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Water-based extracts of Zizania latifolia inhibit Staphylococcus aureus infection through the induction of human beta-defensin 2 expression in HaCaT cells.

Abstract
Zizania latifolia is a perennial herb belonging to the family Gramineae that has been used as a health food in Asian countries. In this study, we investigated the antimicrobial effect of Z. latifolia, which increased human beta-defensin 2 (hBD2) expression in HaCaT cells. hBD2 expression was further increased in cells treated with Z. latifolia extracts and subsequently infected with Staphylococcus aureus. Inversely, S. aureus infection decreased after treatment. The induction of hBD2 in HaCaT cells was mediated by the Toll-like receptor 2 (TLR2) signaling pathway, including the activation of extracellular signal-regulated kinase (ERK) and activator protein 1 (AP-1). Further study using siRNA revealed that hBD2 played an important role in the inhibition of S. aureus infection in HaCaT cells. Our data suggest that Z. latifolia extracts can be used as an antimicrobial ingredient for skin treatment formulas.
AuthorsBo Yeon Kang, Seung-Su Lee, Myun-Ho Bang, Hyoik Jeon, Hangeun Kim, Dae Kyun Chung
JournalJournal of microbiology (Seoul, Korea) (J Microbiol) Vol. 56 Issue 12 Pg. 910-916 (Dec 2018) ISSN: 1976-3794 [Electronic] Korea (South)
PMID30484159 (Publication Type: Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • DEFB4A protein, human
  • Plant Extracts
  • RNA, Small Interfering
  • TLR2 protein, human
  • Toll-Like Receptor 2
  • Transcription Factor AP-1
  • beta-Defensins
  • Water
  • Extracellular Signal-Regulated MAP Kinases
Topics
  • Anti-Bacterial Agents (pharmacology)
  • Cell Line (drug effects)
  • Extracellular Signal-Regulated MAP Kinases (metabolism)
  • Gene Expression Regulation (drug effects)
  • Humans
  • Immunity, Innate (drug effects)
  • Plant Extracts (pharmacology)
  • Poaceae (chemistry)
  • RNA, Small Interfering
  • Signal Transduction
  • Staphylococcal Skin Infections (therapy)
  • Staphylococcus aureus (drug effects)
  • Toll-Like Receptor 2 (metabolism)
  • Transcription Factor AP-1 (metabolism)
  • Water
  • beta-Defensins (drug effects, metabolism)

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