Abstract

Orai1 is the key subunit of the Ca2+-release-activated Ca2+ channel. Our previous report has demonstrated that Orai1 expression in the airway was upregulated in the ovalbumin (OVA)-induced allergic rhinitis (AR) mouse models. To observe whether inhibition of Orai1 expression in the airway could suppress symptoms in a murine model of AR and to assess the impacts of this inhibition on the responses of local and systemic immunocytes, we administered recombinant lentivirus vectors that encoded shRNA against ORAI1 (lenti-ORAI1) into the nostrils of OVA-sensitized mice before the challenges, and analyzed its effect on allergic responses, as compared with the unsensitized mice and untreated AR mice. Administration of lenti-ORAI1 into the nasal cavity successfully infected cells in the epithelial layer of the nasal mucosa, and significantly decreased the frequencies of sneezing and nasal rubbing of the mice. Protein levels of leukotriene C4, OVA-specific IgE, and IL-4 in the nasal lavage fluid and serum and eosinophil cation protein in the serum were also significantly reduced by lenti-ORAI1, as were the mRNA levels of these factors in the nasal mucosa and spleen. These data suggested that administration of lenti-ORAI1 into the nasal cavity effectively decreased Orai1 expression in the nasal mucosa, alleviated AR symptoms, and partially inhibited the hyperresponsiveness of the local and systemic immune cells including T cells, B cells, mast cells and eosinophils that are involved in the pathogenesis of AR.

Highlights

  • Allergic rhinitis (AR) is allergic inflammation in the upper airway associated with the hyperresponsiveness of several types of immune cells

  • 2-aminoethoxydiphenyl borate (2-APB) has been known to interfere with a variety of transport processes besides Ca2+-release-activated Ca2+ (CRAC) channels, including K+ channels (Wang et al, 2002) and mitochondrial Ca2+ efflux (Prakriya and Lewis, 2001)

  • Ca2+ signals are vital in the function of many cell types of the immune system, including T cells, B cells, NK cells, mast cells, dendritic cells, and macrophages, and they control cell functions as diverse as differentiation, proliferation, gene expression, cell motility, and the secretion of vesicles that contain cytokines, cytotoxic proteins, and/or proinflammatory proteins (Feske, 2007; Gwack et al, 2007)

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Summary

Introduction

Allergic rhinitis (AR) is allergic inflammation in the upper airway associated with the hyperresponsiveness of several types of immune cells. With the help of antigen presenting cells (APCs), an allergen triggers a Th2-predominant immune response that leads to the generation of memory B cells that produce antigen-specific IgE. This IgE binds to mast cells, and subsequent exposure to the allergen provokes these IgE-binding mast cells to release inflammatory mediators, such as histamine and leukotriene C4 (LTC4), that induce allergic reactions. Mainstream therapy for AR consists of disease control through the use of anti-inflammatory agents, glucocorticoidbased drugs, antihistamines, and antileukotrienes. These drugs relieve symptoms in most patients, they do not cure the underlying disease. The challenge to develop safe, new therapeutic agents that target the root of the pathogenesis of AR remains

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