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. 2022 Jun 3;7:171. doi: 10.1038/s41392-022-00971-7

Fig. 7.

Fig. 7

The BCAA catabolic capability of ADSCs determined their adaptation and cardioprotective efficacy in the post-infarction heart. a Retention of ADSCs labeled by the cell tracker CM-DiI (red) was visualized by immunostaining of heart tissues 1, 3, and 7 d post-MI. Troponin T staining (green) indicates cardiomyocytes. Left panel, representative images; right panel, ratios of the number of engrafted ADSCs to the number of cardiomyocytes. ADSC-Ctrl ADSCs transfected with adenovirus carrying empty plasmids, ADSC-PP2Cm ADSCs transfected with adenovirus overexpressing PP2Cm, ADSC-BCKDK ADSCs transfected with adenovirus overexpressing BCKDK. b Top panel, representative echocardiographic images 28 d post-MI; bottom panel, quantification of LVEF at baseline and 7, 14, and 28 d after MI. c Representative images of TUNEL staining (top) and CD31 immunostaining in the infarct border zone 3-d post-MI (middle). Bottom panel, quantification of TUNEL and CD31 staining intensity. d Left panel, representative images of Masson’s trichrome stained tissue from the bottom to the apex of hearts 28 d post-MI. right panel, quantification values of infarcted area as determined with ImageJ software. e HW/BW ratios 28 d post-MI; f LW/BW ratios 28 d post-MI. The data are shown as the means ± SD. Data were analysed by one-way ANOVA followed by a Bonferroni post hoc test. ADSCs adipose tissue-derived mesenchymal stem cells, AutoFluo autofluorescence, BCAA branched-chain amino acids, BCKDK BCKDHA kinase, HW/BW heart weight/body weight ratio, LW/BW lung weight/body weight ratio, MI myocardial infarction, PP2Cm mitochondrial matrix-targeted protein phosphatase 2C family member, TUNEL transferase-mediated dUTP nick-end labeling