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Effects of guluronic acid (G2013) on SHIP1, SOCS1 induction and related molecules in TLR4 signaling pathway.
Mortazavi-Jahromi, Seyed Shahabeddin; Farazmand, Ali; Motamed, Nasrin; Navabi, Shadi Sadat; Mirshafiey, Abbas.
  • Mortazavi-Jahromi SS; Department of Cellular and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran; Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  • Farazmand A; Department of Cellular and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran; School of Biology, University College of Science, University of Tehran, Tehran, Iran.
  • Motamed N; Department of Cellular and Molecular Biology, Kish International Campus, University of Tehran, Kish, Iran; School of Biology, University College of Science, University of Tehran, Tehran, Iran.
  • Navabi SS; Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
  • Mirshafiey A; Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: mirshafiey@tums.ac.ir.
Int Immunopharmacol ; 55: 323-329, 2018 Feb.
Article en En | MEDLINE | ID: mdl-29310108
ABSTRACT

OBJECTIVE:

This research aimed to study the anti-inflammatory and immunomodulatory effects of guluronic acid (G2013) on gene expression of TLR4, MyD88, SHIP1, SOCS1, NF-κB, and assessment of the level of IL-1ß as a pro-inflammatory cytokine in HEK-Blue hTLR4 cell line.

METHODS:

The cytotoxicity of G2013 was assessed by the MTT assay. The mRNA expression levels of the mentioned genes were measured by qRT-PCR. IL-1ß concentration in culture media was determined using ELISA method.

RESULTS:

MTT assay demonstrated that G2013 (before the concentration of 125µg/ml) had no cytotoxic effect on HEK-Blue hTLR4 cells. Our results indicated that the low and high doses of this drug could significantly reduce the gene expression of TLR4 and MyD88, as compared to the control group (p<0.05). Moreover, it was found that the low dose of this drug could significantly increase the gene expression of SHIP1 and SOCS1, as compared to the control group (p<0.05). Furthermore, the study findings revealed that the level of NF-κB gene expression significantly reduced, in both doses of G2013 compared to the control group (p<0.05, p<0.01, respectively). Our data showed that the level of IL-1ß in culture media decreased by both doses of this drug in comparison to control group (p<0.05).

CONCLUSION:

This study indicates that G2013 is able to induce SHIP1, SOCS1 and reduce TLR4, MyD88, NF-κB at the level of gene expression and decrease IL-1ß as a pro-inflammatory cytokine which might be recommended for reduction of inflammatory reactions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilinositol-3,4,5-Trifosfato 5-Fosfatasas / Proteína 1 Supresora de la Señalización de Citocinas / Ácidos Hexurónicos / Riñón / Antiinflamatorios Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilinositol-3,4,5-Trifosfato 5-Fosfatasas / Proteína 1 Supresora de la Señalización de Citocinas / Ácidos Hexurónicos / Riñón / Antiinflamatorios Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article