|Mobilization of CD34/CXCR4+, CD34/CD117+, c-met+ stem cells, and mononuclear cells expressing early cardiac, muscle, and endothelial markers into peripheral blood in patients with acute myocardial infarction.|
|PMID: 15533859 Owner: NLM Status: MEDLINE|
|BACKGROUND: Adult stem cells can contribute to myocardial regeneration after ischemic injury. Bone marrow and skeletal muscles contain a population of CXCR4+ cells expressing genes specific for muscle progenitor cells that can be mobilized into the peripheral blood. The aims of the study were (1) to confirm the presence of early tissue-committed cells expressing cardiac, muscle, and endothelial markers in populations of mononuclear cells in peripheral blood and (2) to assess the dynamics and magnitude of the mobilization of CD34+, CD117+, CXCR4+, c-met+, CD34/CD117+, and CD34/CXCR4+ stem cells into peripheral blood in relation to inflammatory and hematopoietic cytokines in patients with ST-segment-elevation acute myocardial infarction (STEMI). METHODS AND RESULTS: Fifty-six patients with STEMI (<12 hours), 39 with stable angina, and 20 healthy control subjects were enrolled. Real-time reverse transcription-polymerase chain reaction (RT-PCR) was used for detection of tissue-specific markers. The number of the cells was assessed by use of a flow cytometer on admission, after 24 hours, and after 7 days. RT-PCR revealed increased expression of mRNA (up to 3.5-fold increase) for specific cardiac (GATA4, MEF2C, Nkx2.5/Csx), muscle (Myf5, Myogenin, MyoD), and endothelial (VE-cadherin, von Willebrand factor) markers in peripheral blood mononuclear cells. The number of CD34/CXCR4+ and CD34/CD117+ and c-met+ stem cells in peripheral blood was significantly higher in STEMI patients than in stable angina and healthy subjects, peaking on admission, without further significant increase after 24 hours and 7 days. CONCLUSIONS: The study demonstrates in the setting of STEMI a marked mobilization of mononuclear cells expressing specific cardiac, muscle, and endothelial markers as well as CD34/CXCR4+ and CD34/CD117+ and c-met+ stem cells and shows that stromal cell-derived factor-1 is an important factor influencing the mobilization.|
|Wojciech Wojakowski; Michał Tendera; Anna Michałowska; Marcin Majka; Magdalena Kucia; Katarzyna Maślankiewicz; Rafał Wyderka; Andrzej Ochała; Mariusz Z Ratajczak|
Related Documents :
|24073229 - Ectopic expression of nolz-1 in neural progenitors promotes cell cycle exit/premature n...
18816169 - New source of muscle-derived stem cells with potential for alveolar bone reconstruction...
24101189 - The role of mesenchymal stem cells in bone repair and regeneration.
17190299 - Cell-based bone reconstruction therapies-principles of clinical approaches.
17506689 - The role of pax genes in the development of tissues and organs: pax3 and pax7 regulate ...
23495139 - Autophagic control of cell 'stemness'
7671999 - Sigma binding site ligands inhibit cell proliferation in mammary and colon carcinoma ce...
9916699 - Role of bcl-2 in alpha beta t cell development in mice deficient in the common cytokine...
300179 - Peripheral lymphocyte count and suppopulations of t and b lymphocytes in benign and mal...
|Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't Date: 2004-11-08|
|Title: Circulation Volume: 110 ISSN: 1524-4539 ISO Abbreviation: Circulation Publication Date: 2004 Nov|
|Created Date: 2004-11-16 Completed Date: 2005-06-15 Revised Date: 2009-11-19|
Medline Journal Info:
|Nlm Unique ID: 0147763 Medline TA: Circulation Country: United States|
|Languages: eng Pagination: 3213-20 Citation Subset: AIM; IM|
|Third Division of Cardiology, Silesian School of Medicine, 45-47 Ziołowa St, 40-635 Katowice, Poland. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Angina Pectoris / blood, physiopathology
Antigens, CD34 / analysis
Antigens, Differentiation / analysis*
Blood Cell Count
Chemokines, CXC / blood, physiology
Cytokines / blood*
Endothelium / cytology
Granulocyte Colony-Stimulating Factor / blood
Hepatocyte Growth Factor / blood
Inflammation / blood
Interleukin-6 / blood
Leukocytes, Mononuclear / chemistry, physiology*
Multipotent Stem Cells / chemistry, physiology*
Muscles / cytology
Myocardial Infarction / blood*, physiopathology
Myocardium / cytology
Proto-Oncogene Proteins c-kit / analysis
Proto-Oncogene Proteins c-met / analysis
Receptors, CXCR4 / analysis
Reverse Transcriptase Polymerase Chain Reaction
Vascular Endothelial Growth Factor A / blood
|0/Antigens, CD34; 0/Antigens, Differentiation; 0/CXCL12 protein, human; 0/Chemokine CXCL12; 0/Chemokines, CXC; 0/Cytokines; 0/Interleukin-6; 0/Receptors, CXCR4; 0/Vascular Endothelial Growth Factor A; 143011-72-7/Granulocyte Colony-Stimulating Factor; 67256-21-7/Hepatocyte Growth Factor; EC 184.108.40.206/Proto-Oncogene Proteins c-kit; EC 220.127.116.11/Proto-Oncogene Proteins c-met|
Circulation. 2005 May 24;111(20):e307; author reply e307-8
Circulation. 2004 Nov 16;110(20):3158-60 [PMID: 15545526 ]
Circulation. 2005 May 24;111(20):e307-8; author reply e307-8 [PMID: 15911712 ]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Upregulation of myocardial estrogen receptors in human aortic stenosis.
Next Document: Assessment of systemic right ventricular function in patients with transposition of the great arteri...