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In vitro , quercetin pre-treatment (10 M) inhibited Rhinovirus (RV) virulence, entry, and replication into BEAS-2B cells via multiple mechanisms: it impeded RV endocytosis though misdirecting EEA1 localization -an early endosomal marker- and inhibiting AKT phosphorylation with subsequent 3-fold viral load reduction at 24 h, lowering negative-strand RNA and modulating interferon (IFN) and IL-8 expression (70)

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During metestrus, SNE and LNE numbers increase, AKE numbers decrease, and LEU numbers increase but cluster around SNE and LNEs

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