Mesoangioblasts, Vessel-Associated Multipotent Stem Cells, Repair the Infarcted Heart by Multiple Cellular Mechanisms
Mesoangioblasts, Vessel-Associated Multipotent Stem Cells, Repair the Infarcted Heart by Multiple Cellular Mechanisms
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中成血管细胞、血管相关多能干细胞通过多种细胞机制修复梗塞心脏
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发表时间:
2005
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通讯作者:
RobertoLatini
中科院分区:
文献类型:
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作者:
DanielaGalli;AnnaInnocenzi;LidiaStaszewsky;LuciaZanetta;MaurilioSampaolesi;AntonioBai;ElenaMartinoli;EleonoraCarlo;GiovannaBalconi;FabioFiordaliso;StefanoChimenti;GabriellaCusella;ElisabettaDejana;GiulioCossu;RobertoLatini
Objective— To test the potential of mesoangioblasts (Mabs) in reducing postischemic injury in comparison with bone marrow progenitor cells (BMPCs), fibroblasts (Fbs), and embryonic stem cell–derived endothelial cells (ECs), and to identify putative cellular protective mechanisms. Methods and Results— Cells were injected percutaneously in the left ventricular (LV) chamber of C57BL/6 mice, 3 to 6 hours after coronary ligation, and detected in the hearts 2 days and 6 weeks later. Echocardiographic examinations were performed at 6 weeks. LV dilation was reduced and LV shortening fraction was improved with Mabs and BMPCs but not with ECs and Fbs. Donor cell colonization of the host myocardium was modest and predominantly in the smooth muscle layer of vessels. Capillary density was higher in the peripheral infarct area and apoptotic cardiomyocytes were fewer with Mabs and BMPCs. Mabs and BMPCs, but not Fbs or ECs, promoted survival of cultured cardiocytes under low-oxygen in culture. This activity was present i...