<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Kröpfl, J. M.</dc:creator>
  <dc:creator>Spengler, C. M.</dc:creator>
  <dc:creator>Frobert, Aurélien</dc:creator>
  <dc:creator>Ajalbert, Guillaume</dc:creator>
  <dc:creator>Giraud, Marie-Noëlle</dc:creator>
  <dc:date>2018-01-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">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 Peripheral blood was withdrawn and fractional shortening and ejection  fraction of the left ventricle were assessed before (day 0) and 14 days after MI or  sham surgery (day 14).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 &lt; 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 &lt; 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.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306340</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306340/files/gir_mia.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1113/EP086643</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Experimental Physiology. - 2018, vol. 103, no. 1, p. 1–8</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">functional hematopoietic colony count</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">self-renewal ability</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">myocardial infarction</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Myocardial infarction does not affect circulating haematopoietic stem and progenitor cell self‐renewal ability in a rat model</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
