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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and <t>p-IκBα</t> was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.
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Image Search Results


LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and p-IκBα was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.

Journal: International Dental Journal

Article Title: NLRP12 Alleviated Periodontal Destruction via Suppressing Nuclear Factor Kappa-B Signalling Pathway

doi: 10.1016/j.identj.2026.109417

Figure Lengend Snippet: LPS inhibited the expression of NLRP12 and promoted the activation of the NF-κB signalling pathway in PDLSCs. (A) The expression level of NLRP12 in PDLSCs after LPS treatment was detected by immunofluorescence staining (scale bar = 50 μm). The qRT-PCR (B) and WB (C) analysis revealed significantly reduced expression of NLRP12 in PDLSCs after treatment with 10 µg/mL LPS. (D) WB analysis demonstrated that the expression of p-p65 and p-IκBα was significantly elevated relative to GAPDH in PDLSCs treated with 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). *** P < .001, **** P < .0001.

Article Snippet: After blocking with rapid sealing fluid for 30 minutes, the membranes were incubated with primary antibodies, including COL1 (#12256; CST), RUNX2 (#8486; CST), NLRP12 (#DF14960; Affinity Biosciences), phospho-p65 (p-p65) (#3033; CST), p65 (#8242; CST), p-IκBα (#2859; CST), IκBα (#4814; CST), GAPDH (#60004; Proteintech) overnight at 4°C.

Techniques: Expressing, Activation Assay, Immunofluorescence, Staining, Quantitative RT-PCR

Overexpression of NLRP12 alleviated the inflammatory responses and osteogenic differentiation inhibition of PDLSCs by suppressing the NF-κB pathway. (A) WB results showing the changes of protein expression levels of p-p65, p65, p-IκBα, and IκBα in PDLSCs after NLRP12 overexpression. (B) WB results showing the changes of protein expression levels of p-p65 and p65 in PDLSCs overexpressing NLRP12 after PMA treatment. (C)The qRT-PCR results demonstrating the transcriptional expression levels of IL-6, IL-8 , and IL-10 in PDLSCs overexpressing NLRP12 after PMA treatment. (D)WB results demonstrating alterations in the protein expression levels of COL1 and RUNX2 in PDLSCs overexpressing NLRP12 after PMA treatment. (E) Representative pictures showing ALP staining (scale bar = 500 μm) (F) Representative pictures showing alizarin red staining (scale bar = 500 μm). oeNC: PDLSCs transfected via negative control lentiviral. oeNLRP12: PDLSCs transfected via lentiviral with overexpression- NLRP12 . oeNC + LPS: PDLSCs transfected via negative control lentiviral and subsequently cultured under 10 µg/mL LPS. oeNLRP12 + LPS: PDLSCs transfected via lentiviral with overexpression- NLRP12 and subsequently cultured under 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). ns, no significant difference, * P < .05, ** P < .01, *** P < .001, **** P < .0001.

Journal: International Dental Journal

Article Title: NLRP12 Alleviated Periodontal Destruction via Suppressing Nuclear Factor Kappa-B Signalling Pathway

doi: 10.1016/j.identj.2026.109417

Figure Lengend Snippet: Overexpression of NLRP12 alleviated the inflammatory responses and osteogenic differentiation inhibition of PDLSCs by suppressing the NF-κB pathway. (A) WB results showing the changes of protein expression levels of p-p65, p65, p-IκBα, and IκBα in PDLSCs after NLRP12 overexpression. (B) WB results showing the changes of protein expression levels of p-p65 and p65 in PDLSCs overexpressing NLRP12 after PMA treatment. (C)The qRT-PCR results demonstrating the transcriptional expression levels of IL-6, IL-8 , and IL-10 in PDLSCs overexpressing NLRP12 after PMA treatment. (D)WB results demonstrating alterations in the protein expression levels of COL1 and RUNX2 in PDLSCs overexpressing NLRP12 after PMA treatment. (E) Representative pictures showing ALP staining (scale bar = 500 μm) (F) Representative pictures showing alizarin red staining (scale bar = 500 μm). oeNC: PDLSCs transfected via negative control lentiviral. oeNLRP12: PDLSCs transfected via lentiviral with overexpression- NLRP12 . oeNC + LPS: PDLSCs transfected via negative control lentiviral and subsequently cultured under 10 µg/mL LPS. oeNLRP12 + LPS: PDLSCs transfected via lentiviral with overexpression- NLRP12 and subsequently cultured under 10 µg/mL LPS. Data were presented as mean ± SD ( n = 3). ns, no significant difference, * P < .05, ** P < .01, *** P < .001, **** P < .0001.

Article Snippet: After blocking with rapid sealing fluid for 30 minutes, the membranes were incubated with primary antibodies, including COL1 (#12256; CST), RUNX2 (#8486; CST), NLRP12 (#DF14960; Affinity Biosciences), phospho-p65 (p-p65) (#3033; CST), p65 (#8242; CST), p-IκBα (#2859; CST), IκBα (#4814; CST), GAPDH (#60004; Proteintech) overnight at 4°C.

Techniques: Over Expression, Inhibition, Expressing, Quantitative RT-PCR, Staining, Transfection, Negative Control, Cell Culture