Desmoglein 3 and keratin 10 expressions are reduced by chronic exposure to cigarette smoke in human keratinised oral mucosa explants

被引:18
作者
Donetti, Elena [1 ]
Gualerzi, Alice [1 ]
Bedoni, Marzia [1 ,2 ]
Volpari, Tatiana [1 ]
Sciarabba, Michele [1 ]
Tartaglia, Gianluca [1 ]
Sforza, Chiarella [1 ]
机构
[1] Univ Milan, Dipartimento Morfol Umana & Sci Biomed Citta Stud, I-20133 Milan, Italy
[2] Fdn Don Carlo Gnocchi, I-20148 Milan, Italy
关键词
Intercellular junctions; Cytoskeleton; Electron microscopy; Fluorescence microscopy; Human oral keratinocytes; IN-VITRO; DESMOSOMAL CADHERINS; STRATUM-CORNEUM; GENE-EXPRESSION; TOBACCO-SMOKE; NICOTINE; CANCER; SKIN; DIFFERENTIATION; CARCINOGENESIS;
D O I
10.1016/j.archoralbio.2010.07.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Oral mucosa is a physiological barrier against several exogenous stimuli, among which cigarette smoke represents a source of reactive oxidizing compounds. No morphological evidences exist on the smoke effects induced in the human oral epithelium. In this study we performed a preliminary light and transmission electron microscopy morphological evaluation focussing in particular on keratinocyte intercellular adhesion and terminal differentiation in chronic smokers. Design: Human biopsies were obtained from healthy young chronic smoker women (n = 5) compared with a parallel group of non-smoker healthy volunteers (n = 5), as the smoking habit among women is ever more spreading. Samples were processed for light and transmission electron microscopy. On paraffin sections Masson's and Dane and Herman's histochemical staining were performed. Biomarker expressions of intercellular adhesion (desmoglein 3, Dsg3), terminal differentiation (keratin 10, K10 and keratin 14, K14), and basal membrane preservation (laminin) were investigated by immunofluorescence. Results: In both groups the epithelial structural integrity, homeostasis, and the basal membrane were comparable. Dsg3 and K10 expressions were affected in smokers with the former significantly reduced (p < 0.05). Ultrastructural analysis showed hypertrophic keratinocytes in the upper spinous layer and morphologically preserved desmosomes throughout the epithelial compartment. Conclusions: The reduction of Dsg3 and K10 expressions indicates that the overall process of keratinocyte terminal differentiation was altered. These preliminary results strongly suggest that Dsg3 and K10 can represent valuable immunomarkers to evaluate the tissue attempt to respond to an exogenous stress such as chronic cigarette smoke, but further samples need to be analysed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:815 / 823
页数:9
相关论文
共 42 条
[1]  
ADAMS D, 1976, ANN ROY COLL SURG, V58, P351
[2]  
ANDERSEN L, 1986, HUMAN ORAL EMBRYOLOG
[3]   Effects of Cigarette Smoke on the Human Oral Mucosal Transcriptome [J].
Boyle, Jay O. ;
Gumus, Zeynep H. ;
Kacker, Ashutosh ;
Choksi, Vishal L. ;
Bocker, Jennifer M. ;
Zhou, Xi Kathy ;
Yantiss, Rhonda K. ;
Hughes, Duncan B. ;
Du, Baoheng ;
Judson, Benjamin L. ;
Subbaramaiah, Kotha ;
Dannenberg, Andrew J. .
CANCER PREVENTION RESEARCH, 2010, 3 (03) :266-278
[4]   Structure and functions of keratin proteins in simple, stratified, keratinized and cornified epithelia [J].
Bragulla, Hermann H. ;
Homberger, Dominique G. .
JOURNAL OF ANATOMY, 2009, 214 (04) :516-559
[5]   Morphological alterations in the epithelium of the oral mucosa of rats (Rattus norvegicus) submitted to long-term systemic nicotine treatment [J].
Caldeira, Eduardo Jose ;
Fabrega Carvalho, Cesar Alexandre ;
Padovani, Carlos Roberto ;
Camilli, Jose Angelo ;
Garcia, Progresso Jose ;
Alves Cagnon, Valeria Helena .
ARCHIVES OF ORAL BIOLOGY, 2007, 52 (01) :83-89
[6]   DSG3 is overexpressed in head neck cancer and is a potential molecular target for inhibition of oncogenesis [J].
Chen, Y-J ;
Chang, J. T. ;
Lee, L. ;
Wang, H-M ;
Liao, C-T ;
Chiu, C-C ;
Chen, P-J ;
Cheng, A-J .
ONCOGENE, 2007, 26 (03) :467-476
[7]   A role for fibroblasts in mediating the effects of tobacco-induced epithelial cell growth and invasion [J].
Coppe, Jean-Philippe ;
Boysen, Megan ;
Sun, Chung Ho ;
Wong, Brian J. F. ;
Kang, Mo K. ;
Park, No-Hee ;
Desprez, Pierre-Yves ;
Campisi, Judith ;
Krtolica, Ana .
MOLECULAR CANCER RESEARCH, 2008, 6 (07) :1085-1098
[8]  
COSIO MG, 1980, AM REV RESPIR DIS, V122, P265
[9]   Protein carbonylation, cellular dysfunction, and disease progression [J].
Dalle-Donne, Isabella ;
Aldini, Giancarlo ;
Carini, Marina ;
Colombo, Roberto ;
Rossi, Ranieri ;
Milzani, Aldo .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2006, 10 (02) :389-406
[10]   An in vitro model of human oral explants to study early effects of radiation mucositis [J].
Donetti, Elena ;
Bedoni, Marzia ;
Capone, Paolo ;
Gualerzi, Alice ;
Tartaglia, Gianluca ;
Sforza, Chiarella .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2009, 117 (02) :169-174