| Literature DB >> 28343320 |
David Schmit1, Duc Dung Le1, Sebastian Heck1, Markus Bischoff2, Thomas Tschernig3, Christian Herr4, Christoph Beisswenger4, Peter Kobelt5, Phillipp Moritz Lepper4, Kian Fan Chung6, Robert Bals4, Quoc Thai Dinh7,8.
Abstract
Mast cells (MCs) and airway nerves play an important role in allergic asthma. However, little is known about the MCs and their interaction with airway nerves during allergic airway inflammation. This study aims to investigate the distribution and proliferation of MC populations in different lung compartments, along with the association of mast cells with nerve endings, using a house dust mite (HDM) model for allergic airway inflammation. BALB/c mice were exposed to HDM extract intranasally (25 μg/50 μl) for 5 consecutive days a week over 7 weeks. Immunofluorescence and Edu stains were used to examine the colocalisation of MCs and nerves and the proliferation of MCs, respectively. HDM treatment caused an increased migration of MCs into bronchi, alveolar parenchyma and airway vessels. The proportions of tryptase-chymase expressing MC (MCTC) increased significantly in the bronchi and the alveolar parenchyma but not in the vascular tissues, by allergic airway inflammation. The association of MCs with nerves was found only in the bronchi and there were no changes in comparison of controls to HDM-treated animals. The present study shows a strong migration of tryptase expressing MC (MCT) and MCTC into the bronchi and the alveolar parenchyma, as well as of MCT in the vascular compartment under HDM treatment. This supports the hypothesis that these mast cell populations may contribute to allergic airway inflammation.Entities:
Keywords: Allergic airway inflammation; Chymase; Mast cells; Neuroimmune Interaction; Tryptase
Mesh:
Year: 2017 PMID: 28343320 DOI: 10.1007/s00441-017-2597-9
Source DB: PubMed Journal: Cell Tissue Res ISSN: 0302-766X Impact factor: 5.249