Blocking the A2B adenosine receptor alleviates myocardial damage by inhibiting spleen-derived MDSC mobilisation after acute myocardial infarction

Background Myeloid-derived suppressor cell (MDSC) mobilisation is an important immune event in acute myocardial infarction (AMI). The A(2B) adenosine receptor (A(2B)AR) plays key role in regulating MDSC function, but its specific involvement in MDSC mobilisation in AMI remains unclear. Methods In AMI patients, the circulating MDSC ratio and A(2B)AR mRNA expression were measured. A mouse AMI model was established by left anterior descending coronary artery (LADCA) ligation. MDSCs were analysed by FACS and immunofluorescence staining (of heart tissue). A(2B)AR mRNA expression was assessed by qRT-PCR. Myocardial injury was detected by HE staining. Myocardial cell apoptosis was analysed by immunohistochemistry. Cardiac systolic function was evaluated by transthoracic echocardiography. Results In AMI patients, the circulating MDSC ratio was increased and positively correlated with A(2B)AR mRNA expression (r = 0.86, p < 0.01). In AMI model mice, the percentage of MDSCs was increased in the circulation and infarcted heart and decreased in the spleen. MRS-1754-mediated A(2B)AR inhibition decreased the MDSC ratio in the circulation and infarcted heart and prevented the decrease in MDSC number in the spleens of mice with AMI. A(2B)AR blockade inhibited myocardial cell apoptosis, alleviated myocardial inflammatory injury, and improved myocardial systolic function in the AMI mouse model. Similar results were found in mice after splenectomy. Additionally, spleen-derived MDSC injection increased the MDSC ratio in the infarcted heart, increased myocardial cell apoptosis, aggravated myocardial injury, and decreased cardiac systolic function in mice with AMI. Conclusion Blocking A(2B)AR alleviates myocardial damage and improves myocardial systolic function through inhibition of spleen-derived MDSC mobilisation after AMI. Key Messages Spleen-derived MDSC mobilisation aggravates myocardial inflammatory injury within 24 h of AMI. A(2B)AR promotes spleen-derived MDSC mobilisation within 24 h of AMI. Blocking A(2B)AR improves myocardial systolic function through inhibition of spleen-derived MDSC mobilisation.

Automated summary

Blocking A(2B)AR alleviates myocardial damage and improves myocardial systolic function through inhibition of spleen-derived MDSC mobilisation after AMI. Spleen-derived MDSC mobilisation aggravates myocardial inflammatory injury within 24 h of AMI. A(2B)AR promotes spleen-derived MDSC mobilisation within 24 h of AMI. Blocking A(2B)AR improves myocardial systolic function through inhibition of spleen-derived MDSC mobilisation.