TY - JOUR
T1 - In oxine labelled mesenchymal stem cell spect after intravenous administration in myocardial infarction
AU - Chin, B. B.
AU - Nakamoto, Y.
AU - Bulte, J. W.M.
AU - Pittenger, M. F.
AU - Wahl, R.
AU - Kraitchman, D. L.
PY - 2003/11
Y1 - 2003/11
N2 - Mesenchymal stem cells (MSCs) have shown therapeutic potential if successfully delivered to the intended site of myocardial infarction. The purpose of this pilot study was to test the feasibility of In oxine labelling of MSCs and single photon emission computed tomography (SPECT) imaging after intravenous administration in a porcine model of myocardial infarction. Adult farm pigs (n = 2) were subjected to closed chest experimental myocardial infarction. In oxine labelled MSCs (1×10 to 2×10 cells) were infused intravenously, and SPECT imaging was performed initially and on days 1, 2, 7 and 14. High quality SPECT images were obtained through 2 weeks of imaging. High initial MSC localization occurred in the lungs and slow progressive accumulation occurred in the liver, spleen and bone marrow. Renal activity was mild and persistent throughout imaging. No appreciable accumulation occurred in the myocardium. It is concluded that In oxine radiolabelling of MSCs is feasible, and in vivo imaging with SPECT provides a non-invasive method for sequentially monitoring cell trafficking with good spatial resolution. Because intravenous administration of MSCs results in significant lung activity that obscures the assessment of myocardial cell trafficking, alternative routes of administration should be investigated for this application.
AB - Mesenchymal stem cells (MSCs) have shown therapeutic potential if successfully delivered to the intended site of myocardial infarction. The purpose of this pilot study was to test the feasibility of In oxine labelling of MSCs and single photon emission computed tomography (SPECT) imaging after intravenous administration in a porcine model of myocardial infarction. Adult farm pigs (n = 2) were subjected to closed chest experimental myocardial infarction. In oxine labelled MSCs (1×10 to 2×10 cells) were infused intravenously, and SPECT imaging was performed initially and on days 1, 2, 7 and 14. High quality SPECT images were obtained through 2 weeks of imaging. High initial MSC localization occurred in the lungs and slow progressive accumulation occurred in the liver, spleen and bone marrow. Renal activity was mild and persistent throughout imaging. No appreciable accumulation occurred in the myocardium. It is concluded that In oxine radiolabelling of MSCs is feasible, and in vivo imaging with SPECT provides a non-invasive method for sequentially monitoring cell trafficking with good spatial resolution. Because intravenous administration of MSCs results in significant lung activity that obscures the assessment of myocardial cell trafficking, alternative routes of administration should be investigated for this application.
KW - Cell trafficking
KW - In oxine
KW - Mesenchymal stem cells
KW - Myocardial infarction
KW - Single photon emission tomography
UR - http://www.scopus.com/inward/record.url?scp=9344238503&partnerID=8YFLogxK
U2 - 10.1097/00006231-200311000-00005
DO - 10.1097/00006231-200311000-00005
M3 - Article
C2 - 14569169
AN - SCOPUS:9344238503
VL - 24
SP - 1149
EP - 1154
JO - Nuclear Medicine Communications
JF - Nuclear Medicine Communications
SN - 0143-3636
IS - 11
ER -