活力测定
间质细胞
胚胎干细胞
骨髓
生物发光成像
体内
干细胞
化学
病理
细胞
细胞培养
细胞生物学
生物
医学
转染
生物化学
荧光素酶
遗传学
生物技术
基因
作者
Mayumi Yamada,Paul T. Gurney,Jaehoon Chung,Pratima Kundu,Micha Drukker,Alan K. Smith,Irving L. Weissman,Dwight G. Nishimura,Robert C. Robbins,Phillip C. Yang
摘要
Abstract This study investigated the ability of MnCl 2 as a cellular MRI contrast agent to determine the in vitro viability of human embryonic stem cells (hESC) and human bone marrow stromal cells (hBMSC). Basic MRI parameters including T 1 and T 2 values of MnCl 2 ‐labeled hESC and hBMSC were measured and viability signal of manganese (Mn 2+ )‐labeled cells was validated. Furthermore, the biological activity of Ca 2+ ‐channels was modulated utilizing both Ca 2+ ‐channel agonist and antagonist to evaluate concomitant signal changes. Metabolic effects of MnCl 2 ‐labeling were also assessed using assays for cell viability, proliferation, and apoptosis. Finally, in vivo Mn 2+ ‐guided MRI of the transplanted hESC was successfully achieved and validated by bioluminescence imaging. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.
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