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. 2024 Nov 8;15:9667. doi: 10.1038/s41467-024-53564-z

Fig. 3. Cardiac-specific FNDC4 knockdown inhibits cardiomyocyte survival and angiogenesis during cardiac I/R injury.

Fig. 3

a Evans blue and TTC double staining was performed to identify the IA, AAR and remote area of heart samples 24 h after I/R surgery (n = 6). b Heart samples with or without FNDC4 knockdown were collected 24 h after I/R surgery and subjected to TUNEL staining, and TUNEL+ nuclei were quantified. Arrows indicate TUNEL+ nuclei (n = 6). c–e Heart samples with or without FNDC4 knockdown were collected 4 weeks after I/R surgery and subjected to immunofluorescence staining, and the numbers of capillaries as well as arterioles were quantified. Arrows indicate α-SMA+ arterioles (n = 6). f, g Heart samples with or without FNDC4 knockdown were collected 4 weeks after I/R surgery and subjected to HE and PSR staining, and cell size as well as fibrotic area were quantified. Circles indicate the cross-sectional area of cardiomyocytes (n = 6). h Cardiac function of FNDC4-silenced and control mice was analyzed by transthoracic echocardiography at the indicated time points (n = 6). Data were presented as the mean ± S.D., and analyzed using an unpaired two-tailed Student′s t-test. For the analysis in (f, g), one-way ANOVA followed by Tukey post hoc test was used. For the analysis in (h), repeated measures ANOVA was performed. *P < 0.0001. Source data are provided as a Source Data file.