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Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells

Fucosylated proteins are widely used as biomarkers of cancer and inflammation. Fucosylated alpha-fetoprotein (AFP-L3) is a specific biomarker for hepatocellular carcinoma. We previously showed that increases in serum AFP-L3 levels depend on increased expression of fucosylation-regulatory genes and a...

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Autores principales: Muranaka, Mizuki, Takamatsu, Shinji, Ouchida, Tsunenori, Kanazawa, Yuri, Kondo, Jumpei, Nakagawa, Tsutomu, Egashira, Yuriko, Fukagawa, Koji, Gu, Jianguo, Okamoto, Toru, Kamada, Yoshihiro, Miyoshi, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138374/
https://www.ncbi.nlm.nih.gov/pubmed/37108200
http://dx.doi.org/10.3390/ijms24087037
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author Muranaka, Mizuki
Takamatsu, Shinji
Ouchida, Tsunenori
Kanazawa, Yuri
Kondo, Jumpei
Nakagawa, Tsutomu
Egashira, Yuriko
Fukagawa, Koji
Gu, Jianguo
Okamoto, Toru
Kamada, Yoshihiro
Miyoshi, Eiji
author_facet Muranaka, Mizuki
Takamatsu, Shinji
Ouchida, Tsunenori
Kanazawa, Yuri
Kondo, Jumpei
Nakagawa, Tsutomu
Egashira, Yuriko
Fukagawa, Koji
Gu, Jianguo
Okamoto, Toru
Kamada, Yoshihiro
Miyoshi, Eiji
author_sort Muranaka, Mizuki
collection PubMed
description Fucosylated proteins are widely used as biomarkers of cancer and inflammation. Fucosylated alpha-fetoprotein (AFP-L3) is a specific biomarker for hepatocellular carcinoma. We previously showed that increases in serum AFP-L3 levels depend on increased expression of fucosylation-regulatory genes and abnormal transport of fucosylated proteins in cancer cells. In normal hepatocytes, fucosylated proteins are selectively secreted in the bile duct but not blood. In cases of cancer cells without cellular polarity, this selective secretion system is destroyed. Here, we aimed to identify cargo proteins involved in the selective secretion of fucosylated proteins, such as AFP-L3, into bile duct-like structures in HepG2 hepatoma cells, which have cellular polarity like, in part, normal hepatocytes. α1-6 Fucosyltransferase (FUT8) is a key enzyme to synthesize core fucose and produce AFP-L3. Firstly, we knocked out the FUT8 gene in HepG2 cells and investigated the effects on the secretion of AFP-L3. AFP-L3 accumulated in bile duct-like structures in HepG2 cells, and this phenomenon was diminished by FUT8 knockout, suggesting that HepG2 cells have cargo proteins for AFP-L3. To identify cargo proteins involved in the secretion of fucosylated proteins in HepG2 cells, immunoprecipitation and the proteomic Strep-tag system experiments followed by mass spectrometry analyses were performed. As a result of proteomic analysis, seven kinds of lectin-like molecules were identified, and we selected vesicular integral membrane protein gene VIP36 as a candidate of the cargo protein that interacts with the α1-6 fucosylation (core fucose) on N-glycan according to bibliographical consideration. Expectedly, the knockout of the VIP36 gene in HepG2 cells suppressed the secretion of AFP-L3 and other fucosylated proteins, such as fucosylated alpha-1 antitrypsin, into bile duct-like structures. We propose that VIP36 could be a cargo protein involved in the apical secretion of fucosylated proteins in HepG2 cells.
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spelling pubmed-101383742023-04-28 Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells Muranaka, Mizuki Takamatsu, Shinji Ouchida, Tsunenori Kanazawa, Yuri Kondo, Jumpei Nakagawa, Tsutomu Egashira, Yuriko Fukagawa, Koji Gu, Jianguo Okamoto, Toru Kamada, Yoshihiro Miyoshi, Eiji Int J Mol Sci Article Fucosylated proteins are widely used as biomarkers of cancer and inflammation. Fucosylated alpha-fetoprotein (AFP-L3) is a specific biomarker for hepatocellular carcinoma. We previously showed that increases in serum AFP-L3 levels depend on increased expression of fucosylation-regulatory genes and abnormal transport of fucosylated proteins in cancer cells. In normal hepatocytes, fucosylated proteins are selectively secreted in the bile duct but not blood. In cases of cancer cells without cellular polarity, this selective secretion system is destroyed. Here, we aimed to identify cargo proteins involved in the selective secretion of fucosylated proteins, such as AFP-L3, into bile duct-like structures in HepG2 hepatoma cells, which have cellular polarity like, in part, normal hepatocytes. α1-6 Fucosyltransferase (FUT8) is a key enzyme to synthesize core fucose and produce AFP-L3. Firstly, we knocked out the FUT8 gene in HepG2 cells and investigated the effects on the secretion of AFP-L3. AFP-L3 accumulated in bile duct-like structures in HepG2 cells, and this phenomenon was diminished by FUT8 knockout, suggesting that HepG2 cells have cargo proteins for AFP-L3. To identify cargo proteins involved in the secretion of fucosylated proteins in HepG2 cells, immunoprecipitation and the proteomic Strep-tag system experiments followed by mass spectrometry analyses were performed. As a result of proteomic analysis, seven kinds of lectin-like molecules were identified, and we selected vesicular integral membrane protein gene VIP36 as a candidate of the cargo protein that interacts with the α1-6 fucosylation (core fucose) on N-glycan according to bibliographical consideration. Expectedly, the knockout of the VIP36 gene in HepG2 cells suppressed the secretion of AFP-L3 and other fucosylated proteins, such as fucosylated alpha-1 antitrypsin, into bile duct-like structures. We propose that VIP36 could be a cargo protein involved in the apical secretion of fucosylated proteins in HepG2 cells. MDPI 2023-04-11 /pmc/articles/PMC10138374/ /pubmed/37108200 http://dx.doi.org/10.3390/ijms24087037 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Muranaka, Mizuki
Takamatsu, Shinji
Ouchida, Tsunenori
Kanazawa, Yuri
Kondo, Jumpei
Nakagawa, Tsutomu
Egashira, Yuriko
Fukagawa, Koji
Gu, Jianguo
Okamoto, Toru
Kamada, Yoshihiro
Miyoshi, Eiji
Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title_full Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title_fullStr Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title_full_unstemmed Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title_short Vesicular Integral-Membrane Protein 36 Is Involved in the Selective Secretion of Fucosylated Proteins into Bile Duct-like Structures in HepG2 Cells
title_sort vesicular integral-membrane protein 36 is involved in the selective secretion of fucosylated proteins into bile duct-like structures in hepg2 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138374/
https://www.ncbi.nlm.nih.gov/pubmed/37108200
http://dx.doi.org/10.3390/ijms24087037
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