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. 2022 Aug 8;13(8):693. doi: 10.1038/s41419-022-05138-4

Fig. 1. Mice with Gsdmd deficiency had ameliorated renal fibrosis after UUO.

Fig. 1

A Representative images of Masson trichrome staining of kidney sections. Kidneys were isolated from Gsdmd+/+ mice and Gsdmd−/− mice on day 13 after UUO. Scale bar: 100 μm. B Quantification of renal fibrosis scores evaluated by Masson trichrome staining. n = 6. C, E Representative images of immunofluorescence staining of kidney sections, showing the expression of α-smooth muscle actin (α-SMA) C and type-I collagen (Col I) E. DAPI was used for nuclear staining. Scale bar: 100 μm. D, F Quantification of α-SMA D and Col I F expression by immunofluorescence. n = 6. G Western blot analysis for α-SMA and Col I expression of kidney tissue lysates, which were isolated on day 7 and 13 after UUO. GAPDH was used as a loading control. n = 4. H Western blot showing GSDMD cleavage in kidney after UUO. Kidney tissue lysates were isolated on day 0, 7, and 13 after UUO. The knockout efficiency of Gsdmd was also confirmed, and the cleaved GSDMD-N could be observed in WT kidneys. n = 4. **P < 0.01.