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Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach

Hepatocyte growth factor (HGF) is secreted as an inactive single-chain HGF (scHGF); however, only proteolytically processed two-chain HGF (tcHGF) can activate the MET receptor. We investigated the localization of tcHGF and activated/phosphorylated MET (pMET) using a tcHGF-specific antibody. In day 1...

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Autores principales: Jangphattananont, Nawaphat, Sato, Hiroki, Imamura, Ryu, Sakai, Katsuya, Terakado, Yumi, Murakami, Kazuhiro, Barker, Nick, Oshima, Hiroko, Oshima, Masanobu, Takagi, Junichi, Kato, Yukinari, Yano, Seiji, Matsumoto, Kunio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628191/
https://www.ncbi.nlm.nih.gov/pubmed/31212972
http://dx.doi.org/10.3390/ijms20122955
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author Jangphattananont, Nawaphat
Sato, Hiroki
Imamura, Ryu
Sakai, Katsuya
Terakado, Yumi
Murakami, Kazuhiro
Barker, Nick
Oshima, Hiroko
Oshima, Masanobu
Takagi, Junichi
Kato, Yukinari
Yano, Seiji
Matsumoto, Kunio
author_facet Jangphattananont, Nawaphat
Sato, Hiroki
Imamura, Ryu
Sakai, Katsuya
Terakado, Yumi
Murakami, Kazuhiro
Barker, Nick
Oshima, Hiroko
Oshima, Masanobu
Takagi, Junichi
Kato, Yukinari
Yano, Seiji
Matsumoto, Kunio
author_sort Jangphattananont, Nawaphat
collection PubMed
description Hepatocyte growth factor (HGF) is secreted as an inactive single-chain HGF (scHGF); however, only proteolytically processed two-chain HGF (tcHGF) can activate the MET receptor. We investigated the localization of tcHGF and activated/phosphorylated MET (pMET) using a tcHGF-specific antibody. In day 16.5 mouse embryos, total HGF (scHGF + tcHGF) was mainly localized in smooth muscle cells close to, but separate from, MET-positive epithelial cells in endodermal organs, including the stomach. In the adult stomach, total HGF was localized in smooth muscle cells, and tcHGF was mainly localized in the glandular base region. Immunostaining for pMET and Lgr5-driven green fluorescent protein (GFP) indicated that pMET localization overlapped with Lgr5(+) gastric stem cells. HGF promoted organoid formation similar to EGF, indicating the potential for HGF to promote the survival and growth of gastric stem cells. pMET and tcHGF localizations changed during regeneration following gastric injury. These results indicate that MET is constantly activated in gastric stem cells and that the localization of pMET differs from the primary localization of precursor HGF but has a close relationship to tcHGF. Our results suggest the importance of the microenvironmental generation of tcHGF in the regulation of development, regeneration, and stem cell behavior.
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spelling pubmed-66281912019-07-23 Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach Jangphattananont, Nawaphat Sato, Hiroki Imamura, Ryu Sakai, Katsuya Terakado, Yumi Murakami, Kazuhiro Barker, Nick Oshima, Hiroko Oshima, Masanobu Takagi, Junichi Kato, Yukinari Yano, Seiji Matsumoto, Kunio Int J Mol Sci Article Hepatocyte growth factor (HGF) is secreted as an inactive single-chain HGF (scHGF); however, only proteolytically processed two-chain HGF (tcHGF) can activate the MET receptor. We investigated the localization of tcHGF and activated/phosphorylated MET (pMET) using a tcHGF-specific antibody. In day 16.5 mouse embryos, total HGF (scHGF + tcHGF) was mainly localized in smooth muscle cells close to, but separate from, MET-positive epithelial cells in endodermal organs, including the stomach. In the adult stomach, total HGF was localized in smooth muscle cells, and tcHGF was mainly localized in the glandular base region. Immunostaining for pMET and Lgr5-driven green fluorescent protein (GFP) indicated that pMET localization overlapped with Lgr5(+) gastric stem cells. HGF promoted organoid formation similar to EGF, indicating the potential for HGF to promote the survival and growth of gastric stem cells. pMET and tcHGF localizations changed during regeneration following gastric injury. These results indicate that MET is constantly activated in gastric stem cells and that the localization of pMET differs from the primary localization of precursor HGF but has a close relationship to tcHGF. Our results suggest the importance of the microenvironmental generation of tcHGF in the regulation of development, regeneration, and stem cell behavior. MDPI 2019-06-17 /pmc/articles/PMC6628191/ /pubmed/31212972 http://dx.doi.org/10.3390/ijms20122955 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jangphattananont, Nawaphat
Sato, Hiroki
Imamura, Ryu
Sakai, Katsuya
Terakado, Yumi
Murakami, Kazuhiro
Barker, Nick
Oshima, Hiroko
Oshima, Masanobu
Takagi, Junichi
Kato, Yukinari
Yano, Seiji
Matsumoto, Kunio
Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title_full Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title_fullStr Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title_full_unstemmed Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title_short Distinct Localization of Mature HGF from its Precursor Form in Developing and Repairing the Stomach
title_sort distinct localization of mature hgf from its precursor form in developing and repairing the stomach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628191/
https://www.ncbi.nlm.nih.gov/pubmed/31212972
http://dx.doi.org/10.3390/ijms20122955
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