Electron microscopic detection of salivary α-amylase in the pellicle formed in situ

被引:43
作者
Deimling, D
Breschi, L
Hoth-Hannig, W
Ruggeri, A
Hannig, C
Nekrashevych, Y
Prati, C
Hannig, M
机构
[1] Univ Freiburg, Dept Operat Dent & Periodontol, D-79106 Freiburg, Germany
[2] Univ Trieste, Dept Surg Sci, Trieste, Italy
[3] Univ Saarland, Dept Operat Dent & Periodontol, D-6650 Homburg, Germany
[4] Univ Bologna, Dept SAU & FAL, Bologna, Italy
[5] Univ Gottingen, Dept Operat & Prevent Dent, D-3400 Gottingen, Germany
[6] Univ Bologna, Dept Dent Sci, Bologna, Italy
关键词
alpha-amylase; FEI-SEM; immunogold-labeling; salivary pellicle; TEM;
D O I
10.1111/j.1600-0722.2004.00168.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Immunological and biochemical analyses have shown that alpha-amylase is an essential component of the acquired pellicle. After adsorption, this enzyme might act as a receptor for bacterial adherence. However, data indicating that amylase is bound to the pellicle surface in vivo and thus available for adhering bacteria are rare. Therefore, the present study focused on alpha-amylase within the pellicle formed in situ, using gold-immunolabeling electron microscopic techniques. Pellicles were formed by intra-oral exposure of enamel specimens for 30 and 120 min in six subjects. The results obtained by transmission electron microscopy indicate that amylase was randomly distributed in the pellicle layer without any preferential localization within the pellicle. Thus, salivary alpha-amylase might be considered as an important structural component that is even involved in the early stages of pellicle formation. The findings of field emission in-lens scanning electron microscopy provided evidence that the enzyme is located on the pellicle surface. It could be concluded that alpha-amylase might act as a receptor for bacterial adherence to the pellicle in vivo.
引用
收藏
页码:503 / 509
页数:7
相关论文
共 25 条
[1]   CHARACTERIZATION OF INVIVO SALIVARY-DERIVED ENAMEL PELLICLE [J].
ALHASHIMI, I ;
LEVINE, MJ .
ARCHIVES OF ORAL BIOLOGY, 1989, 34 (04) :289-295
[2]   Thickness of acquired salivary pellicle as a determinant of the sites of dental erosion [J].
Amaechi, BT ;
Higham, SM ;
Edgar, WM ;
Milosevic, A .
JOURNAL OF DENTAL RESEARCH, 1999, 78 (12) :1821-1828
[3]   Dentin proteoglycans: An immunocytochemical FEISEM study [J].
Breschi, L ;
Lopes, M ;
Gobbi, P ;
Mazzotti, G ;
Falconi, M ;
Perdigao, J .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 61 (01) :40-46
[4]   Composition of pellicles formed in vivo on tooth surfaces in different parts of the dentition, and in vitro on hydroxyapatite [J].
Carlén, A ;
Börjesson, AC ;
Nikdel, K ;
Olsson, J .
CARIES RESEARCH, 1998, 32 (06) :447-455
[5]  
CLASEN ABS, 2000, TOOTH WEAR SENSITIVI, P189
[6]   ROLE OF HYDROPHOBIC AND HYDROPHILIC FORCES IN PEPTIDE-PROTEIN INTERACTION - NEW ADVANCES [J].
CSERHATI, T ;
SZOGYI, M .
PEPTIDES, 1995, 16 (01) :165-173
[7]  
Douglas C W, 1994, Adv Dent Res, V8, P254
[8]   THE BINDING OF HUMAN SALIVARY ALPHA-AMYLASE BY ORAL STRAINS OF STREPTOCOCCAL BACTERIA [J].
DOUGLAS, CWI .
ARCHIVES OF ORAL BIOLOGY, 1983, 28 (07) :567-573
[9]   CHARACTERIZATION OF THE ALPHA-AMYLASE RECEPTOR OF STREPTOCOCCUS-GORDONII NCTC-7868 [J].
DOUGLAS, CWI .
JOURNAL OF DENTAL RESEARCH, 1990, 69 (11) :1746-1752
[10]   CHARACTERIZATION OF ACQUIRED DENTURE PELLICLE FROM HEALTHY AND STOMATITIS PATIENTS [J].
EDGERTON, M ;
LEVINE, MJ .
JOURNAL OF PROSTHETIC DENTISTRY, 1992, 68 (04) :683-691