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Characterisation of interleukin-10 expression on different vascular structures in allergic nasal mucosa.

Authors :
Muller B
van Egmond D
de Groot EJ
Fokkens WJ
van Drunen CM
Source :
Clinical and translational allergy [Clin Transl Allergy] 2014 Jan 10; Vol. 4 (1), pp. 2. Date of Electronic Publication: 2014 Jan 10.
Publication Year :
2014

Abstract

Background: Interleukin-10 (IL-10) is a negative regulator of immune responses and was previously shown to be expressed by human nasal endothelial cells, while the adhesion molecule MECA-79 plays a role in trans-endothelial migration of immune competent cells. In this study we investigate the relationship between endothelial IL-10 and MECA-79 expression to address the question whether immune competent cells could be affected at the mucosal entry site.<br />Methods: Nasal turbinate biopsies were taken from house dust mite allergic patients, before and after nasal allergen provocation. Subsequent slides of biopsies were stained for IL10, MECA-79, CD34, and IL10-Receptor. Capillaries, arteries/veins, and sinusoids were evaluated separately.<br />Results: 90% of sinusoids are IL-10 positive and all sinusoids are negative for MECA-79, while 4.8% of capillaries are positive for IL-10, and 2.2% are positive for MECA-79. Although about 47% of arteries/veins are positive for IL-10 and 57.1% are positive for MECA-79, only about 20% are positive for both markers. Furthermore, we showed that the myo-fibroblasts surrounding all sinusoids stain positive for IL10R.<br />Conclusions: IL10 expression on vascular structures is not related to MECA expression for sinusoids and capillaries and only partly related on arteries/veins, however sinusoidal endothelial IL10 expression is always seen in combination with IL-10R expression of sinusoidal myo-fibroblasts.

Details

Language :
English
ISSN :
2045-7022
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
Clinical and translational allergy
Publication Type :
Academic Journal
Accession number :
24405811
Full Text :
https://doi.org/10.1186/2045-7022-4-2