Literature DB >> 24354788

Epiregulin is critical for the acinar cell regeneration of the submandibular gland in a mouse duct ligation model.

Koichi Nagai1, Hideo Arai, Michisato Okudera, Takashi Yamamura, Hidero Oki, Kazuo Komiyama.   

Abstract

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 (EGFR) and epidermal growth factor (EGF) ligands using the model. We studied these ligands expressions in the course of acinar cell regeneration using immunohistochemistry and RT-PCR methods. In the duct-ligated portion of the submandibular gland (SMG) 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 EGFR was observed by immunohistochemistry in both the duct-ligated and duct-deligated animals as well as in normal controls. The EGFR phosphorylation detected on the tubular structures after duct ligation paralleled the acinar cell regeneration. RT-PCR showed an increase in the epiregulin and heparin-binding EGF levels from day 0 to day 3 after the release of the duct obstruction. The EGF level was increased only after day 7. In vitro, cultured cells isolated from ligated SMGs proliferated and produced EGF 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 EGF ligands, in particular epiregulin, may play an important role in acinar cell regeneration in this model.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  acinar cell; duct obstruction; epiregulin; hyposalivation; mouse; submandibular gland

Mesh:

Substances:

Year:  2013        PMID: 24354788     DOI: 10.1111/jop.12145

Source DB:  PubMed          Journal:  J Oral Pathol Med        ISSN: 0904-2512            Impact factor:   4.253


  8 in total

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2.  Epithelial Cell Lineage and Signaling in Murine Salivary Glands.

Authors:  M H Aure; J M Symonds; J W Mays; M P Hoffman
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Journal:  Cell Mol Biol Lett       Date:  2022-06-11       Impact factor: 8.702

4.  Alteration in cellular turnover and progenitor cell population in lacrimal glands from thrombospondin 1-/- mice, a model of dry eye.

Authors:  Marie A Shatos; Robin R Hodges; Masahiro Morinaga; David E McNay; Rakibul Islam; Sumit Bhattacharya; Dayu Li; Bruce Turpie; Helen P Makarenkova; Sharmila Masli; Tor P Utheim; Darlene A Dartt
Journal:  Exp Eye Res       Date:  2016-09-30       Impact factor: 3.467

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Journal:  Development       Date:  2016-03-17       Impact factor: 6.868

Review 6.  EGF receptor ligands: recent advances.

Authors:  Bhuminder Singh; Graham Carpenter; Robert J Coffey
Journal:  F1000Res       Date:  2016-09-08

7.  Expression of c-kit and Cytokeratin 5 in the Submandibular Gland after Release of Long-Term Ligation of the Main Excretory Duct in Mice.

Authors:  Hiroshi Watanabe; Haruka Takahashi; Miyuki Hata-Kawakami; Akira Tanaka
Journal:  Acta Histochem Cytochem       Date:  2017-06-22       Impact factor: 1.938

Review 8.  Experimental Animal Model Systems for Understanding Salivary Secretory Disorders.

Authors:  Ji-Youn Kim; Chang-Hyeon An; Jae-Young Kim; Jae-Kwang Jung
Journal:  Int J Mol Sci       Date:  2020-11-10       Impact factor: 5.923

  8 in total

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