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Procell Inc rat kidney epithelial cell line nrk 52e
Rat Kidney Epithelial Cell Line Nrk 52e, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rat+kidney+epithelial+cell+line+nrk+52e/bronchial+cells+epithelial+human/10__1615_slash_critrevimmunol__2026061077-21-0-7
Average 86 stars, based on 1 article reviews
rat kidney epithelial cell line nrk 52e - by Bioz Stars, 2026-09
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Article Title: Combined Ursolic Acid and Rosuvastatin Treatment Mitigates Inflammation and Oxidative Stress in Diabetic Nephropathy Model Cells
Article Snippet: Background: Ursolic acid (UA) and Rosuvastatin (RST) improves diabetic nephropathy (DN).. However, the combination therapy of UA and RST on DN and its possible mechanism requires exploration.. Methods: Streptozotocin (STZ)-induced DN model cells were treated with UA and RST alone or in combination.



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Figure 2. IS induced ER stress, ferroptosis, and <t>epithelial–mesenchymal</t> transition (EMT) through ROS signaling in the renal tubular cells. <t>NRK-52E</t> cells were treated with various concentrations of IS (0.1–1 mM) for 24 h with or without pretreatment of 1 mM NAC for 1 h or 50 µM deferoxamine (DFO) for 1 h. (A,B) Western blot analysis and quantification for ER stress-related GRP78, p-eIF2α, ATF4, ATF6, and CHOP (A), and ferroptosis-related GPX4, PTGS2, and xCT (B) protein expression. (C) Western blot analysis and quantification for ATF4, CHOP, GPX4, and PTGS2 protein expression in IS-treated NRK-52E cells with or without NAC. (D) Western blot analysis and quantification for EMT-related fibronectin, E-cadherin, and vimentin protein expression in the IS-treated NRK-52E cells with or without NAC or DFO. Data are presented as means ± SD (n = 6 in (A–D); independent experiments). *, p < 0.05, compared with the control (C) group. #, p < 0.05, compared with the corresponding concentrations of IS groups. One-way ANOVA followed by Tukey’s post hoc test was used to analyze statistical differences.
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Figure 2. IS induced ER stress, ferroptosis, and <t>epithelial–mesenchymal</t> transition (EMT) through ROS signaling in the renal tubular cells. <t>NRK-52E</t> cells were treated with various concentrations of IS (0.1–1 mM) for 24 h with or without pretreatment of 1 mM NAC for 1 h or 50 µM deferoxamine (DFO) for 1 h. (A,B) Western blot analysis and quantification for ER stress-related GRP78, p-eIF2α, ATF4, ATF6, and CHOP (A), and ferroptosis-related GPX4, PTGS2, and xCT (B) protein expression. (C) Western blot analysis and quantification for ATF4, CHOP, GPX4, and PTGS2 protein expression in IS-treated NRK-52E cells with or without NAC. (D) Western blot analysis and quantification for EMT-related fibronectin, E-cadherin, and vimentin protein expression in the IS-treated NRK-52E cells with or without NAC or DFO. Data are presented as means ± SD (n = 6 in (A–D); independent experiments). *, p < 0.05, compared with the control (C) group. #, p < 0.05, compared with the corresponding concentrations of IS groups. One-way ANOVA followed by Tukey’s post hoc test was used to analyze statistical differences.
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Figure 2. IS induced ER stress, ferroptosis, and <t>epithelial–mesenchymal</t> transition (EMT) through ROS signaling in the renal tubular cells. <t>NRK-52E</t> cells were treated with various concentrations of IS (0.1–1 mM) for 24 h with or without pretreatment of 1 mM NAC for 1 h or 50 µM deferoxamine (DFO) for 1 h. (A,B) Western blot analysis and quantification for ER stress-related GRP78, p-eIF2α, ATF4, ATF6, and CHOP (A), and ferroptosis-related GPX4, PTGS2, and xCT (B) protein expression. (C) Western blot analysis and quantification for ATF4, CHOP, GPX4, and PTGS2 protein expression in IS-treated NRK-52E cells with or without NAC. (D) Western blot analysis and quantification for EMT-related fibronectin, E-cadherin, and vimentin protein expression in the IS-treated NRK-52E cells with or without NAC or DFO. Data are presented as means ± SD (n = 6 in (A–D); independent experiments). *, p < 0.05, compared with the control (C) group. #, p < 0.05, compared with the corresponding concentrations of IS groups. One-way ANOVA followed by Tukey’s post hoc test was used to analyze statistical differences.
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Figure 2. IS induced ER stress, ferroptosis, and epithelial–mesenchymal transition (EMT) through ROS signaling in the renal tubular cells. NRK-52E cells were treated with various concentrations of IS (0.1–1 mM) for 24 h with or without pretreatment of 1 mM NAC for 1 h or 50 µM deferoxamine (DFO) for 1 h. (A,B) Western blot analysis and quantification for ER stress-related GRP78, p-eIF2α, ATF4, ATF6, and CHOP (A), and ferroptosis-related GPX4, PTGS2, and xCT (B) protein expression. (C) Western blot analysis and quantification for ATF4, CHOP, GPX4, and PTGS2 protein expression in IS-treated NRK-52E cells with or without NAC. (D) Western blot analysis and quantification for EMT-related fibronectin, E-cadherin, and vimentin protein expression in the IS-treated NRK-52E cells with or without NAC or DFO. Data are presented as means ± SD (n = 6 in (A–D); independent experiments). *, p < 0.05, compared with the control (C) group. #, p < 0.05, compared with the corresponding concentrations of IS groups. One-way ANOVA followed by Tukey’s post hoc test was used to analyze statistical differences.

Journal: Antioxidants (Basel, Switzerland)

Article Title: Inhibition of Indoxyl Sulfate-Induced Reactive Oxygen Species-Related Ferroptosis Alleviates Renal Cell Injury In Vitro and Chronic Kidney Disease Progression In Vivo.

doi: 10.3390/antiox12111931

Figure Lengend Snippet: Figure 2. IS induced ER stress, ferroptosis, and epithelial–mesenchymal transition (EMT) through ROS signaling in the renal tubular cells. NRK-52E cells were treated with various concentrations of IS (0.1–1 mM) for 24 h with or without pretreatment of 1 mM NAC for 1 h or 50 µM deferoxamine (DFO) for 1 h. (A,B) Western blot analysis and quantification for ER stress-related GRP78, p-eIF2α, ATF4, ATF6, and CHOP (A), and ferroptosis-related GPX4, PTGS2, and xCT (B) protein expression. (C) Western blot analysis and quantification for ATF4, CHOP, GPX4, and PTGS2 protein expression in IS-treated NRK-52E cells with or without NAC. (D) Western blot analysis and quantification for EMT-related fibronectin, E-cadherin, and vimentin protein expression in the IS-treated NRK-52E cells with or without NAC or DFO. Data are presented as means ± SD (n = 6 in (A–D); independent experiments). *, p < 0.05, compared with the control (C) group. #, p < 0.05, compared with the corresponding concentrations of IS groups. One-way ANOVA followed by Tukey’s post hoc test was used to analyze statistical differences.

Article Snippet: A normal rat kidney epithelial cell line (NRK-52E) obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA) was used.

Techniques: Western Blot, Expressing, Control