Cargando…

The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease

The Ror-family proteins, Ror1 and Ror2, act as receptors or co-receptors for Wnt5a and its related Wnt proteins to activate non-canonical Wnt signaling. Ror1 and/or Ror2-mediated signaling plays essential roles in regulating cell polarity, migration, proliferation and differentiation during developm...

Descripción completa

Detalles Bibliográficos
Autores principales: Endo, Mitsuharu, Kamizaki, Koki, Minami, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043558/
https://www.ncbi.nlm.nih.gov/pubmed/35493090
http://dx.doi.org/10.3389/fcell.2022.891763
_version_ 1784694908232138752
author Endo, Mitsuharu
Kamizaki, Koki
Minami, Yasuhiro
author_facet Endo, Mitsuharu
Kamizaki, Koki
Minami, Yasuhiro
author_sort Endo, Mitsuharu
collection PubMed
description The Ror-family proteins, Ror1 and Ror2, act as receptors or co-receptors for Wnt5a and its related Wnt proteins to activate non-canonical Wnt signaling. Ror1 and/or Ror2-mediated signaling plays essential roles in regulating cell polarity, migration, proliferation and differentiation during developmental morphogenesis, tissue-/organo-genesis and regeneration of adult tissues following injury. Ror1 and Ror2 are expressed abundantly in developing tissues in an overlapping, yet distinct manner, and their expression in adult tissues is restricted to specific cell types such as tissue stem/progenitor cells. Expression levels of Ror1 and/or Ror2 in the adult tissues are increased following injury, thereby promoting regeneration or repair of these injured tissues. On the other hand, disruption of Wnt5a-Ror2 signaling is implicated in senescence of tissue stem/progenitor cells that is related to the impaired regeneration capacity of aged tissues. In fact, Ror1 and Ror2 are implicated in age-related diseases, including tissue fibrosis, atherosclerosis (or arteriosclerosis), neurodegenerative diseases, and cancers. In these diseases, enhanced and/or sustained (chronic) expression of Ror1 and/or Ror2 is observed, and they might contribute to the progression of these diseases through Wnt5a-dependent and -independent manners. In this article, we overview recent advances in our understanding of the roles of Ror1 and Ror2-mediated signaling in the development, tissue regeneration and age-related diseases, and discuss their potential to be therapeutic targets for chronic inflammatory diseases and cancers.
format Online
Article
Text
id pubmed-9043558
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90435582022-04-28 The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease Endo, Mitsuharu Kamizaki, Koki Minami, Yasuhiro Front Cell Dev Biol Cell and Developmental Biology The Ror-family proteins, Ror1 and Ror2, act as receptors or co-receptors for Wnt5a and its related Wnt proteins to activate non-canonical Wnt signaling. Ror1 and/or Ror2-mediated signaling plays essential roles in regulating cell polarity, migration, proliferation and differentiation during developmental morphogenesis, tissue-/organo-genesis and regeneration of adult tissues following injury. Ror1 and Ror2 are expressed abundantly in developing tissues in an overlapping, yet distinct manner, and their expression in adult tissues is restricted to specific cell types such as tissue stem/progenitor cells. Expression levels of Ror1 and/or Ror2 in the adult tissues are increased following injury, thereby promoting regeneration or repair of these injured tissues. On the other hand, disruption of Wnt5a-Ror2 signaling is implicated in senescence of tissue stem/progenitor cells that is related to the impaired regeneration capacity of aged tissues. In fact, Ror1 and Ror2 are implicated in age-related diseases, including tissue fibrosis, atherosclerosis (or arteriosclerosis), neurodegenerative diseases, and cancers. In these diseases, enhanced and/or sustained (chronic) expression of Ror1 and/or Ror2 is observed, and they might contribute to the progression of these diseases through Wnt5a-dependent and -independent manners. In this article, we overview recent advances in our understanding of the roles of Ror1 and Ror2-mediated signaling in the development, tissue regeneration and age-related diseases, and discuss their potential to be therapeutic targets for chronic inflammatory diseases and cancers. Frontiers Media S.A. 2022-04-13 /pmc/articles/PMC9043558/ /pubmed/35493090 http://dx.doi.org/10.3389/fcell.2022.891763 Text en Copyright © 2022 Endo, Kamizaki and Minami. https://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
Endo, Mitsuharu
Kamizaki, Koki
Minami, Yasuhiro
The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title_full The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title_fullStr The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title_full_unstemmed The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title_short The Ror-Family Receptors in Development, Tissue Regeneration and Age-Related Disease
title_sort ror-family receptors in development, tissue regeneration and age-related disease
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043558/
https://www.ncbi.nlm.nih.gov/pubmed/35493090
http://dx.doi.org/10.3389/fcell.2022.891763
work_keys_str_mv AT endomitsuharu therorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease
AT kamizakikoki therorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease
AT minamiyasuhiro therorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease
AT endomitsuharu rorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease
AT kamizakikoki rorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease
AT minamiyasuhiro rorfamilyreceptorsindevelopmenttissueregenerationandagerelateddisease