Cardiomyocyte specific CD38 deletion protects heart from acute myocardial infarction by activating Sirt3 signaling pathway

Sci Rep. 2025 May 17;15(1):17165. doi: 10.1038/s41598-025-02207-4.

Abstract

Acute myocardial infarction (AMI) is serious disease with high morbidity and mortality worldwide. CD38 is an important metabolic enzyme and plays an important role in a variety of diseases. Our previous studies demonstrated that CD38 deficiency significantly reduced Ang-II-induced ventricular hypertrophy and cardiac ischemia-reperfusion injury. However, the roles of cardiomyocytic CD38 in acute myocardial infarction (AMI) remain unknown. Here, we reported that cardiomyocyte-specific CD38 deficiency (CD38CKO) significantly improved heart functions in AMI. We observed that CD38CKO remarkably reduced the fibrosis at the peri-infarct area, and inhibited the apoptosis of cardiomyocytes in infarcted area by elevating the ratio of mitochondrial Bcl2/Bax expression and increased the expressions of the mitochondrial fusion proteins Mfn1 and Mfn2 in the early stage of AMI. Consistently, knockdown of CD38 protected hypoxia-induced apoptosis in cardiomyocytes by increasing the ratio of Bcl2/Bax expression and decreasing cleaved caspase-3. More importantly, 3-TYP, a Sirt3 inhibitor, significantly increased hypoxia-induced apoptosis in CD38-deficient primary cardiomyocytes. In conclusion, our results demonstrated that CD38CKO suppressed apoptosis of cardiomyocytes in the infracted area of heart via activating NAD+/Sirt3-mediated signaling pathways.

Keywords: Apoptosis; CD38; Cardiomyocytes; Mitochondria; Sirt3.

MeSH terms

  • ADP-ribosyl Cyclase 1* / deficiency
  • ADP-ribosyl Cyclase 1* / genetics
  • ADP-ribosyl Cyclase 1* / metabolism
  • Animals
  • Apoptosis
  • Male
  • Membrane Glycoproteins* / deficiency
  • Membrane Glycoproteins* / genetics
  • Membrane Glycoproteins* / metabolism
  • Mice
  • Mice, Knockout
  • Myocardial Infarction* / genetics
  • Myocardial Infarction* / metabolism
  • Myocardial Infarction* / pathology
  • Myocytes, Cardiac* / metabolism
  • Myocytes, Cardiac* / pathology
  • Signal Transduction*
  • Sirtuin 3* / metabolism
  • bcl-2-Associated X Protein / metabolism

Substances

  • ADP-ribosyl Cyclase 1
  • Sirtuin 3
  • Sirt3 protein, mouse
  • Cd38 protein, mouse
  • Membrane Glycoproteins
  • bcl-2-Associated X Protein