Immunohistological characterization of myoepithelial cells using monoclonal antibodies

Aim: The aim of this study was to investigate the expression of monoclonal antibody (mAbs) in the myoepithelial cells of the rat submandibular salivary glands (SSG) during postnatal development. Material and method: SSG were obtained from 1, 30 and 60 days old, male, AO rats. Streptavidin-biotin imm...

Full description

Bibliographic Details
Main Authors: Dožić Ivan, Čolić Miodrag
Format: Article
Language:English
Published: Serbian Medical Society - Dental Section, Belgrade 2008-01-01
Series:Stomatološki glasnik Srbije
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0039-1743/2008/0039-17430801007D.pdf
id doaj-57069b24ee354bd7a9e3852792530951
record_format Article
spelling doaj-57069b24ee354bd7a9e38527925309512020-11-24T21:02:20ZengSerbian Medical Society - Dental Section, BelgradeStomatološki glasnik Srbije0039-17432008-01-0155171410.2298/SGS0801007DImmunohistological characterization of myoepithelial cells using monoclonal antibodiesDožić IvanČolić MiodragAim: The aim of this study was to investigate the expression of monoclonal antibody (mAbs) in the myoepithelial cells of the rat submandibular salivary glands (SSG) during postnatal development. Material and method: SSG were obtained from 1, 30 and 60 days old, male, AO rats. Streptavidin-biotin immunoperoxidase method was used for immunohistochemistry. Cryostat sections were fixed in acetone and incubated with mAbs which specifically reacts with cytokeratins (CK) polypeptides ( CK7, CK8, CK18, CK kidney, K8.12, K8.13), rats epithelial (PT13D11), rats collagen (RMC-23), laminin (α6β1) and rats sialoadhesin (ED3). Results: Immunohistochemical analysis of the myoepithelial cells showed phenotypic heterogeneity during the postnatal development. Myoepithelial cells of acini were stained by K8.13, PT13D11 and ED3 mAbs, whereas these cells were not stained by mAbs CK7, CK8, CK18, CK-kidney, RMC-23 and α6β1. In adult rats, myoepithelial cells of excretory duct were stained by K8.12 mAb. Conclusion: The obtained results show phenotypic heterogeneity of myoepithelial cells and might also be useful to further understanding of myoepithelial cells development and functions. http://www.doiserbia.nb.rs/img/doi/0039-1743/2008/0039-17430801007D.pdfmyoepithelial cellssubmandibular salivary glandsmonoclonal antibodyontogenesis
collection DOAJ
language English
format Article
sources DOAJ
author Dožić Ivan
Čolić Miodrag
spellingShingle Dožić Ivan
Čolić Miodrag
Immunohistological characterization of myoepithelial cells using monoclonal antibodies
Stomatološki glasnik Srbije
myoepithelial cells
submandibular salivary glands
monoclonal antibody
ontogenesis
author_facet Dožić Ivan
Čolić Miodrag
author_sort Dožić Ivan
title Immunohistological characterization of myoepithelial cells using monoclonal antibodies
title_short Immunohistological characterization of myoepithelial cells using monoclonal antibodies
title_full Immunohistological characterization of myoepithelial cells using monoclonal antibodies
title_fullStr Immunohistological characterization of myoepithelial cells using monoclonal antibodies
title_full_unstemmed Immunohistological characterization of myoepithelial cells using monoclonal antibodies
title_sort immunohistological characterization of myoepithelial cells using monoclonal antibodies
publisher Serbian Medical Society - Dental Section, Belgrade
series Stomatološki glasnik Srbije
issn 0039-1743
publishDate 2008-01-01
description Aim: The aim of this study was to investigate the expression of monoclonal antibody (mAbs) in the myoepithelial cells of the rat submandibular salivary glands (SSG) during postnatal development. Material and method: SSG were obtained from 1, 30 and 60 days old, male, AO rats. Streptavidin-biotin immunoperoxidase method was used for immunohistochemistry. Cryostat sections were fixed in acetone and incubated with mAbs which specifically reacts with cytokeratins (CK) polypeptides ( CK7, CK8, CK18, CK kidney, K8.12, K8.13), rats epithelial (PT13D11), rats collagen (RMC-23), laminin (α6β1) and rats sialoadhesin (ED3). Results: Immunohistochemical analysis of the myoepithelial cells showed phenotypic heterogeneity during the postnatal development. Myoepithelial cells of acini were stained by K8.13, PT13D11 and ED3 mAbs, whereas these cells were not stained by mAbs CK7, CK8, CK18, CK-kidney, RMC-23 and α6β1. In adult rats, myoepithelial cells of excretory duct were stained by K8.12 mAb. Conclusion: The obtained results show phenotypic heterogeneity of myoepithelial cells and might also be useful to further understanding of myoepithelial cells development and functions.
topic myoepithelial cells
submandibular salivary glands
monoclonal antibody
ontogenesis
url http://www.doiserbia.nb.rs/img/doi/0039-1743/2008/0039-17430801007D.pdf
work_keys_str_mv AT dozicivan immunohistologicalcharacterizationofmyoepithelialcellsusingmonoclonalantibodies
AT colicmiodrag immunohistologicalcharacterizationofmyoepithelialcellsusingmonoclonalantibodies
_version_ 1716775675221770240