee, Hyung Chul
Lim, Sumi
Han, Jae Yong
author_facet Lee, Hyung Chul
Lim, Sumi
Han, Jae Yong
author_sort Lee, Hyung Chul
collection PubMed
description Here, we investigated the role of the Wnt/β-catenin signaling pathway in chicken primordial germ cells (PGCs) in vitro. We confirmed the expression of Wnt signaling pathway-related genes and the localization of β-catenin in the nucleus, revealing that this pathway is potentially activated in chicken PGCs. Then, using the single-cell pick-up assay, we examined the proliferative capacity of cultured PGCs in response to Wnt ligands, a β-catenin-mediated Wnt signaling activator (6-bromoindirubin-3′-oxime [BIO]) or inhibitor (JW74), in the presence or absence of basic fibroblast growth factor (bFGF). WNT1, WNT3A, and BIO promoted the proliferation of chicken PGCs similarly to bFGF, whereas JW74 inhibited this proliferation. Meanwhile, such treatments in combination with bFGF did not show a synergistic effect. bFGF treatment could not rescue PGC proliferation in the presence of JW74. In addition, we confirmed the translocation of β-catenin into the nucleus by the addition of bFGF after JW74 treatment. These results indicate that there is signaling crosstalk between FGF and Wnt, and that β-catenin acts on PGC proliferation downstream of bFGF. In conclusion, our study suggests that Wnt signaling enhances the proliferation of chicken PGCs via the stabilization of β-catenin and activation of its downstream genes.
format Online
Article
Text
id pubmed-5062643
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50626432016-10-24 Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro Lee, Hyung Chul Lim, Sumi Han, Jae Yong Sci Rep Article Here, we investigated the role of the Wnt/β-catenin signaling pathway in chicken primordial germ cells (PGCs) in vitro. We confirmed the expression of Wnt signaling pathway-related genes and the localization of β-catenin in the nucleus, revealing that this pathway is potentially activated in chicken PGCs. Then, using the single-cell pick-up assay, we examined the proliferative capacity of cultured PGCs in response to Wnt ligands, a β-catenin-mediated Wnt signaling activator (6-bromoindirubin-3′-oxime [BIO]) or inhibitor (JW74), in the presence or absence of basic fibroblast growth factor (bFGF). WNT1, WNT3A, and BIO promoted the proliferation of chicken PGCs similarly to bFGF, whereas JW74 inhibited this proliferation. Meanwhile, such treatments in combination with bFGF did not show a synergistic effect. bFGF treatment could not rescue PGC proliferation in the presence of JW74. In addition, we confirmed the translocation of β-catenin into the nucleus by the addition of bFGF after JW74 treatment. These results indicate that there is signaling crosstalk between FGF and Wnt, and that β-catenin acts on PGC proliferation downstream of bFGF. In conclusion, our study suggests that Wnt signaling enhances the proliferation of chicken PGCs via the stabilization of β-catenin and activation of its downstream genes. Nature Publishing Group 2016-09-30 /pmc/articles/PMC5062643/ /pubmed/27687983 http://dx.doi.org/10.1038/srep34510 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Hyung Chul
Lim, Sumi
Han, Jae Yong
Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title_full Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title_fullStr Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title_full_unstemmed Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title_short Wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
title_sort wnt/β-catenin signaling pathway activation is required for proliferation of chicken primordial germ cells in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062643/
https://www.ncbi.nlm.nih.gov/pubmed/27687983
http://dx.doi.org/10.1038/srep34510
work_keys_str_mv AT leehyungchul wntbcateninsignalingpathwayactivationisrequiredforproliferationofchickenprimordialgermcellsinvitro
AT limsumi wntbcateninsignalingpathwayactivationisrequiredforproliferationofchickenprimordialgermcellsinvitro
AT hanjaeyong wntbcateninsignalingpathwayactivationisrequiredforproliferationofchickenprimordialgermcellsinvitro