Shih JH et al. (2020), Hp-s1 Ganglioside Suppresses Proinflammatory Re...

ECB-ART-49578

Mar Drugs 2020 Sep 29;1810:. doi: 10.3390/md18100496.

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Hp-s1 Ganglioside Suppresses Proinflammatory Responses by Inhibiting MyD88-Dependent NF-κB and JNK/p38 MAPK Pathways in Lipopolysaccharide-Stimulated Microglial Cells.

Shih JH , Tsai YF , Li IH , Chen MH , Huang YS .

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Hp-s1 ganglioside is isolated from the sperm of sea urchin (Hemicentrotus pulcherrimus). In addition to neuritogenic activity, the biological function of Hp-s1 in neuroinflammation is unknown. In this study, we investigated the anti-neuroinflammatory effect of Hp-s1 on lipopolysaccharide (LPS)-stimulated microglial cells. MG6 microglial cells were stimulated with LPS in the presence or absence of different Hp-s1 concentrations. The anti-inflammatory effect and underlying mechanism of Hp-s1 in LPS-activated microglia cells were assessed through a Cell Counting kit-8 assay, Western blot analysis, and immunofluorescence. We found that Hp-s1 suppressed not only the expression of inducible nitric oxide synthase and cyclooxygenase-2 but also the expression of proinflammatory cytokines, such as TNF-α, IL-1β, and IL-6. Hp-s1 inhibited the LPS-induced NF-κB signaling pathway by attenuating the phosphorylation and translocation of NF-κB p65 and by disrupting the degradation and phosphorylation of inhibitor κB-α (IκBα). Moreover, Hp-s1 inhibited the LPS-induced phosphorylation of p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK). Hp-s1 also reduced the expression of myeloid differentiation factor 88 (MyD88) and TNF receptor-associated factors 6 (TRAF6), which are prerequisites for NF-κB and MAPKs activation. These findings indicated that Hp-s1 alleviated LPS-induced proinflammatory responses in microglial cells by downregulating MyD88-mediated NF-κB and JNK/p38 MAPK signaling pathways, suggesting further evaluation as a new anti-neuroinflammatory drug.

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	Figure 1. Effect of Hp-s1 ganglioside on cell viability of MG6 microglial cells. The cells were cultured with different Hp-s1 concentrations (5â100 Î¼M) for 24 h. The cell viability was determined via a CCK-8 assay. Quantitative data were expressed as the percentage of the corresponding untreated control value (mean Â± S.D., n = 3, quadruplicate wells for each condition).
	Figure 2. Hp-s1 suppresses the lipopolysaccharide (LPS)-induced expression of iNOS and COX-2 in a dose-dependent manner. (A) The cells were pretreated with Hp-s1 (5, 15, or 30 Î¼M) for 2 h and then treated with or without LPS (1âÎ¼g/mL) for another 8 h. Total lysates were collected, and the protein levels of iNOS and COX-2 were detected via Western blot analysis. Î²-actin was used as an internal control. (B) The protein bands of each regimen were quantified through densitometry. Data were expressed as the percentage of the LPS-treated group (mean Â± S.D., n = 3). ## p < 0.01 vs. the control group; ** p < 0.01 vs. the LPS-treated group. (C) Immunofluorescence staining for iNOS and COX-2. Cells were pretreated with 30 Î¼M Hp-s1 for 2 h and then stimulated with or without LPS (1 Î¼g/mL) for 8 h. The cells were immunostained with anti-iNOS and anti-COX-2 antibodies. The nuclei (blue) were stained with 4â²,6-diamidino-2-phenylindole (DAPI). Bar = 30 Î¼m.
	Figure 3. Hp-s1 suppresses proinflammatory cytokines in LPS-stimulated microglial cells. (A) The cells were pretreated with different Hp-s1 concentrations (5, 15, or 30 Î¼M) in the absence or presence of LPS (1 Î¼g/mL) for 8 h and then subjected to Western blot analysis with anti-TNF-Î±, anti-IL-1Î², and IL-6 antibodies; Î²-actin was used as an internal control. (B) The protein bands of each regimen were quantified via densitometry. Data were expressed as the percentage of the LPS-treated group (mean Â± S.D., n = 3). ## p < 0.01 vs. the control group; * p < 0.05 and ** p < 0.01 vs. the LPS-treated group. (C) Immunofluorescence staining for TNF-Î±. and IL-6. The cells were pretreated with 30 Î¼M Hp-s1 for 2 h and then stimulated with or without LPS (1 Î¼g/mL) for 8 h. The cells were immunostained with anti-TNF-Î± and IL-6 antibodies. The nuclei (blue) were stained with DAPI. Bar = 30 Î¼m.
	Figure 4. Hp-s1 inhibits the LPS-induced NF-ÎºB activation. (A) The cells were pretreated with different Hp-s1 concentrations (5, 15, or 30 Î¼M) for 2âh and then stimulated with LPS (1 Î¼g/mL) for 1âh. Cell lysates were subjected to Western blot to determine the protein levels of p-p65, p65, p-IÎºBÎ±, and IÎºBÎ±. Î²-actin was used as an internal control. (B) The protein bands of each regimen were quantified via densitometry. Data were expressed as the percentage of the LPS-treated group (mean Â± S.D., n = 3). ## p < 0.01 vs. the control group; * p < 0.05 and ** p < 0.01 vs. the LPS-treated group. (C) Immunofluorescence analysis of NF-ÎºB translocation. The cells were pretreated with Hp-s1 (30 Î¼M) for 2 h and then activated with LPS (1 Î¼g/mL) for 1 h. The translocation of the p65 subunit of NF-ÎºB was determined via immunocytochemistry using anti-p65 NF-ÎºB antibody. The nuclei (blue) were stained with DAPI. Scale bar = 30 Î¼m.
	Figure 5. Hp-s1 inhibits the LPS-induced JNK/p38 MAPK activation. (A) The cells were pretreated with different Hp-s1 concentrations (5, 15, or 30 Î¼M) for 2âh and then stimulated with or without LPS (1 Î¼g/mL) for 1 h. Cell lysates were subjected to Western blot to determine the protein levels of MAPKs (p-p38/p38, p-JNK/JNK, and p-ERK/ERK). Î²-actin was used as an internal control. (BâD) The protein bands of each regimen were quantified via densitometry. Data were expressed as the percentage of the LPS-treated group (mean Â± S.D., n = 3). ## p < 0.01 and á´ª p < 0.05 vs. the control group; * p < 0.05 and ** p < 0.01 vs. the LPS-treated group.
	Figure 6. Hp-s1 blocks the LPS-induced MyD88/TRAF6-dependent signaling pathway in MG6 microglial cells. (A) The cells were pretreated with different Hp-s1 concentrations (5, 15, or 30 Î¼M) for 2 h and then stimulated with or without LPS (1 Î¼g/mL) for 40 min. Cell lysates were subjected to Western blot to determine the protein levels of TLR4, MyD88, and TRAF6. Î²-actin was used as an internal control. (BâD) The protein bands of each regimen were quantified via densitometry. Data were expressed as the percentage of the LPS-treated group (mean Â± S.D., n = 3). ## p < 0.01 vs. the control group; * p < 0.05 vs. the LPS-treated group.
	Figure 7. Schematic of the anti-inflammatory action of Hp-s1. Hp-s1 inhibited the proinflammatory reactions in MG6 microglial cells by repressing the MyD88/TRAF6-dependent NF-ÎºB and JNK/p38 MAPK signaling pathways.

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Azam, Regulation of Toll-Like Receptor (TLR) Signaling Pathway by Polyphenols in the Treatment of Age-Linked Neurodegenerative Diseases: Focus on TLR4 Signaling. 2019, Pubmed