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A Serum creatinine (SCr) and blood urea nitrogen (BUN) levels continuously increased in I/R model mice. n = 6 mice/group. B Temporal expression patterns of <t>chemerin</t> <t>and</t> <t>CMKLR1</t> in the kidneys of I/R model mice. n = 3 (independent experiments). C Quantified data for chemerin and CMKLR1 from the western blots shown in ( B ). D – G Immunofluorescence analysis of chemerin (red; D , F ) expression in the renal cortices. Relative immunofluorescence intensities for chemerin are presented in ( E ) and ( G ), respectively. AQP1 (green; D ) and CK19 (green; F ) were used as markers for renal tubular epithelial cells, and DAPI (blue) was used to stain the nuclei. Scale bar = 100 μm. n = 6 mice/group. Serum chemerin ( H ), blood urea nitrogen (BUN; I ), and creatinine ( J ) levels in healthy individuals and AKI patients. n = 9 humans/group. Spearman correlation analysis between serum chemerin and BUN ( K ) or creatinine ( L ). n = 9 humans/group. M Chemerin expression decreased in nephropathy patients. Data analysis from Nephroseq database ( https://www.nephroseq.org ). Data are presented as the mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. One-way ANOVA with Tukey’s multiple comparison test was used for ( A ) and ( C ), Student’s t test was used for ( E ), ( G )–( J ).
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A Serum creatinine (SCr) and blood urea nitrogen (BUN) levels continuously increased in I/R model mice. n = 6 mice/group. B Temporal expression patterns of chemerin and CMKLR1 in the kidneys of I/R model mice. n = 3 (independent experiments). C Quantified data for chemerin and CMKLR1 from the western blots shown in ( B ). D – G Immunofluorescence analysis of chemerin (red; D , F ) expression in the renal cortices. Relative immunofluorescence intensities for chemerin are presented in ( E ) and ( G ), respectively. AQP1 (green; D ) and CK19 (green; F ) were used as markers for renal tubular epithelial cells, and DAPI (blue) was used to stain the nuclei. Scale bar = 100 μm. n = 6 mice/group. Serum chemerin ( H ), blood urea nitrogen (BUN; I ), and creatinine ( J ) levels in healthy individuals and AKI patients. n = 9 humans/group. Spearman correlation analysis between serum chemerin and BUN ( K ) or creatinine ( L ). n = 9 humans/group. M Chemerin expression decreased in nephropathy patients. Data analysis from Nephroseq database ( https://www.nephroseq.org ). Data are presented as the mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. One-way ANOVA with Tukey’s multiple comparison test was used for ( A ) and ( C ), Student’s t test was used for ( E ), ( G )–( J ).

Journal: Communications Biology

Article Title: Chemerin attenuates acute kidney injury by inhibiting ferroptosis via the AMPK/NRF2/SLC7A11 axis

doi: 10.1038/s42003-024-07377-x

Figure Lengend Snippet: A Serum creatinine (SCr) and blood urea nitrogen (BUN) levels continuously increased in I/R model mice. n = 6 mice/group. B Temporal expression patterns of chemerin and CMKLR1 in the kidneys of I/R model mice. n = 3 (independent experiments). C Quantified data for chemerin and CMKLR1 from the western blots shown in ( B ). D – G Immunofluorescence analysis of chemerin (red; D , F ) expression in the renal cortices. Relative immunofluorescence intensities for chemerin are presented in ( E ) and ( G ), respectively. AQP1 (green; D ) and CK19 (green; F ) were used as markers for renal tubular epithelial cells, and DAPI (blue) was used to stain the nuclei. Scale bar = 100 μm. n = 6 mice/group. Serum chemerin ( H ), blood urea nitrogen (BUN; I ), and creatinine ( J ) levels in healthy individuals and AKI patients. n = 9 humans/group. Spearman correlation analysis between serum chemerin and BUN ( K ) or creatinine ( L ). n = 9 humans/group. M Chemerin expression decreased in nephropathy patients. Data analysis from Nephroseq database ( https://www.nephroseq.org ). Data are presented as the mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. One-way ANOVA with Tukey’s multiple comparison test was used for ( A ) and ( C ), Student’s t test was used for ( E ), ( G )–( J ).

Article Snippet: The primary antibodies used were: Chemerin (sc-373797; Santa Cruz Biotechnology, USA; 1:500), CMKLR1 (SC-398769; Santa Cruz Biotechnology, USA; 1:500), TNFα (60291-1-Ig; Proteintech, USA; 1:500), IL-6 (21865-1-AP; Proteintech, USA; 1:500), ACSL4 (22401-1-AP; Proteintech, USA; 1:500), GPX4 (67763-1-Ig; Proteintech, USA; 1:500), SLC7A11 (ab175186; Abcam, USA; 1:500), p-NRF2 (PA5-67520; Invitrogen, USA; 1:200), NRF2 (80593-1-RR; Proteintech, USA; 1:500), AQP1 (ab168387; Abcam, USA; 1:500), and Cytokeratin 19 (CK19; 60187-lg; Proteintech, USA; 1:500).

Techniques: Expressing, Western Blot, Immunofluorescence, Staining, Comparison