Date published: 2025-10-12

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Ear14 Activators

Ear14, a member of the eosinophil-associated ribonuclease A family, plays a pivotal role in orchestrating innate immune responses with a multifaceted functionality. Predicted to enable ribonuclease activity, Ear14 is anticipated to participate in crucial cellular processes, particularly in chemotaxis and innate immune responses within mucosal tissues. Its extracellular localization underscores its involvement in modulating responses at the interface between the host organism and potential environmental challenges. Orthologous to the human RNASE2, Ear14 shares evolutionary significance with a related ribonuclease family member, further emphasizing its essential role in maintaining cellular homeostasis and defense mechanisms. The activation of Ear14 involves a sophisticated interplay of various cellular mechanisms and signaling pathways, contributing to its dynamic engagement in innate immunity. These mechanisms include histone acetylation, cAMP-mediated signaling, and the modulation of key signaling pathways such as NF-κB and Wnt. Histone acetylation, influenced by chemicals like sodium butyrate and trichostatin A, creates a permissive chromatin environment that facilitates gene expression, indirectly promoting Ear14 activation. Forskolin, by activating adenylate cyclase and increasing cAMP levels, stimulates protein kinase A, influencing chemotaxis and innate immune responses and indirectly contributing to Ear14 expression.

Moreover, modulation of NF-κB signaling by chemicals like quercetin and curcumin plays a crucial role in regulating genes associated with innate immunity, indirectly influencing Ear14. Sodium salicylate, through the inhibition of NF-κB, contributes to the suppression of pathways related to mucosal immune responses, indirectly impacting Ear14 activation. Lithium chloride, by activating the Wnt signaling pathway, indirectly influences Ear14 expression, providing another layer of regulatory control over its involvement in innate immunity. Additionally, the redox-sensitive pathways influenced by N-acetyl cysteine and the Nrf2-activating property of sulforaphane contribute to Ear14 activation by impacting cellular redox balance. Collectively, the intricate network of these diverse cellular processes and signaling events highlights the sophisticated regulatory landscape through which Ear14 fulfills its crucial role in orchestrating innate immune responses, particularly within mucosal tissues.

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