Anti-Inflammatory Effects of Metabolites from Antarctic Fungal Strain Pleosporales sp. SF-7343 in HaCaT Human Keratinocytes

Chemical investigation of the Antarctic fungi Pleosporales sp. SF-7343 revealed four known secondary fungal metabolites: alternate C ( 1 ), altenusin ( 2 ), alternariol ( 3 ), and altenuene ( 4 ). The compound structures were identified primarily by NMR and MS analyses. Atopic dermatitis, an inflamm...

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Bibliographic Details
Published in:International Journal of Molecular Sciences
Main Authors: Linsha Dong, Hye Jin Kim, Thao Quyen Cao, Zhiming Liu, Hwan Lee, Wonmin Ko, Youn-Chul Kim, Jae Hak Sohn, Tai Kyoung Kim, Joung Han Yim, Dong-Sung Lee, Hyuncheol Oh
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2021
Subjects:
Antarctic fungi
inflammation
ICAM-1
NF-κB
HO-1
HaCaT
Biology (General)
QH301-705.5
Chemistry
QD1-999
Antarctic
The Antarctic
Antarc*
Online Access:https://doi.org/10.3390/ijms22189674
https://doaj.org/article/8f66ce3af22f46d1842c98fef1041354
Description
Summary:Chemical investigation of the Antarctic fungi Pleosporales sp. SF-7343 revealed four known secondary fungal metabolites: alternate C ( 1 ), altenusin ( 2 ), alternariol ( 3 ), and altenuene ( 4 ). The compound structures were identified primarily by NMR and MS analyses. Atopic dermatitis, an inflammatory disease, is driven by the abnormal activation of T helper (Th) 2 cells and barrier dysfunction. We attempted to identify the anti-inflammatory components of SF-7343. Initial screening showed that compounds 1 and 3 inhibited the secretion of interleukin-8 and -6 in tumor necrosis factor-α/interferon-γ-treated HaCaT cells, and these compounds also showed inhibitory effects on CCL5 and CCL22. Compounds 1 and 3 also downregulated the protein expression levels of intercellular adhesion molecule-1 and upregulated the expression of filaggrin and involcurin. The mechanism study results showed that compounds 1 and 3 inhibited nuclear translocation of nuclear factor-kappa B p65 and the phosphorylation of STAT1 and STAT3. Compound 1 , but not compound 3 , significantly promoted the expression of heme oxygenase (HO)-1. The effects of compound 1 were partly reversed by co-treatment with a HO-1 inhibitor, tin protoporphyrin IX. Taken together, this study demonstrates the potential value of Antarctic fungal strain SF-7343 isolates as a bioresource for bioactive compounds to prevent skin inflammation.

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