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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.
- Source :
-
Journal of microbiology (Seoul, Korea) [J Microbiol] 2018 Dec; Vol. 56 (12), pp. 910-916. Date of Electronic Publication: 2018 Nov 27. - Publication Year :
- 2018
-
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.
- Subjects :
- Cell Line drug effects
Extracellular Signal-Regulated MAP Kinases metabolism
Gene Expression Regulation drug effects
Humans
Immunity, Innate drug effects
RNA, Small Interfering
Signal Transduction
Toll-Like Receptor 2 metabolism
Transcription Factor AP-1 metabolism
Water
beta-Defensins drug effects
Anti-Bacterial Agents pharmacology
Plant Extracts pharmacology
Poaceae chemistry
Staphylococcal Skin Infections therapy
Staphylococcus aureus drug effects
beta-Defensins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1976-3794
- Volume :
- 56
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of microbiology (Seoul, Korea)
- Publication Type :
- Academic Journal
- Accession number :
- 30484159
- Full Text :
- https://doi.org/10.1007/s12275-018-8307-9