Myocardial CD34+ Stromal Cells/Telocytes Demonstrate a Dynamic Pattern of Interactions with CD68+ Macrophages During Post-Myocardial Infarction Healing

Abstract

Introduction: Myocardial CD34-positive (+) stromal cells/telocytes (SC/TCs) have been recently recognized as a novel type of resident cells involved in post-myocardial infarction (MI) repair. Alternatively, CD68-positive (+) macrophages are well-known constituents in this process. However, the relationship between these two cell populations remains mostly obscure. Therefore, this study was aimed to determine whether resident CD34+ SC/TCs and phagocytic CD68+ macrophages have any evident pattern of interactions during the inflammatory and proliferative phases of post-MI scar formation. Methods: A large transmural MI was induced in middle-aged male Sprague-Dawley rats (n = 15) under ketamine and xylazine anesthesia by permanent ligation of the left anterior descending coronary artery. The post-MI rats were infused with BrdU (5-bromo-2'-deoxyuridine) in a dose of 12.5 mg/kg/day for 72 hours via intraperitoneal osmotic minipumps on day 0, 4, or 11 after surgery. The rats were euthanized on day 3, 7 and 14 after MI, and their hearts were processed for histology and immunostaining. Results: On the third day after MI, CD34+ SC/TCs and CD68+ macrophages were absent within the core of the necrotic tissue, whereas both types of cells were juxtaposed in the space surrounding the area of coagulative necrosis. Furthermore, the presence of BrdU labeling in the nuclei of numerous CD34+ SC/TCs suggests their proliferation in the region of the active macrophage clearing. On the seventh day after MI, CD68+ macrophages were observed to have had advanced toward the center of the necrotic region leaving behind the area occupied primarily with acellular basement membranes from the resorbed CMs, whereas most of CD34+ SC/TCs trailed slightly behind. In part, such delay in centripetal progression of CD34+ SC/TCs through the areas of resorption could be attributed to the fact that these cells, in contrast to macrophages, often migrated along the acellular basement membranes left from the dead CMs that required phagocytic removal of necrotic debris to occur first. On the fourteenth day after MI, the population of CD68+ cells appeared notably reduced and demonstrated a patchy distribution predominantly along the remnants of the necrotic tissue. Meanwhile, the substantially expanded population of CD34+ SC/TCs were observed throughout the entire transmural scar, excluding the areas containing dead “mummified” CMs, aggregates of myofibroblasts and the fibroelastic thickening in subepicardial and subendocardial regions. Conclusion: Our findings, for the first time, demonstrate that populations of resident CD34+ SC/TCs and phagocytic CD68+ macrophages exhibit a dynamic pattern of interactions during early phases of post-MI scar formation, suggesting their importance in the process of post-ischemic myocardial healing. Supported by Camden Health Research Initiative. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.