Cooperation of adapter molecules in proximal signaling cascades during allergic inflammation

• Published in: Immunological reviews Vol. 232; no. 1; pp. 99 - 114
• Main Authors: Kambayashi, Taku, LaRosa, David F, Silverman, Michael A, Koretzky, Gary A
• Format: Journal Article
• Language: English
• Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01-11-2009; Blackwell Publishing Ltd
• Subjects: adapter molecules; Adaptor Proteins, Signal Transducing - immunology; allergy; Animals; cell signaling; FcεRI; Humans; hypersensitivity; Hypersensitivity - immunology; Hypersensitivity - metabolism; mast cell; Mast Cells - cytology; Mast Cells - immunology; Mast Cells - metabolism; Protein Multimerization - immunology; Receptor Cross-Talk; Receptors, IgE - immunology; Receptors, IgE - metabolism; Signal Transduction - immunology; TLR; Toll-Like Receptors - metabolism
• ISSN: 0105-2896; 1600-065X
• DOI: 10.1111/j.1600-065X.2009.00825.x

Activation of mast cells through their high-affinity immunoglobulin E receptor (FcεRI) plays an important role in allergic disorders. Other mast cell-activating stimuli, such as Toll-like receptor (TLR) ligands, synergize with FcεRI to enhance allergic inflammation. Thus, there is much interest in understanding how signaling occurs downstream of these receptors. One key event for FcεRI-mediated mast cell activation is the inducible formation of multimolecular proximal signaling complexes. These complexes are nucleated by adapter proteins, scaffolds that localize various signaling molecules through their multiple molecule-binding domains. Here we review recent findings in proximal signaling cascades with an emphasis on how adapter molecules cooperate with each other to generate an optimal signal in mast cells, and we discuss how signals crosstalk between FcεRI and TLRs in enhancing mast cell activation. Deciphering the molecular mechanisms leading to mast cell activation will hopefully bring new ideas for the development of novel therapeutics to control allergic diseases.