4.7 Article

Urolithin A Inactivation of TLR3/TRIF Signaling to Block the NF-κB/STAT1 Axis Reduces Inflammation and Enhances Antioxidant Defense in Poly(I:C)-Induced RAW264.7 Cells

期刊

出版社

MDPI
DOI: 10.3390/ijms23094697

关键词

urolithin A; poly(I:C); TLR3; NF-kappa B; MAPK

资金

  1. Chang Gung Memorial Hospital [CMRPF1K0082, CMRPF1L0011, CMRPF1J0042]
  2. Ministry of Science and Technology [109-2320-B-255-006-MY3]
  3. Chang Gung University of Science and Technology [ZRRPF3K0111 ZRRPF3L0091]

向作者/读者索取更多资源

Urolithin A, an active compound found in gut microbiota-derived metabolites of polyphenol ellagic acid, has been shown to have anti-aging, antioxidative, and anti-inflammatory effects. This study investigated the effects of urolithin A on poly(I:C)-induced inflammation in immune cells. The results demonstrated that urolithin A attenuated the inflammatory response and regulated various signaling pathways involved in inflammation and antioxidation. These findings suggest that urolithin A may have antiviral effects and could potentially be used as a treatment for viral-infection-related diseases.
Urolithin A is an active compound of gut-microbiota-derived metabolites of polyphenol ellagic acid that has anti-aging, antioxidative, and anti-inflammatory effects. However, the effects of urolithin A on polyinosinic acid-polycytidylic acid (poly(I:C))-induced inflammation remain unclear. Poly(I:C) is a double-stranded RNA (dsRNA) similar to a virus and is recognized by Toll-like receptor-3 (TLR3), inducing an inflammatory response in immune cells, such as macrophages. Inflammation is a natural defense process of the innate immune system. Therefore, we used poly(I:C)-induced RAW264.7 cells and attenuated the inflammation induced by urolithin A. First, our data suggested that 1-30 mu M urolithin A does not reduce RAW264.7 cell viability, whereas 1 mu M urolithin A is sufficient for antioxidation and the decreased production of tumor necrosis factor-alpha (TNF-alpha), monocyte chemoattractant protein-1 (MCP-1), and C-C chemokine ligand 5. The inflammation-related proteins cyclooxygenase-2 and inducible nitric oxide synthase were also downregulated by urolithin A. Next, 1 mu M urolithin A inhibited the levels of interferon (INF)-alpha and INF-beta. Urolithin A was applied to investigate the blockade of the TLR3 signaling pathway in poly(I:C)-induced RAW264.7 cells. Moreover, the TLR3 signaling pathway, subsequent inflammatory-related pathways, and antioxidation pathways showed changes in nuclear factor-kappa B (NF-kappa B) signaling and blocked ERK/mitogen-activated protein kinase (MAPK) signaling. Urolithin A enhanced catalase (CAT) and superoxide dismutase (SOD) activities, but decreased malondialdehyde (MDA) levels in poly(I:C)-induced RAW264.7 cells. Thus, our results suggest that urolithin A inhibits TLR3-activated inflammatory and oxidative-associated pathways in macrophages, and that this inhibition is induced by poly(I:C). Therefore, urolithin A may have antiviral effects and could be used to treat viral-infection-related diseases.

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