Cargando…

Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes

Grb2-associated binder (Gab) docking proteins regulate signals downstream of a variety of growth factors and receptor tyrosine kinases. Neuregulin-1 (NRG-1), a member of epidermal growth factor family, plays a critical role for cardiomyocyte proliferation and prevention of heart failure via ErbB rec...

Descripción completa

Detalles Bibliográficos
Autores principales: Yasui, Taku, Masaki, Takeshi, Arita, Yoh, Ishibashi, Tomohiko, Inagaki, Tadakatsu, Okazawa, Makoto, Oka, Toru, Shioyama, Wataru, Yamauchi-Takihara, Keiko, Komuro, Issei, Sakata, Yasushi, Nakaoka, Yoshikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115770/
https://www.ncbi.nlm.nih.gov/pubmed/27861634
http://dx.doi.org/10.1371/journal.pone.0166710
_version_ 1782468568883920896
author Yasui, Taku
Masaki, Takeshi
Arita, Yoh
Ishibashi, Tomohiko
Inagaki, Tadakatsu
Okazawa, Makoto
Oka, Toru
Shioyama, Wataru
Yamauchi-Takihara, Keiko
Komuro, Issei
Sakata, Yasushi
Nakaoka, Yoshikazu
author_facet Yasui, Taku
Masaki, Takeshi
Arita, Yoh
Ishibashi, Tomohiko
Inagaki, Tadakatsu
Okazawa, Makoto
Oka, Toru
Shioyama, Wataru
Yamauchi-Takihara, Keiko
Komuro, Issei
Sakata, Yasushi
Nakaoka, Yoshikazu
author_sort Yasui, Taku
collection PubMed
description Grb2-associated binder (Gab) docking proteins regulate signals downstream of a variety of growth factors and receptor tyrosine kinases. Neuregulin-1 (NRG-1), a member of epidermal growth factor family, plays a critical role for cardiomyocyte proliferation and prevention of heart failure via ErbB receptors. We previously reported that Gab1 and Gab2 in the myocardium are essential for maintenance of myocardial function in the postnatal heart via transmission of NRG-1/ErbB-signaling through analysis of Gab1/Gab2 cardiomyocyte-specific double knockout mice. In that study, we also found that there is an unknown high-molecular weight (high-MW) Gab1 isoform (120 kDa) expressed exclusively in the heart, in addition to the ubiquitously expressed low-MW (100 kDa) Gab1. However, the high-MW Gab1 has been molecularly ill-defined to date. Here, we identified the high-MW Gab1 as a striated muscle-specific isoform. The high-MW Gab1 has an extra exon encoding 27 amino acid residues between the already-known 3(rd) and 4th exons of the ubiquitously expressed low-MW Gab1. Expression analysis by RT-PCR and immunostaining with the antibody specific for the high-MW Gab1 demonstrate that the high-MW Gab1 isoform is exclusively expressed in striated muscle including heart and skeletal muscle. The ratio of high-MW Gab1/ total Gab1 mRNAs increased along with heart development. The high-MW Gab1 isoform in heart underwent tyrosine-phosphorylation exclusively after intravenous administration of NRG-1, among several growth factors. Adenovirus-mediated overexpression of the high-MW Gab1 induces more sustained activation of AKT after stimulation with NRG-1 in cardiomyocytes compared with that of β-galactosidase. On the contrary, siRNA-mediated knockdown of the high-MW Gab1 significantly attenuated AKT activation after stimulation with NRG-1 in cardiomyocytes. Taken together, these findings suggest that the striated muscle-specific high-MW isoform of Gab1 has a crucial role for NRG-1/ErbB signaling in cardiomyocytes.
format Online
Article
Text
id pubmed-5115770
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-51157702016-12-08 Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes Yasui, Taku Masaki, Takeshi Arita, Yoh Ishibashi, Tomohiko Inagaki, Tadakatsu Okazawa, Makoto Oka, Toru Shioyama, Wataru Yamauchi-Takihara, Keiko Komuro, Issei Sakata, Yasushi Nakaoka, Yoshikazu PLoS One Research Article Grb2-associated binder (Gab) docking proteins regulate signals downstream of a variety of growth factors and receptor tyrosine kinases. Neuregulin-1 (NRG-1), a member of epidermal growth factor family, plays a critical role for cardiomyocyte proliferation and prevention of heart failure via ErbB receptors. We previously reported that Gab1 and Gab2 in the myocardium are essential for maintenance of myocardial function in the postnatal heart via transmission of NRG-1/ErbB-signaling through analysis of Gab1/Gab2 cardiomyocyte-specific double knockout mice. In that study, we also found that there is an unknown high-molecular weight (high-MW) Gab1 isoform (120 kDa) expressed exclusively in the heart, in addition to the ubiquitously expressed low-MW (100 kDa) Gab1. However, the high-MW Gab1 has been molecularly ill-defined to date. Here, we identified the high-MW Gab1 as a striated muscle-specific isoform. The high-MW Gab1 has an extra exon encoding 27 amino acid residues between the already-known 3(rd) and 4th exons of the ubiquitously expressed low-MW Gab1. Expression analysis by RT-PCR and immunostaining with the antibody specific for the high-MW Gab1 demonstrate that the high-MW Gab1 isoform is exclusively expressed in striated muscle including heart and skeletal muscle. The ratio of high-MW Gab1/ total Gab1 mRNAs increased along with heart development. The high-MW Gab1 isoform in heart underwent tyrosine-phosphorylation exclusively after intravenous administration of NRG-1, among several growth factors. Adenovirus-mediated overexpression of the high-MW Gab1 induces more sustained activation of AKT after stimulation with NRG-1 in cardiomyocytes compared with that of β-galactosidase. On the contrary, siRNA-mediated knockdown of the high-MW Gab1 significantly attenuated AKT activation after stimulation with NRG-1 in cardiomyocytes. Taken together, these findings suggest that the striated muscle-specific high-MW isoform of Gab1 has a crucial role for NRG-1/ErbB signaling in cardiomyocytes. Public Library of Science 2016-11-18 /pmc/articles/PMC5115770/ /pubmed/27861634 http://dx.doi.org/10.1371/journal.pone.0166710 Text en © 2016 Yasui et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yasui, Taku
Masaki, Takeshi
Arita, Yoh
Ishibashi, Tomohiko
Inagaki, Tadakatsu
Okazawa, Makoto
Oka, Toru
Shioyama, Wataru
Yamauchi-Takihara, Keiko
Komuro, Issei
Sakata, Yasushi
Nakaoka, Yoshikazu
Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title_full Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title_fullStr Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title_full_unstemmed Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title_short Molecular Characterization of Striated Muscle-Specific Gab1 Isoform as a Critical Signal Transducer for Neuregulin-1/ErbB Signaling in Cardiomyocytes
title_sort molecular characterization of striated muscle-specific gab1 isoform as a critical signal transducer for neuregulin-1/erbb signaling in cardiomyocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115770/
https://www.ncbi.nlm.nih.gov/pubmed/27861634
http://dx.doi.org/10.1371/journal.pone.0166710
work_keys_str_mv AT yasuitaku molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT masakitakeshi molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT aritayoh molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT ishibashitomohiko molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT inagakitadakatsu molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT okazawamakoto molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT okatoru molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT shioyamawataru molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT yamauchitakiharakeiko molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT komuroissei molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT sakatayasushi molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes
AT nakaokayoshikazu molecularcharacterizationofstriatedmusclespecificgab1isoformasacriticalsignaltransducerforneuregulin1erbbsignalingincardiomyocytes