author_facet Nagai, Koichi
Arai, Hideo
Okudera, Michisato
Yamamura, Takashi
Oki, Hidero
Komiyama, Kazuo
Nagai, Koichi
Arai, Hideo
Okudera, Michisato
Yamamura, Takashi
Oki, Hidero
Komiyama, Kazuo
author Nagai, Koichi
Arai, Hideo
Okudera, Michisato
Yamamura, Takashi
Oki, Hidero
Komiyama, Kazuo
spellingShingle Nagai, Koichi
Arai, Hideo
Okudera, Michisato
Yamamura, Takashi
Oki, Hidero
Komiyama, Kazuo
Journal of Oral Pathology & Medicine
Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
Periodontics
Cancer Research
Otorhinolaryngology
Oral Surgery
Pathology and Forensic Medicine
author_sort nagai, koichi
spelling Nagai, Koichi Arai, Hideo Okudera, Michisato Yamamura, Takashi Oki, Hidero Komiyama, Kazuo 0904-2512 1600-0714 Wiley Periodontics Cancer Research Otorhinolaryngology Oral Surgery Pathology and Forensic Medicine http://dx.doi.org/10.1111/jop.12145 <jats:p>Acinar cell regeneration from tubular structures has been reported to occur in duct‐deligated salivary glands. However, the detailed process of acinar cell regeneration has not been clarified. We have developed a mouse duct ligation model to clarify the mechanisms underlying acinar cell regeneration, and we analyzed the epidermal growth factor receptor (<jats:styled-content style="fixed-case">EGFR</jats:styled-content>) and epidermal growth factor (<jats:styled-content style="fixed-case">EGF</jats:styled-content>) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> methods. In the duct‐ligated portion of the submandibular gland (<jats:styled-content style="fixed-case">SMG</jats:styled-content>) that underwent atrophy, newly formed acinar cells were observed arising from the tubular structures after the release of the duct obstruction. The constitutive expression of <jats:styled-content style="fixed-case">EGFR</jats:styled-content> was observed by immunohistochemistry in both the duct‐ligated and duct‐deligated animals as well as in normal controls. The <jats:styled-content style="fixed-case">EGFR</jats:styled-content> phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> showed an increase in the epiregulin and heparin‐binding <jats:styled-content style="fixed-case">EGF</jats:styled-content> levels from day 0 to day 3 after the release of the duct obstruction. The <jats:styled-content style="fixed-case">EGF</jats:styled-content> level was increased only after day 7. <jats:italic>In vitro</jats:italic>, cultured cells isolated from ligated <jats:styled-content style="fixed-case">SMG</jats:styled-content>s proliferated and produced <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands following the addition of epiregulin to the culture medium. These findings suggest that the tubular structures localized in an atrophic gland are the source of acinar cell regeneration of the salivary gland. The induction of <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.</jats:p> Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model Journal of Oral Pathology & Medicine
doi_str_mv 10.1111/jop.12145
facet_avail Online
finc_class_facet Medizin
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTExMS9qb3AuMTIxNDU
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTExMS9qb3AuMTIxNDU
institution DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
DE-D161
imprint Wiley, 2014
imprint_str_mv Wiley, 2014
issn 0904-2512
1600-0714
issn_str_mv 0904-2512
1600-0714
language English
mega_collection Wiley (CrossRef)
match_str nagai2014epireguliniscriticalfortheacinarcellregenerationofthesubmandibularglandinamouseductligationmodel
publishDateSort 2014
publisher Wiley
recordtype ai
record_format ai
series Journal of Oral Pathology & Medicine
source_id 49
title Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_unstemmed Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_full Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_fullStr Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_full_unstemmed Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_short Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_sort epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
topic Periodontics
Cancer Research
Otorhinolaryngology
Oral Surgery
Pathology and Forensic Medicine
url http://dx.doi.org/10.1111/jop.12145
publishDate 2014
physical 378-387
description <jats:p>Acinar cell regeneration from tubular structures has been reported to occur in duct‐deligated salivary glands. However, the detailed process of acinar cell regeneration has not been clarified. We have developed a mouse duct ligation model to clarify the mechanisms underlying acinar cell regeneration, and we analyzed the epidermal growth factor receptor (<jats:styled-content style="fixed-case">EGFR</jats:styled-content>) and epidermal growth factor (<jats:styled-content style="fixed-case">EGF</jats:styled-content>) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> methods. In the duct‐ligated portion of the submandibular gland (<jats:styled-content style="fixed-case">SMG</jats:styled-content>) that underwent atrophy, newly formed acinar cells were observed arising from the tubular structures after the release of the duct obstruction. The constitutive expression of <jats:styled-content style="fixed-case">EGFR</jats:styled-content> was observed by immunohistochemistry in both the duct‐ligated and duct‐deligated animals as well as in normal controls. The <jats:styled-content style="fixed-case">EGFR</jats:styled-content> phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> showed an increase in the epiregulin and heparin‐binding <jats:styled-content style="fixed-case">EGF</jats:styled-content> levels from day 0 to day 3 after the release of the duct obstruction. The <jats:styled-content style="fixed-case">EGF</jats:styled-content> level was increased only after day 7. <jats:italic>In vitro</jats:italic>, cultured cells isolated from ligated <jats:styled-content style="fixed-case">SMG</jats:styled-content>s proliferated and produced <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands following the addition of epiregulin to the culture medium. These findings suggest that the tubular structures localized in an atrophic gland are the source of acinar cell regeneration of the salivary gland. The induction of <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.</jats:p>
container_issue 5
container_start_page 378
container_title Journal of Oral Pathology & Medicine
container_volume 43
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792348852566622224
geogr_code not assigned
last_indexed 2024-03-01T18:17:17.038Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Epiregulin+is+critical+for+the+acinar+cell+regeneration+of+the+submandibular+gland+in+a+mouse+duct+ligation+model&rft.date=2014-05-01&genre=article&issn=1600-0714&volume=43&issue=5&spage=378&epage=387&pages=378-387&jtitle=Journal+of+Oral+Pathology+%26+Medicine&atitle=Epiregulin+is+critical+for+the+acinar+cell+regeneration+of+the+submandibular+gland+in+a+mouse+duct+ligation+model&aulast=Komiyama&aufirst=Kazuo&rft_id=info%3Adoi%2F10.1111%2Fjop.12145&rft.language%5B0%5D=eng
SOLR
_version_ 1792348852566622224
author Nagai, Koichi, Arai, Hideo, Okudera, Michisato, Yamamura, Takashi, Oki, Hidero, Komiyama, Kazuo
author_facet Nagai, Koichi, Arai, Hideo, Okudera, Michisato, Yamamura, Takashi, Oki, Hidero, Komiyama, Kazuo, Nagai, Koichi, Arai, Hideo, Okudera, Michisato, Yamamura, Takashi, Oki, Hidero, Komiyama, Kazuo
author_sort nagai, koichi
container_issue 5
container_start_page 378
container_title Journal of Oral Pathology & Medicine
container_volume 43
description <jats:p>Acinar cell regeneration from tubular structures has been reported to occur in duct‐deligated salivary glands. However, the detailed process of acinar cell regeneration has not been clarified. We have developed a mouse duct ligation model to clarify the mechanisms underlying acinar cell regeneration, and we analyzed the epidermal growth factor receptor (<jats:styled-content style="fixed-case">EGFR</jats:styled-content>) and epidermal growth factor (<jats:styled-content style="fixed-case">EGF</jats:styled-content>) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> methods. In the duct‐ligated portion of the submandibular gland (<jats:styled-content style="fixed-case">SMG</jats:styled-content>) that underwent atrophy, newly formed acinar cells were observed arising from the tubular structures after the release of the duct obstruction. The constitutive expression of <jats:styled-content style="fixed-case">EGFR</jats:styled-content> was observed by immunohistochemistry in both the duct‐ligated and duct‐deligated animals as well as in normal controls. The <jats:styled-content style="fixed-case">EGFR</jats:styled-content> phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> showed an increase in the epiregulin and heparin‐binding <jats:styled-content style="fixed-case">EGF</jats:styled-content> levels from day 0 to day 3 after the release of the duct obstruction. The <jats:styled-content style="fixed-case">EGF</jats:styled-content> level was increased only after day 7. <jats:italic>In vitro</jats:italic>, cultured cells isolated from ligated <jats:styled-content style="fixed-case">SMG</jats:styled-content>s proliferated and produced <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands following the addition of epiregulin to the culture medium. These findings suggest that the tubular structures localized in an atrophic gland are the source of acinar cell regeneration of the salivary gland. The induction of <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.</jats:p>
doi_str_mv 10.1111/jop.12145
facet_avail Online
finc_class_facet Medizin
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTExMS9qb3AuMTIxNDU
imprint Wiley, 2014
imprint_str_mv Wiley, 2014
institution DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161
issn 0904-2512, 1600-0714
issn_str_mv 0904-2512, 1600-0714
language English
last_indexed 2024-03-01T18:17:17.038Z
match_str nagai2014epireguliniscriticalfortheacinarcellregenerationofthesubmandibularglandinamouseductligationmodel
mega_collection Wiley (CrossRef)
physical 378-387
publishDate 2014
publishDateSort 2014
publisher Wiley
record_format ai
recordtype ai
series Journal of Oral Pathology & Medicine
source_id 49
spelling Nagai, Koichi Arai, Hideo Okudera, Michisato Yamamura, Takashi Oki, Hidero Komiyama, Kazuo 0904-2512 1600-0714 Wiley Periodontics Cancer Research Otorhinolaryngology Oral Surgery Pathology and Forensic Medicine http://dx.doi.org/10.1111/jop.12145 <jats:p>Acinar cell regeneration from tubular structures has been reported to occur in duct‐deligated salivary glands. However, the detailed process of acinar cell regeneration has not been clarified. We have developed a mouse duct ligation model to clarify the mechanisms underlying acinar cell regeneration, and we analyzed the epidermal growth factor receptor (<jats:styled-content style="fixed-case">EGFR</jats:styled-content>) and epidermal growth factor (<jats:styled-content style="fixed-case">EGF</jats:styled-content>) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> methods. In the duct‐ligated portion of the submandibular gland (<jats:styled-content style="fixed-case">SMG</jats:styled-content>) that underwent atrophy, newly formed acinar cells were observed arising from the tubular structures after the release of the duct obstruction. The constitutive expression of <jats:styled-content style="fixed-case">EGFR</jats:styled-content> was observed by immunohistochemistry in both the duct‐ligated and duct‐deligated animals as well as in normal controls. The <jats:styled-content style="fixed-case">EGFR</jats:styled-content> phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. <jats:styled-content style="fixed-case">RT</jats:styled-content>‐<jats:styled-content style="fixed-case">PCR</jats:styled-content> showed an increase in the epiregulin and heparin‐binding <jats:styled-content style="fixed-case">EGF</jats:styled-content> levels from day 0 to day 3 after the release of the duct obstruction. The <jats:styled-content style="fixed-case">EGF</jats:styled-content> level was increased only after day 7. <jats:italic>In vitro</jats:italic>, cultured cells isolated from ligated <jats:styled-content style="fixed-case">SMG</jats:styled-content>s proliferated and produced <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands following the addition of epiregulin to the culture medium. These findings suggest that the tubular structures localized in an atrophic gland are the source of acinar cell regeneration of the salivary gland. The induction of <jats:styled-content style="fixed-case">EGF</jats:styled-content> ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.</jats:p> Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model Journal of Oral Pathology & Medicine
spellingShingle Nagai, Koichi, Arai, Hideo, Okudera, Michisato, Yamamura, Takashi, Oki, Hidero, Komiyama, Kazuo, Journal of Oral Pathology & Medicine, Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model, Periodontics, Cancer Research, Otorhinolaryngology, Oral Surgery, Pathology and Forensic Medicine
title Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_full Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_fullStr Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_full_unstemmed Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_short Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_sort epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
title_unstemmed Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model
topic Periodontics, Cancer Research, Otorhinolaryngology, Oral Surgery, Pathology and Forensic Medicine
url http://dx.doi.org/10.1111/jop.12145