Cargando…

Degradation of MUC7 and MUC5B in Human Saliva

BACKGROUND: Two types of mucins, MUC7 and MUC5B constitute the major salivary glycoproteins, however their metabolic turnover has not been elucidated in detail to date. This study was conducted to examine turnover of MUC7 and MUC5B in saliva, by focusing on the relationship between their deglycosyla...

Descripción completa

Detalles Bibliográficos
Autores principales: Takehara, Sachiko, Yanagishita, Masaki, Podyma-Inoue, Katarzyna Anna, Kawaguchi, Yoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715446/
https://www.ncbi.nlm.nih.gov/pubmed/23874867
http://dx.doi.org/10.1371/journal.pone.0069059
_version_ 1782277456092200960
author Takehara, Sachiko
Yanagishita, Masaki
Podyma-Inoue, Katarzyna Anna
Kawaguchi, Yoko
author_facet Takehara, Sachiko
Yanagishita, Masaki
Podyma-Inoue, Katarzyna Anna
Kawaguchi, Yoko
author_sort Takehara, Sachiko
collection PubMed
description BACKGROUND: Two types of mucins, MUC7 and MUC5B constitute the major salivary glycoproteins, however their metabolic turnover has not been elucidated in detail to date. This study was conducted to examine turnover of MUC7 and MUC5B in saliva, by focusing on the relationship between their deglycosylation and proteolysis. METHODOLOGY/PRINCIPAL FINDINGS: Whole saliva samples were collected from healthy individuals and incubated at 37°C in the presence of various protease inhibitors, sialidase, or a sialidase inhibitor. General degradation patterns of salivary proteins and glycoproteins were examined by SDS-polyacrylamide-gel-electrophoresis. Furthermore, changes of molecular sizes of MUC7 and MUC5B were examined by Western blot analysis. A protein band was identified as MUC7 by Western blot analysis using an antibody recognizing an N-terminal epitope. The MUC7 signal disappeared rapidly after 20-minutes of incubation. In contrast, the band of MUC7 stained for its carbohydrate components remained visible near its original position for a longer time indicating that the rapid loss of Western blot signal was due to the specific removal of the N-termimal epitope. Pretreatment of saliva with sialidase facilitated MUC7 protein degradation when compared with samples without treatment. Furthermore, addition of sialidase inhibitor to saliva prevented proteolysis of N-terminus of MUC7, suggesting that the desialylation is a prerequisite for the degradation of the N-terminal region of MUC7. The protein band corresponding to MUC5B detected in both Western blotting and glycoprotein staining showed little sign of significant degradation upon incubation in saliva up to 9 hours. CONCLUSIONS/SIGNIFICANCE: MUC7 was highly susceptible to specific proteolysis in saliva, though major part of MUC5B was more resistant to degradation. The N-terminal region of MUC7, particularly sensitive to proteolytic degradation, has also been proposed to have distinct biological function such as antibacterial activities. Quick removal of this region may have biologically important implication.
format Online
Article
Text
id pubmed-3715446
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37154462013-07-19 Degradation of MUC7 and MUC5B in Human Saliva Takehara, Sachiko Yanagishita, Masaki Podyma-Inoue, Katarzyna Anna Kawaguchi, Yoko PLoS One Research Article BACKGROUND: Two types of mucins, MUC7 and MUC5B constitute the major salivary glycoproteins, however their metabolic turnover has not been elucidated in detail to date. This study was conducted to examine turnover of MUC7 and MUC5B in saliva, by focusing on the relationship between their deglycosylation and proteolysis. METHODOLOGY/PRINCIPAL FINDINGS: Whole saliva samples were collected from healthy individuals and incubated at 37°C in the presence of various protease inhibitors, sialidase, or a sialidase inhibitor. General degradation patterns of salivary proteins and glycoproteins were examined by SDS-polyacrylamide-gel-electrophoresis. Furthermore, changes of molecular sizes of MUC7 and MUC5B were examined by Western blot analysis. A protein band was identified as MUC7 by Western blot analysis using an antibody recognizing an N-terminal epitope. The MUC7 signal disappeared rapidly after 20-minutes of incubation. In contrast, the band of MUC7 stained for its carbohydrate components remained visible near its original position for a longer time indicating that the rapid loss of Western blot signal was due to the specific removal of the N-termimal epitope. Pretreatment of saliva with sialidase facilitated MUC7 protein degradation when compared with samples without treatment. Furthermore, addition of sialidase inhibitor to saliva prevented proteolysis of N-terminus of MUC7, suggesting that the desialylation is a prerequisite for the degradation of the N-terminal region of MUC7. The protein band corresponding to MUC5B detected in both Western blotting and glycoprotein staining showed little sign of significant degradation upon incubation in saliva up to 9 hours. CONCLUSIONS/SIGNIFICANCE: MUC7 was highly susceptible to specific proteolysis in saliva, though major part of MUC5B was more resistant to degradation. The N-terminal region of MUC7, particularly sensitive to proteolytic degradation, has also been proposed to have distinct biological function such as antibacterial activities. Quick removal of this region may have biologically important implication. Public Library of Science 2013-07-18 /pmc/articles/PMC3715446/ /pubmed/23874867 http://dx.doi.org/10.1371/journal.pone.0069059 Text en © 2013 Takehara 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Takehara, Sachiko
Yanagishita, Masaki
Podyma-Inoue, Katarzyna Anna
Kawaguchi, Yoko
Degradation of MUC7 and MUC5B in Human Saliva
title Degradation of MUC7 and MUC5B in Human Saliva
title_full Degradation of MUC7 and MUC5B in Human Saliva
title_fullStr Degradation of MUC7 and MUC5B in Human Saliva
title_full_unstemmed Degradation of MUC7 and MUC5B in Human Saliva
title_short Degradation of MUC7 and MUC5B in Human Saliva
title_sort degradation of muc7 and muc5b in human saliva
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715446/
https://www.ncbi.nlm.nih.gov/pubmed/23874867
http://dx.doi.org/10.1371/journal.pone.0069059
work_keys_str_mv AT takeharasachiko degradationofmuc7andmuc5binhumansaliva
AT yanagishitamasaki degradationofmuc7andmuc5binhumansaliva
AT podymainouekatarzynaanna degradationofmuc7andmuc5binhumansaliva
AT kawaguchiyoko degradationofmuc7andmuc5binhumansaliva