TY - JOUR
T1 - Comparison of transplantation of adipose tissue- and bone marrow-derived mesenchymal stem cells in the infarcted heart
AU - Van Der Bogt, Koen E.A.
AU - Schrepfer, Sonja
AU - Yu, Jin
AU - Sheikh, Ahmad Y.
AU - Hoyt, Grant
AU - Govaert, Johannes A.
AU - Velotta, Jeffrey B.
AU - Contag, Christopher H.
AU - Robbins, Robert C.
AU - Wu, Joseph C.
PY - 2009/3/15
Y1 - 2009/3/15
N2 - Background. Mesenchymal stem cells hold promise for cardiovascular regenerative therapy. Derivation of these cells from the adipose tissue might be easier compared with bone marrow. However, the in vivo fate and function of adipose stromal cells (ASC) in the infarcted heart has never been compared directly to bone marrow-derived mesenchymal cells (MSC). Methods. ASC and MSC were isolated from transgenic FVB mice with a β-actin promoter driving firefly luciferase and green fluorescent protein double fusion reporter gene, and they were characterized using flow cytometry, microscopy, bioluminescence imaging and luminometry. FVB mice (n=8 per group) underwent myocardial infarction followed by intramyocardial injection of 5×10 5 ASC, MSC, fibroblasts (Fibro, positive control), or saline (negative control). Cell survival was measured using bioluminescence imaging for 6 weeks and cardiac function was monitored by echocardiography and pressure-volume analysis. Ventricular morphology was assessed using histology. Results. ASC and MSC were CD34 -, CD45 -, c-Kit -, CD90 +, Sca-1 +, shared similar morphology and had a population doubling time of ∼2 days. Cells expressed Fluc reporter genes in a number-dependent fashion as confirmed by luminometry. After cardiac transplantation, both cell types showed drastic donor cell death within 4 to 5 weeks. Furthermore, transplantation of either cell type was not capable of preserving ventricular function and dimensions, as confirmed by pressure-volume-loops and histology. Conclusion. This is the first study comparing the in vivo behavior of both cell types in the infarcted heart. ASC and MSC do not tolerate well in the cardiac environment, resulting in acute donor cell death and a subsequent loss of cardiac function similar to control groups.
AB - Background. Mesenchymal stem cells hold promise for cardiovascular regenerative therapy. Derivation of these cells from the adipose tissue might be easier compared with bone marrow. However, the in vivo fate and function of adipose stromal cells (ASC) in the infarcted heart has never been compared directly to bone marrow-derived mesenchymal cells (MSC). Methods. ASC and MSC were isolated from transgenic FVB mice with a β-actin promoter driving firefly luciferase and green fluorescent protein double fusion reporter gene, and they were characterized using flow cytometry, microscopy, bioluminescence imaging and luminometry. FVB mice (n=8 per group) underwent myocardial infarction followed by intramyocardial injection of 5×10 5 ASC, MSC, fibroblasts (Fibro, positive control), or saline (negative control). Cell survival was measured using bioluminescence imaging for 6 weeks and cardiac function was monitored by echocardiography and pressure-volume analysis. Ventricular morphology was assessed using histology. Results. ASC and MSC were CD34 -, CD45 -, c-Kit -, CD90 +, Sca-1 +, shared similar morphology and had a population doubling time of ∼2 days. Cells expressed Fluc reporter genes in a number-dependent fashion as confirmed by luminometry. After cardiac transplantation, both cell types showed drastic donor cell death within 4 to 5 weeks. Furthermore, transplantation of either cell type was not capable of preserving ventricular function and dimensions, as confirmed by pressure-volume-loops and histology. Conclusion. This is the first study comparing the in vivo behavior of both cell types in the infarcted heart. ASC and MSC do not tolerate well in the cardiac environment, resulting in acute donor cell death and a subsequent loss of cardiac function similar to control groups.
KW - Adipose stromal cells
KW - Bone marrow stem cells
KW - Mesenchymal stem cells
KW - Molecular imaging
KW - Myocardial infarction
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U2 - 10.1097/TP.0b013e31819609d9
DO - 10.1097/TP.0b013e31819609d9
M3 - Article
C2 - 19295307
AN - SCOPUS:63049092214
SN - 0041-1337
VL - 87
SP - 642
EP - 652
JO - Transplantation
JF - Transplantation
IS - 5
ER -