Cargando…

Activin signaling as an emerging target for therapeutic interventions

After the initial discovery of activins as important regulators of reproduction, novel and diverse roles have been unraveled for them. Activins are expressed in various tissues and have a broad range of activities including the regulation of gonadal function, hormonal homeostasis, growth and differe...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsuchida, Kunihiro, Nakatani, Masashi, Hitachi, Keisuke, Uezumi, Akiyoshi, Sunada, Yoshihide, Ageta, Hiroshi, Inokuchi, Kaoru
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713245/
https://www.ncbi.nlm.nih.gov/pubmed/19538713
http://dx.doi.org/10.1186/1478-811X-7-15
_version_ 1782169565007970304
author Tsuchida, Kunihiro
Nakatani, Masashi
Hitachi, Keisuke
Uezumi, Akiyoshi
Sunada, Yoshihide
Ageta, Hiroshi
Inokuchi, Kaoru
author_facet Tsuchida, Kunihiro
Nakatani, Masashi
Hitachi, Keisuke
Uezumi, Akiyoshi
Sunada, Yoshihide
Ageta, Hiroshi
Inokuchi, Kaoru
author_sort Tsuchida, Kunihiro
collection PubMed
description After the initial discovery of activins as important regulators of reproduction, novel and diverse roles have been unraveled for them. Activins are expressed in various tissues and have a broad range of activities including the regulation of gonadal function, hormonal homeostasis, growth and differentiation of musculoskeletal tissues, regulation of growth and metastasis of cancer cells, proliferation and differentiation of embryonic stem cells, and even higher brain functions. Activins signal through a combination of type I and II transmembrane serine/threonine kinase receptors. Activin receptors are shared by multiple transforming growth factor-β (TGF-β) ligands such as myostatin, growth and differentiation factor-11 and nodal. Thus, although the activity of each ligand is distinct, they are also redundant, both physiologically and pathologically in vivo. Activin receptors activated by ligands phosphorylate the receptor-regulated Smads for TGF-β, Smad2 and 3. The Smad proteins then undergo multimerization with the co-mediator Smad4, and translocate into the nucleus to regulate the transcription of target genes in cooperation with nuclear cofactors. Signaling through receptors and Smads is controlled by multiple mechanisms including phosphorylation and other posttranslational modifications such as sumoylation, which affect potein localization, stability and transcriptional activity. Non-Smad signaling also plays an important role in activin signaling. Extracellularly, follistatin and related proteins bind to activins and related TGF-β ligands, and control the signaling and availability of ligands. The functions of activins through activin receptors are pleiotrophic, cell type-specific and contextual, and they are involved in the etiology and pathogenesis of a variety of diseases. Accordingly, activin signaling may be a target for therapeutic interventions. In this review, we summarize the current knowledge on activin signaling and discuss the potential roles of this pathway as a molecular target of therapy for metabolic diseases, musculoskeletal disorders, cancers and neural damages.
format Text
id pubmed-2713245
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-27132452009-07-21 Activin signaling as an emerging target for therapeutic interventions Tsuchida, Kunihiro Nakatani, Masashi Hitachi, Keisuke Uezumi, Akiyoshi Sunada, Yoshihide Ageta, Hiroshi Inokuchi, Kaoru Cell Commun Signal Review After the initial discovery of activins as important regulators of reproduction, novel and diverse roles have been unraveled for them. Activins are expressed in various tissues and have a broad range of activities including the regulation of gonadal function, hormonal homeostasis, growth and differentiation of musculoskeletal tissues, regulation of growth and metastasis of cancer cells, proliferation and differentiation of embryonic stem cells, and even higher brain functions. Activins signal through a combination of type I and II transmembrane serine/threonine kinase receptors. Activin receptors are shared by multiple transforming growth factor-β (TGF-β) ligands such as myostatin, growth and differentiation factor-11 and nodal. Thus, although the activity of each ligand is distinct, they are also redundant, both physiologically and pathologically in vivo. Activin receptors activated by ligands phosphorylate the receptor-regulated Smads for TGF-β, Smad2 and 3. The Smad proteins then undergo multimerization with the co-mediator Smad4, and translocate into the nucleus to regulate the transcription of target genes in cooperation with nuclear cofactors. Signaling through receptors and Smads is controlled by multiple mechanisms including phosphorylation and other posttranslational modifications such as sumoylation, which affect potein localization, stability and transcriptional activity. Non-Smad signaling also plays an important role in activin signaling. Extracellularly, follistatin and related proteins bind to activins and related TGF-β ligands, and control the signaling and availability of ligands. The functions of activins through activin receptors are pleiotrophic, cell type-specific and contextual, and they are involved in the etiology and pathogenesis of a variety of diseases. Accordingly, activin signaling may be a target for therapeutic interventions. In this review, we summarize the current knowledge on activin signaling and discuss the potential roles of this pathway as a molecular target of therapy for metabolic diseases, musculoskeletal disorders, cancers and neural damages. BioMed Central 2009-06-18 /pmc/articles/PMC2713245/ /pubmed/19538713 http://dx.doi.org/10.1186/1478-811X-7-15 Text en Copyright © 2009 Tsuchida et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Tsuchida, Kunihiro
Nakatani, Masashi
Hitachi, Keisuke
Uezumi, Akiyoshi
Sunada, Yoshihide
Ageta, Hiroshi
Inokuchi, Kaoru
Activin signaling as an emerging target for therapeutic interventions
title Activin signaling as an emerging target for therapeutic interventions
title_full Activin signaling as an emerging target for therapeutic interventions
title_fullStr Activin signaling as an emerging target for therapeutic interventions
title_full_unstemmed Activin signaling as an emerging target for therapeutic interventions
title_short Activin signaling as an emerging target for therapeutic interventions
title_sort activin signaling as an emerging target for therapeutic interventions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713245/
https://www.ncbi.nlm.nih.gov/pubmed/19538713
http://dx.doi.org/10.1186/1478-811X-7-15
work_keys_str_mv AT tsuchidakunihiro activinsignalingasanemergingtargetfortherapeuticinterventions
AT nakatanimasashi activinsignalingasanemergingtargetfortherapeuticinterventions
AT hitachikeisuke activinsignalingasanemergingtargetfortherapeuticinterventions
AT uezumiakiyoshi activinsignalingasanemergingtargetfortherapeuticinterventions
AT sunadayoshihide activinsignalingasanemergingtargetfortherapeuticinterventions
AT agetahiroshi activinsignalingasanemergingtargetfortherapeuticinterventions
AT inokuchikaoru activinsignalingasanemergingtargetfortherapeuticinterventions