Myocardial infarction does not affect circulating haematopoietic stem and progenitor cell self‐renewal ability in a rat model

• Published in: Experimental physiology Vol. 103; no. 1; pp. 1 - 8
• Main Authors: Kröpfl, J. M., Spengler, C. M., Frobert, A., Ajalbert, G., Giraud, M. N.
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.01.2018
• Subjects: Animals; Cell Self Renewal - physiology; Cell self-renewal; Cell Separation - methods; Coronary artery; Disease Models, Animal; Female; functional hematopoietic colony count; Hematopoietic stem cells; Hematopoietic Stem Cells - physiology; Macrophages; myocardial infarction; Myocardial Infarction - blood; Myocardial Infarction - physiopathology; Progenitor cells; Rats; Rats, Inbred Lew; self‐renewal ability; self-renewal ability; functional hematopoietic colony count; myocardial infarction
• ISSN: 0958-0670; 1469-445X
• DOI: 10.1113/EP086643

New Findings What is the central question of this study? Although peripheral blood haematopoietic stem and progenitor cells are potentially important in regeneration after acute myocardial infarction, their self‐renewal ability in the post‐acute phase has not yet been addressed. What is the main finding and its importance? In rat peripheral blood, we show that myocardial infarction does not negatively affect circulating haematopoietic stem and progenitor cell self‐renewal ability 2 weeks after acute infarction, which suggests a constant regenerative potential in the myocardial infarction post‐acute phase. Given the importance of peripheral blood haematopoietic stem and progenitor cells (HPCs) in post‐acute regeneration after acute myocardial infarction (MI), the aim of the present study was to investigate the number and secondary replating capacity/self‐renewal ability of HPCs in peripheral blood before and 2 weeks after MI. In female Lewis inbred rats (n = 9), MI was induced by ligation of the left coronary artery, and another nine underwent sham surgery, without ligation, for control purposes. Myocardial infarction was confirmed by troponin I concentrations 24 h after surgery. Peripheral blood was withdrawn and fractional shortening and ejection fraction of the left ventricle were assessed before (day 0) and 14 days after MI or sham surgery (day 14). After mononuclear cell isolation, primary and secondary functional colony‐forming unit granulocyte–macrophage (CFU‐GM) assays were performed in order to detect the kinetics of functional HPC colony counts and cell self‐renewal ability in vitro. The CFU‐GM counts and cell self‐renewal ability remained unchanged (P > 0.05) in both groups at day 14, without interaction between groups. In the intervention group, higher day 0 CFU‐GM counts showed a relationship to lower fractional shortening on day 14 (ρ = −0.82; P < 0.01). Myocardial infarction did not negatively affect circulating HPC self‐renewal ability, which suggests a constant regenerative potential in the post‐acute phase. A relationship of cardiac contractile function 14 days after MI with circulating CFU‐GM counts on day 0 might imply functional colony count as a predictive factor for outcome after infarction.