β-Defensin 28, a crucial component of the innate immune system, plays a pivotal role in defending against microbial threats. As an antimicrobial peptide, it contributes to the first line of defense by disrupting microbial membranes and exerting bactericidal effects. Understanding the mechanisms governing β-defensin 28 activation provides insights into the intricate interplay between cellular pathways and immune responses.
Activation of β-defensin 28 involves a network of cellular signaling cascades 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 directly or indirectly enhance β-defensin 28 expression. These activators act through diverse pathways, including retinoic acid receptors, PPARγ, Keap1-Nrf2-ARE, histone deacetylation, PI3K/Akt, Nrf2/ARE, AP-1, MAPK, and NF-κB. By modulating chromatin structure, transcription factor activity, and epigenetic modifications, these chemicals contribute to the up-regulation of β-defensin 28, reinforcing the innate immune response against microbial invaders. The comprehensive understanding of these activation mechanisms provides a foundation for exploring potential strategies to enhance innate immunity and combat microbial infections.
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