Morphological evaluation of tongue mucosa in burning mouth syndrome

被引:18
作者
Sardella, Andrea [1 ]
Gualerzi, Alice [2 ]
Lodi, Giovanni [1 ]
Sforza, Chiarella [2 ]
Carrassi, Antonio [1 ]
Donetti, Elena [2 ]
机构
[1] Univ Milan, Dipartimento Med Chirurg & Odontoiatria, Unita Med Orate Patol Orale & Odontoiatria Geriat, I-20122 Milan, Italy
[2] Univ Milan, Dipartimento Morfol Umana & Sci Biomed, Citta Studi, Italy
关键词
Burning mouth syndrome; Keratin; 16; Desmosomal cadherins; Occludin; EXPRESSION; KERATINS; STIMULATION; RECEPTORS; PAIN;
D O I
10.1016/j.archoralbio.2011.07.007
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: The aim of the present study was to perform a morphological evaluation by immunofluorescence of biomarkers of keratinocyte intercellular adhesion, and of differentiation in the tongue mucosa of burning mouth syndrome patients (BMS), compared with a control group. Design: A prospective blinded evaluation of tongue mucosal specimens processed for light microscopy was performed. Intercellular adhesion was evaluated by investigating the expression of desmoglein 1, desmoglein 3, and of occludin. Keratin 10 and keratin 14 (markers of epithelial differentiation) were also evaluated, as keratin 16 (marker for activated keratinocytes after epithelial injury). Apoptotic cascade was investigated by p53 and activated caspase-3 expression. The basal membrane integrity was analysed through laminin immunoreactivity. Results: In both groups, a preserved three-dimensional architecture of the tongue was observed. Desmoglein 1 and desmoglein 3 epithelial distributions were similar in the desmosomes of patients and control subjects. Again, keratin 10 immunoreactivity and distribution pattern of keratin 14 in the epithelial compartment was similar in both groups. In control samples, keratin 16 immunoreactivity was scant throughout the epithelium with a punctuate and scattered cytoplasmic labelling. In contrast, in all BMS patients keratinocyte cytoplasm was homogeneously labelled for keratin 16, with a more intense staining than controls. Furthermore, keratin 16 staining progressively decreased proceeding towards the most superficial epithelial layers. Conclusions: The results of this study are consistent with and support the clinically normal features of oral mucosa in BMS, and suggest that keratin 16 may be involved in the cell mechanisms underlying the syndrome occurrence. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 101
页数:8
相关论文
共 38 条
[31]   Expression of intermediate filament proteins in benign lesions of the oral mucosa [J].
van der Velden, LA ;
Manni, JJ ;
Ramaekers, FCS ;
Kuijpers, W .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 1999, 256 (10) :514-519
[32]   Exfoliative cytology of the oral mucosa in burning mouth syndrome: a cytomorphological and cytomorphometric analysis [J].
Wandeur, Talita ;
Bezerra de Moura, Sergio Adriane ;
Costa de Medeiros, Ana Miryam ;
Naval Machado, Maria Angela ;
de Azevedo Alanis, Luciana Reis ;
Trindade Gregio, Ana Maria ;
Trevilatto, Paula Cristina ;
Soares de Lima, Antonio Adilson .
GERODONTOLOGY, 2011, 28 (01) :44-48
[33]  
Woda A, 2009, J OROFAC PAIN, V20, P2
[34]   Effects of antikeratin 16 antibodies on the expression of Toll-like receptors 2 and 4 in keratinocytes [J].
Wu, C. ;
Luan, Q. ;
Li, C. ;
Zheng, Z. .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2009, 34 (02) :236-239
[35]   Burning mouth syndrome as a trigeminal small fibre neuropathy: Increased heat and capsaicin. receptor TRPV1 in nerve fibres correlates with pain score [J].
Yilmaz, Z. ;
Renton, T. ;
Yiangou, Y. ;
Zakrzewska, J. ;
Chessell, I. P. ;
Bountra, C. ;
Anand, P. .
JOURNAL OF CLINICAL NEUROSCIENCE, 2007, 14 (09) :864-871
[36]  
Zakrzewska JM, 1999, EPIDEMIOLOGY PAIN SE
[37]  
ZAKRZEWSKA JM, 2005, COCHRANE DB SYST REV, V25
[38]  
Zakrzewska Joanna M, 2009, Curr Opin Support Palliat Care, V3, P125, DOI 10.1097/SPC.0b013e32832b7d75