Immunoelectron Microscopic Study of Podoplanin Localization in Mouse Salivary Gland Myoepithelium
Identifieur interne : 005901 ( Main/Merge ); précédent : 005900; suivant : 005902Immunoelectron Microscopic Study of Podoplanin Localization in Mouse Salivary Gland Myoepithelium
Auteurs : Minoru Hata ; Ikuko Amano ; Eichi Tsuruga [Japon] ; Hiroshi Kojima ; Yoshihiko Sawa [Japon]Source :
- Acta Histochemica et Cytochemica [ 0044-5991 ] ; 2010.
Abstract
We have recently reported that salivary gland cells express the lymphatic endothelial cell marker podoplanin. The present study was aimed to immunohistochemically investigate the expression of the myoepithelial cell marker α-smooth muscle actin (SMA) on podoplanin-positive cells in mouse parotid and sublingual glands, and to elucidate podoplanin localization in salivary gland myoepithelial cells by immunoelectron microscopic study. The distribution of myoepithelial cells expressing podoplanin and α-SMA was examined by immunofluorescent staining, and the localization of reaction products of anti-podoplanin antibody was investigated by pre-embedded immunoelectron microscopic method. In immunohistochemistry, the surfaces of both the mucous acini terminal portion and ducts were covered by a number of extensive myoepithelial cellular processes expressing podoplanin, and the immunostaining level with anti-podoplanin antibody to myoepithelial cells completely coincided with the immunostaining level with anti-α-SMA antibody. These findings suggest that podoplanin is a salivary gland myoepithelial cell antigen, and that the detection level directly reflects the myoepithelial cell distribution. In immunoelectron microscopic study, a number of reaction products with anti-podoplanin antibody were found at the Golgi apparatus binding to the endoplasmic reticulum in the cytoplasm of myoepithelial cells between sublingual gland acinar cells, and were also found at the myoepithelial cell membrane. These findings suggest that salivary gland myoepithelial cells constantly produce podoplanin and glycosylate at the Golgi apparatus, and transport them to the cell membrane. Podoplanin may be involved in maintaining the homeostasis of myoepithelial cells through its characteristic as a mucin-type transmembrane glycoprotein.
Url:
DOI: 10.1267/ahc.10011
PubMed: 20514295
PubMed Central: 2875856
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Fukuoka Dental College</nlm:aff><wicri:noCountry code="subfield">Fukuoka Dental College</wicri:noCountry></affiliation></author><author><name sortKey="Tsuruga, Eichi" sort="Tsuruga, Eichi" uniqKey="Tsuruga E" first="Eichi" last="Tsuruga">Eichi Tsuruga</name><affiliation wicri:level="1"><nlm:aff id="aff2">Department of Morphological Biology, Fukuoka Dental College, 2–15–1 Tamura, Sawara-ku, Fukuoka 814–0193, Japan</nlm:aff><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Morphological Biology, Fukuoka Dental College, 2–15–1 Tamura, Sawara-ku, Fukuoka 814–0193</wicri:regionArea><wicri:noRegion>Fukuoka 814–0193</wicri:noRegion></affiliation></author><author><name sortKey="Kojima, Hiroshi" sort="Kojima, Hiroshi" uniqKey="Kojima H" first="Hiroshi" last="Kojima">Hiroshi Kojima</name><affiliation><nlm:aff id="aff1">Department of Oral Growth & Development, Fukuoka Dental College</nlm:aff><wicri:noCountry code="subfield">Fukuoka Dental College</wicri:noCountry></affiliation></author><author><name sortKey="Sawa, Yoshihiko" sort="Sawa, Yoshihiko" uniqKey="Sawa Y" first="Yoshihiko" last="Sawa">Yoshihiko Sawa</name><affiliation wicri:level="1"><nlm:aff id="aff2">Department of Morphological Biology, Fukuoka Dental College, 2–15–1 Tamura, Sawara-ku, Fukuoka 814–0193, Japan</nlm:aff><country xml:lang="fr">Japon</country><wicri:regionArea>Department of Morphological Biology, Fukuoka Dental College, 2–15–1 Tamura, Sawara-ku, Fukuoka 814–0193</wicri:regionArea><wicri:noRegion>Fukuoka 814–0193</wicri:noRegion></affiliation></author></analytic><series><title level="j">Acta Histochemica et Cytochemica</title><idno type="ISSN">0044-5991</idno><idno type="eISSN">1347-5800</idno><imprint><date when="2010">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>We have recently reported that salivary gland cells express the lymphatic endothelial cell marker podoplanin. The present study was aimed to immunohistochemically investigate the expression of the myoepithelial cell marker α-smooth muscle actin (SMA) on podoplanin-positive cells in mouse parotid and sublingual glands, and to elucidate podoplanin localization in salivary gland myoepithelial cells by immunoelectron microscopic study. The distribution of myoepithelial cells expressing podoplanin and α-SMA was examined by immunofluorescent staining, and the localization of reaction products of anti-podoplanin antibody was investigated by pre-embedded immunoelectron microscopic method. In immunohistochemistry, the surfaces of both the mucous acini terminal portion and ducts were covered by a number of extensive myoepithelial cellular processes expressing podoplanin, and the immunostaining level with anti-podoplanin antibody to myoepithelial cells completely coincided with the immunostaining level with anti-α-SMA antibody. These findings suggest that podoplanin is a salivary gland myoepithelial cell antigen, and that the detection level directly reflects the myoepithelial cell distribution. In immunoelectron microscopic study, a number of reaction products with anti-podoplanin antibody were found at the Golgi apparatus binding to the endoplasmic reticulum in the cytoplasm of myoepithelial cells between sublingual gland acinar cells, and were also found at the myoepithelial cell membrane. These findings suggest that salivary gland myoepithelial cells constantly produce podoplanin and glycosylate at the Golgi apparatus, and transport them to the cell membrane. Podoplanin may be involved in maintaining the homeostasis of myoepithelial cells through its characteristic as a mucin-type transmembrane glycoprotein.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Bocker, W" uniqKey="Bocker W">W. 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Hild</name></author><author><name sortKey="Brehm, R" uniqKey="Brehm R">R. Brehm</name></author><author><name sortKey="Steger, K" uniqKey="Steger K">K. Steger</name></author></analytic></biblStruct></listBibl></div1></back></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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