Superparamagnetic Iron Oxide Nanoparticles as Magnetic Resonance Imaging Contrast Agents and Induced Autophagy Response in Endothelial Progenitor Cells
Superparamagnetic Iron Oxide Nanoparticles as Magnetic Resonance Imaging Contrast Agents and Induced Autophagy Response in Endothelial Progenitor Cells
复制标题
超顺磁性氧化铁纳米颗粒作为磁共振成像造影剂并诱导内皮祖细胞自噬反应
DOI:
10.1166/jbn.2019.2689
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发表时间:
2019-02-01
影响因子:
2.9
通讯作者:
Guo, Yingkun
中科院分区:
文献类型:
--
作者:
Zhang, Lizhi;Jin, Rongrong;Guo, Yingkun
Endothelial progenitor cells (EPCs) have been used in clinical trials for the treatment of patients with ischemic diseases, such as myocardial infarction and limb ischemia, as they could secrete angiogenic growth factors and promote neovascularization. However, the clinical employment of EPC therapy relies on the establishment of a noninvasive, timely, effective, and safe assessment system. In this study, we recruited superparamagnetic iron oxide nanoparticles (SPION) enhanced magnetic resonance imaging (MRI) to track EPCs in vitro. We evaluated the labeling efficiency of SPION in EPCs without cationic transfection reagents and determined the threshold value of the labeled cell quantity for MRI. Our data suggested that 1x10(5) EPCs incubated with SPION at a concentration of 100 mu g Fe/mL for 24 h could be detected with a clinical 3T MRI T-2 scan. SPION were not cytotoxic for EPCs; however, SPION induced autophagy and impaired neovascularization. We then examined if the impairment could be alleviated through the inhibition of autophagy. The observed autophagy response and its function in EPCs may provide a strategy to improve the safety of SPION labeling. It may also verify that the assessment of autophagy may be a more sensitive detection method to evaluate the biocompatibility of tracking reagents.