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A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand

Fibroblast growth factor (FGF) is a multifunctional protein that exhibits a wide range of biological effects. Most commonly, it acts as a mitogen, but it also has regulatory, morphological, and endocrine effects. The four receptor subtypes of FGF are activated by more than 20 different FGF ligands....

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Autores principales: Yonehara, Ryo, Kumachi, Shigefumi, Kashiwagi, Kenji, Wakabayashi-Nakao, Kanako, Motohashi, Maiko, Murakami, Taihei, Yanagisawa, Teruhiko, Arai, Hidenao, Murakami, Akikazu, Ueno, Yukio, Nemoto, Naoto, Tsuchiya, Masayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852558/
https://www.ncbi.nlm.nih.gov/pubmed/36529290
http://dx.doi.org/10.1016/j.jbc.2022.102804
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author Yonehara, Ryo
Kumachi, Shigefumi
Kashiwagi, Kenji
Wakabayashi-Nakao, Kanako
Motohashi, Maiko
Murakami, Taihei
Yanagisawa, Teruhiko
Arai, Hidenao
Murakami, Akikazu
Ueno, Yukio
Nemoto, Naoto
Tsuchiya, Masayuki
author_facet Yonehara, Ryo
Kumachi, Shigefumi
Kashiwagi, Kenji
Wakabayashi-Nakao, Kanako
Motohashi, Maiko
Murakami, Taihei
Yanagisawa, Teruhiko
Arai, Hidenao
Murakami, Akikazu
Ueno, Yukio
Nemoto, Naoto
Tsuchiya, Masayuki
author_sort Yonehara, Ryo
collection PubMed
description Fibroblast growth factor (FGF) is a multifunctional protein that exhibits a wide range of biological effects. Most commonly, it acts as a mitogen, but it also has regulatory, morphological, and endocrine effects. The four receptor subtypes of FGF are activated by more than 20 different FGF ligands. FGF2, one of the FGF ligands, is an essential factor for cell culture in stem cells for regenerative medicine; however, recombinant FGF2 is extremely unstable. Here, we successfully generated homobivalent agonistic single-domain antibodies (variable domain of heavy chain of heavy chain antibodies referred to as VHHs) that bind to domain III and induce activation of the FGF receptor 1 and thus transduce intracellular signaling. This agonistic VHH has similar biological activity (EC(50)) as the natural FGF2 ligand. Furthermore, we determined that the agonistic VHH could support the proliferation of human-induced pluripotent stem cells (PSCs) and human mesenchymal stem cells, which are PSCs for regenerative medicine. In addition, the agonistic VHH could maintain the ability of mesenchymal stem cells to differentiate into adipocytes or osteocytes, indicating that it could maintain the properties of PSCs. These results suggest that the VHH agonist may function as an FGF2 mimetic in cell preparation of stem cells for regenerative medicine with better cost effectiveness.
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spelling pubmed-98525582023-01-24 A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand Yonehara, Ryo Kumachi, Shigefumi Kashiwagi, Kenji Wakabayashi-Nakao, Kanako Motohashi, Maiko Murakami, Taihei Yanagisawa, Teruhiko Arai, Hidenao Murakami, Akikazu Ueno, Yukio Nemoto, Naoto Tsuchiya, Masayuki J Biol Chem Research Article Fibroblast growth factor (FGF) is a multifunctional protein that exhibits a wide range of biological effects. Most commonly, it acts as a mitogen, but it also has regulatory, morphological, and endocrine effects. The four receptor subtypes of FGF are activated by more than 20 different FGF ligands. FGF2, one of the FGF ligands, is an essential factor for cell culture in stem cells for regenerative medicine; however, recombinant FGF2 is extremely unstable. Here, we successfully generated homobivalent agonistic single-domain antibodies (variable domain of heavy chain of heavy chain antibodies referred to as VHHs) that bind to domain III and induce activation of the FGF receptor 1 and thus transduce intracellular signaling. This agonistic VHH has similar biological activity (EC(50)) as the natural FGF2 ligand. Furthermore, we determined that the agonistic VHH could support the proliferation of human-induced pluripotent stem cells (PSCs) and human mesenchymal stem cells, which are PSCs for regenerative medicine. In addition, the agonistic VHH could maintain the ability of mesenchymal stem cells to differentiate into adipocytes or osteocytes, indicating that it could maintain the properties of PSCs. These results suggest that the VHH agonist may function as an FGF2 mimetic in cell preparation of stem cells for regenerative medicine with better cost effectiveness. American Society for Biochemistry and Molecular Biology 2022-12-15 /pmc/articles/PMC9852558/ /pubmed/36529290 http://dx.doi.org/10.1016/j.jbc.2022.102804 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Yonehara, Ryo
Kumachi, Shigefumi
Kashiwagi, Kenji
Wakabayashi-Nakao, Kanako
Motohashi, Maiko
Murakami, Taihei
Yanagisawa, Teruhiko
Arai, Hidenao
Murakami, Akikazu
Ueno, Yukio
Nemoto, Naoto
Tsuchiya, Masayuki
A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title_full A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title_fullStr A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title_full_unstemmed A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title_short A novel agonist with homobivalent single-domain antibodies that bind the FGF receptor 1 domain III functions as an FGF2 ligand
title_sort novel agonist with homobivalent single-domain antibodies that bind the fgf receptor 1 domain iii functions as an fgf2 ligand
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852558/
https://www.ncbi.nlm.nih.gov/pubmed/36529290
http://dx.doi.org/10.1016/j.jbc.2022.102804
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