Celastrol binds to ERK and inhibits FcepsilonRI signaling to exert an anti-allergic effect.
The role of celastrol, a triterpene extracted from the Chinese "Thunder of God Vine," in allergic inflammation was investigated. Celastrol decreased the secretion of beta-hexosaminidase, decreased the release of histamine, decreased the expression of Th2 cytokines and decreased calcium influx and cell adhesion in antigen-stimulated RBL2H3 cells. Exposure to celastrol ... decreased the phosphorylation of extracellular regulated kinase (ERK) and the ERK kinase activity was decreased in RBL2H3 cells. A molecular dynamics simulation showed binding of celastrol to a large pocket in ERK2, which serves as the ATP-binding site. Exposure to celastrol inhibited the interaction between immunoglobulin Fc epsilon receptor I (FcepsilonRIgamma) and ERK and inhibited interaction between FcepsilonRIgamma and protein kinase C delta (PKCdelta). Antigen stimulation induced an interaction between Rac1 and ERK as well as an interaction between Rac1 and PKCdelta. Inhibition of ERK decreased Rac1 activity and inhibition of Rac1 decreased ERK activity in antigen-stimulated RBL2H3 cells. Celastrol regulated the expression of epithelial-mesenchymal transition (EMT)-related proteins through inhibition of PKCalpha, PKCdelta, and Rac1 in antigen-stimulated RBL2H3 cells. Exposure to celatrol inhibited PKCdelta activity in antigen-stimulated RBL2H3 cells. Celastrol exerted a negative effect on FcepsilonRIbeta signaling by inhibiting the interaction between heat shock protein 90 (hsp90) and proteins, such as, FcepsilonRIbeta, Akt and PKCalpha. Celastrol exerted a negative effect on in vivo atopic dermatitis induced by 2, 4-dinitrofluorobenzene (DNFB), which requires ERK. Celastrol also showed an inhibitory effect on skin inflammation induced by phorbol myristate acetate (PMA) in Balb/c mice. In summary, celastrol binds to ERK and inhibits FcepsilonRI signaling to exert an anti-inflammatory effect.
Mesh Terms:
Animals, Anti-Allergic Agents, Calcium, Cell Adhesion, Cell Line, Tumor, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Female, Histamine Release, Mice, Mice, Inbred BALB C, Mice, Inbred Strains, Rats, Receptors, IgE, Signal Transduction, Specific Pathogen-Free Organisms, Triterpenes, beta-N-Acetylhexosaminidases
Animals, Anti-Allergic Agents, Calcium, Cell Adhesion, Cell Line, Tumor, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Female, Histamine Release, Mice, Mice, Inbred BALB C, Mice, Inbred Strains, Rats, Receptors, IgE, Signal Transduction, Specific Pathogen-Free Organisms, Triterpenes, beta-N-Acetylhexosaminidases
Eur. J. Pharmacol.
Date: Jun. 10, 2009
PubMed ID: 19356729
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