Umashankar Abhishek, Corenblum Mandi J, Ray Sneha, Valdez Michel, Yoshimaru Eriko S, Trouard Theodore P, Madhavan Lalitha
Department of Neurology, University of Arizona, Tucson, AZ, USA; Neuroscience and Cognitive Science Undergraduate Program, Undergraduate Biology Research Program, University of Arizona, Tucson, AZ, USA.
Department of Neurology, University of Arizona, Tucson, AZ, USA.
Int J Nanomedicine. 2016 Apr 27;11:1731-48. doi: 10.2147/IJN.S102006. eCollection 2016.
An essential component of developing successful neural stem cell (NSC)-based therapies involves the establishment of methodologies to noninvasively monitor grafted NSCs within brain tissues in real time. In this context, ex vivo labeling with ultrasmall superparamagnetic iron oxide (USPIO) particles has been shown to enable efficient tracking of transplanted NSCs via magnetic resonance imaging (MRI). However, whether and how USPIO labeling affects the intrinsic biology of NSCs is not thoroughly understood, and remains an active area of investigation. Here, we perform a comprehensive examination of rat NSC survival and regenerative function upon labeling with the USPIO, Molday ION Rhodamine B (MIRB), which allows for dual magnetic resonance and optical imaging. After optimization of labeling efficiency, two specific doses of MIRB (20 and 50 μg/mL) were chosen and were followed for the rest of the study. We observed that both MIRB doses supported the robust detection of NSCs, over an extended period of time in vitro and in vivo after transplantation into the striata of host rats, using MRI and post hoc fluorescence imaging. Both in culture and after neural transplantation, the higher 50 μg/mL MIRB dose significantly reduced the survival, proliferation, and differentiation rate of the NSCs. Interestingly, although the lower 20 μg/mL MIRB labeling did not produce overtly negative effects, it increased the proliferation and glial differentiation of the NSCs. Additionally, application of this dose also changed the morphological characteristics of neurons and glia produced after NSC differentiation. Importantly, the transplantation of NSCs labeled with either of the two MIRB doses upregulated the immune response in recipient animals. In particular, in animals receiving the 50 μg/mL MIRB-labeled NSCs, this immune response consisted of an increased number of CD68(+)-activated microglia, which appeared to have phagocytosed MIRB particles and cells contributing to an exaggerated MRI signal dropout in the animals. Overall, these results indicate that although USPIO particles, such as MIRB, may have advantageous labeling and magnetic resonance-sensitive features for NSC tracking, a further examination of their effects might be necessary before they can be used in clinical scenarios of cell-based transplantation.
开发成功的基于神经干细胞(NSC)疗法的一个关键组成部分是建立能够实时无创监测移植到脑组织中的NSC的方法。在这种情况下,用超小超顺磁性氧化铁(USPIO)颗粒进行体外标记已被证明能够通过磁共振成像(MRI)有效追踪移植的NSC。然而,USPIO标记是否以及如何影响NSC的内在生物学特性尚未得到充分了解,仍是一个活跃的研究领域。在此,我们对用USPIO、莫尔戴离子罗丹明B(MIRB)标记的大鼠NSC的存活和再生功能进行了全面检查,MIRB可实现双磁共振和光学成像。在优化标记效率后,选择了两种特定剂量的MIRB(20和50μg/mL),并在研究的其余部分持续跟踪。我们观察到,使用MRI和事后荧光成像,两种MIRB剂量都能在体外长时间以及在移植到宿主大鼠纹状体后的体内有力地检测到NSC。在培养和神经移植后,较高的50μg/mL MIRB剂量显著降低了NSC的存活、增殖和分化率。有趣的是,尽管较低的20μg/mL MIRB标记没有产生明显的负面影响,但它增加了NSC的增殖和胶质细胞分化。此外,应用该剂量还改变了NSC分化后产生的神经元和胶质细胞的形态特征。重要的是,用两种MIRB剂量之一标记的NSC移植上调了受体动物的免疫反应。特别是,在接受50μg/mL MIRB标记的NSC的动物中,这种免疫反应表现为CD68(+)激活的小胶质细胞数量增加,这些小胶质细胞似乎吞噬了MIRB颗粒和细胞,导致动物体内MRI信号丢失加剧。总体而言,这些结果表明,尽管USPIO颗粒(如MIRB)可能对NSC追踪具有有利的标记和磁共振敏感特性,但在将其用于基于细胞的移植临床方案之前,可能有必要进一步研究它们的影响。