Abstract

The innate and adaptive immune systems play an essential role in host defense against pathogens. Various signal transduction pathways monitor and balance the immune system since an imbalance may promote pathological states such as allergy, inflammation, and cancer. Mast cells have a central role in the regulation of the innate/adaptive immune system and are involved in the pathogenesis of many inflammatory and allergic diseases by releasing inflammatory mediators such as histamines, proteases, chemotactic factors, and cytokines. Although various signaling pathways are associated with mast cell activation, our discovery and characterization of the pLysRS-Ap4A signaling pathway in these cells provided an additional important step towards a full understanding of the intracellular mechanisms involved in mast cell activation. In the present review, we will discuss in depth this signaling pathway’s contribution to host defense and the pathological state.

Highlights

  • Maturation of mast cells (MCs) occurs in these vascular tissues aided by cytokines, stem cell factors secreted by fibroblasts and endothelial cells [1]

  • We identified by Biacore analysis that specific binding of histidine triad nucleotide-binding protein 1 (HINT1) to Ap4 A, but not to other Apn A molecules (Ap3 A or Ap5 A), affected the MITF–HINT-1 protein

  • The discovery and characterization of the p-lysyl-tRNA synthetase (LysRS)-Ap4A signaling pathway has attracted the attention of many researchers

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Summary

Role oflocation pLysRS-Ap under Pathological

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Autoimmune Disease
Tumor Microenvironment
Asignaling
Conclusions
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