Absence of myocyte regeneration by mobilization of bone marrow stem cells after myocardial infarction.

The study aimed to test the potential for bone marrow stem cells (BMSC) mobilized by granulocyte macrophage colony stimulating factor (GM-CSF) to promote neovascularization and cardiomyocytes regeneration in a rat model of myocardial infarction. The myocardial infracted rats were randomly assigned to receive GM-CSF injection as GM-CSF group or received saline injection as control group. Evaluation of CD34 stem cells was performed by flow cytometry.

[Effects of mobilization of bone marrow stem cells on regenerative potential of cardiac tissues after myocardial infarction].

Objective: To test the potential of bone marrow stem cells mobilized by granulocyte macrophage colony stimulating factor (GM-CSF) to promote regeneration of myocyte and neovascularization in a rat model of myocardial infarction.

Methods: A myocardial infarction model was created by ligation of the left anterior descending coronary artery in adult Sprague-Dawley rats. Then the infracted rats were randomly assigned to receive GM-CSF injection subcutaneously 50 microg x kg(-1) x day(-1) as experimental group or receive saline injection as control group.

Is it possible to obtain "true endothelial progenitor cells" by in vitro culture of bone marrow mononuclear cells?

In vitro-cultured bone marrow cells have been shown to contain some low-density lipoprotein (LDL) uptake-positive cells. Although a small portion of LDL uptake-positive cells had expression for endothelial markers, all of them demonstrated a phagocytosis function similar to monocyte/macrophages and expression of the panleukocyte surface marker CD45 and monocyte marker CD14. These LDL uptake-positive cells did not show significant proliferative capacity and died out gradually in long-term culture.

Transplantation of mesenchymal stem cells from human bone marrow improves damaged heart function in rats.

Background: Bone marrow-derived mesenchymal stem cells (MSCs) are of great therapeutic potential after myocardial ischemic injury. However, little is known about the biological characteristics of MSCs in patients with coronary artery disease and their effects on infracted myocardium. The present study evaluated the biological characteristics of MSCs from patients with coronary artery disease and their effects after being transplanted into infarcted myocardium using a rat model.

Adult endothelial progenitor cells from human peripheral blood maintain monocyte/macrophage function throughout in vitro culture.

Mononuclear cells (MNCs) isolated from peripheral blood by density gradient centrifugation were plated on human fibronectin-coated culture plates and cultured in EGM-2 medium. Attached spindle-shaped cells, reported as endothelial progenitor cells (EPCs) by some investigators, had elongated from adherent round cells, but had not proliferated from a small number of cells as supposed previously. The growth curve of the primary EPCs showed that the cells had little proliferative capacity.