miRNA-203b-3p Induces Acute and Chronic Pruritus through 5-HTR2B and TRPV4

TRPV4
DOI: 10.1016/j.jid.2022.08.034 Publication Date: 2022-08-30T01:01:29Z
ABSTRACT
Growing evidence indicates that transient receptor potential (TRP) channels contribute to different forms of pruritus. However, the endogenous mediators cause itch through signaling are poorly understood. In this study, we show genetic deletion or pharmacological antagonism TRPV4 attenuated in a mouse model psoriasis induced by topical application imiquimod. Human psoriatic lesions showed increased expression several microRNAs, including miR-203b-3p, which calcium ion response rodent dorsal root ganglion neurons and scratching behavior mice 5-HTR2B activation protein kinase C‒dependent phosphorylation TRPV4. Computer simulation revealed miR-203b-3p core sequence (GUUAAGAA) causes 5-HTR2B/TRPV4-dependent targets extracellular side interacting with portion pocket consistent its activation. Overall, reveal unconventional pathophysiological role an microRNA can behave as promoter
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