Langerin+ versus CD1a+ Langerhans cells in human gingival tissue:: a comparative and quantitative immunohistochemical study

被引:18
|
作者
Séguier, S
Bodineau, A
Godeau, G
Pellat, B
Brousse, N
机构
[1] Hop Necker Enfants Malad, Serv Anat & Cytol Pathol, F-75743 Paris 15, France
[2] Univ Paris 05, Fac Chirurg Dent, Dept Anat Pathol & Physiopathol Tissus Mineralise, F-92120 Montrouge, France
关键词
CD1a; Langerin; Langerhans cells; gingiva;
D O I
10.1016/S0003-9969(02)00173-5
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Langerhans cells (LC) are dendritic cells of the immune system able to capture intraepithelial pathogens and migrate to regional lymph nodes to present them to naive T cells. Up to now immunohistological. studies on human gingival LC have been carried out using antibodies against HLA-DR or CD1a molecules. A new marker of LC called Langerin (CD207) and described, among other subcellular localisations, in the Birbeck granules is now available in immunohistochemistry. The purpose of this in situ study was to quantify and to compare Langerin+ versus CD1a+ LC number in order to show differences in the expression of these molecules, if any, and to determine which marker is the most specific. The present study was conducted using nine frozen healthy gingival. samples. Double immunofluorescence procedures were performed with an anti-Langerin antibody revealed by FITC and with an anti-CD1a-PE antibody. Mounted slides were analysed by fluorescence microscopy and quantifications were performed on projected slides associated with a grid of 0.015 mm(2). Our results have shown that 1/ the number of CD1a+ LC was significantly increased (P = 0.01) when compared with Langerin+ LC 2/ 92% of Langerin+ LC co-expressed CD1a 3/ only 82% of CD1a+ cells coexpressed Langerin 4/ a positive correlation was noted between CD1a+ and Langerin+ LC numbers. The present study has revealed the heterogeneity in the phenotype of gingival LC population and shown that Langerin seems the most specific marker for the study of LC. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:255 / 262
页数:8
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