β-Defensin 34, a crucial component of innate immunity, serves as a potent antimicrobial peptide that defends against a spectrum of pathogens. This peptide plays a pivotal role in the first line of defense by disrupting microbial membranes and exerting bactericidal effects, contributing to the overall host defense mechanism. Activation of β-defensin 34 involves a network of cellular signaling pathways influenced by various chemical activators. Compounds such as retinoic acid, thiazolidinediones, sulforaphane, butyrate, genistein, resveratrol, 5-azacytidine, alpha-lipoic acid, luteolin, diallyl disulfide, EGCG, and quercetin exert their effects through specific pathways, ranging from nuclear receptors to epigenetic modifications. These pathways converge at the DEFB34 promoter, leading to enhanced transcription and synthesis of β-defensin 34.
The multifaceted activation mechanisms highlight the adaptability and complexity of the innate immune system. These chemical activators reinforce host defenses, providing a robust antimicrobial response against a diverse array of microbial challenges. Understanding these activation pathways enhances our comprehension of the intricate interplay between the innate immune system and microbial invaders, opening avenues for future research in immunomodulation.
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