Meeting Banner
Abstract #4365

MR Contrast and Biological Impacts of Intracellular Superparamagnetic Iron Oxides on Human Mesenchymal Stem Cells with Hypoxic Ischemic Exposure

Jens T. Rosenberg1, 2, Katelyn Sellgren2, Michelle A. Baird, Micheal W. Davidson, 3, Teng Ma2, Samuel Colles Grant1, 2

1Center for Interdisciplinary Magnetic Resonance, The National High Magnetic Field Laboratory, Tallahassee, FL, United States; 2Chemical & Biomedical Engineering, The Florida State University, Tallahassee, FL, United States; 3Department of Biological Science, The Florida State University, Tallahassee, FL, United States

Labeling of human mesenchymal stem cells (hMSCs) with superparamagnetic iron oxides (SPIOs) have been demonstrated but few studies have investigated biological impacts or long term tracking capability, especially under stroke conditions. This study shows that hMSCs display dose dependent SPIO uptake and progressive decreases in contrast over extended culture mimicking the maximum expected transplant duration. Though other biological effects were impacted minimally by SPIOs, hypoxic ischemic conditions increased cytotoxicity significantly, with vulnerability related to SPIO exposure. This finding needs to be considered when introducing intracellular contrast agents for cellular based regenerative therapies in an ischemic, low oxygen environment.

Keywords

ability afterward agents animal arterially artery best beyond biological biomedical blue calcium cancer cell cells challenge chemical college colony comp condition conditions console contrast control created culture damage dashed days death derived determined dings division dose doses ease engineering engulf engulfed enhancing equal equipped ester expo exposed exposure exposures expression extended fashion field finding form funding furthermore gained gene gradients green grow hand harvested head hemisphere highest histology human impact impacts implants in vivo incubation indicated indicating induction inhibited initial initially injected injection intracellular investigate iron labeled laboratory layered load loadings localization located long macrophage magnet marrow medium microscopic middle mimic ming minim mixed model must neuronal norm nuclear nuclei nutrient occlusion period permanence plates potential presence prevalent prime proliferation rang rats readily reduces regulated resolution respective reveal sacrificed science secrete serum significantly solid spin statistical stem stroke tagged term therapies though tissue toxicity track tracking unlabeled uptake user valuation vitro voids washed