[Expression of SDF-1/CXCR4 in acute infarct myocardium after implantation of bone marrow mesenchymal stem cells in rats]

Zhonghua Yi Xue Za Zhi. 2015 May 12;95(18):1421-4.
[Article in Chinese]

Abstract

Objective: To explore the role of stromal cell derived factor-1 (SDF-1)/CXCR4 axis in acute infarct myocardium after an implantation of bone marrow mesenchymal stem cells (MSCs) in rats.

Methods: The animals were anesthetized by an intraperitoneal injection of pentobarbital sodium. Left anterior thoracotomy through 3/4 intercostals region was performed and then left anterior descending coronary arteries were ligated for modeling acute myocardial infarction. The MSCs were injected into the area of acute infarct myocardium after a 10-minute ligation of left anterior descending coronary artery. The different concentration and expression of SDF-1/CXCR4 in the area of acute myocardial infarction and left ventricular function were analyzed.

Results: At day 28 post-transplantation, the vascular density in MSCs implant group were significantly higher than that in control group (P<0.05). And left ventricular function in MSCs implant group improved significantly than that in control group too (P<0.05). At the same time, the expressions of SDF-1 and CXCR4 in topical injection sites of infarct myocardium were significantly higher than those in control group (P<0.05). In MSCs implant group, the level of SDF-1/CXCR4 peaked at Day 1 post-transplantation and then it declined.

Conclusions: After the implantation of MSCs into acute infarct myocardium, there is vascular regeneration and the level of SDF-1/CXCR4 increases so that left ventricular function improves. And the mechanism may be due to an up-regulation of SDF-1/CXCR4 axis.

MeSH terms

  • Animals
  • Bone Marrow Cells*
  • Hematopoietic Stem Cells
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells*
  • Myocardial Infarction*
  • Myocardium
  • Rats
  • Receptors, CXCR4
  • Regeneration
  • Signal Transduction
  • Up-Regulation
  • Ventricular Function, Left

Substances

  • Cxcr4 protein, rat
  • Receptors, CXCR4