Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Blood. 2012 Mar 15;119(11):2545-51. doi: 10.1182/blood-2011-09-378356. Epub 2012 Jan 23.
In vivo imaging has revolutionized understanding of the spatiotemporal complexity that subserves the generation of successful effector and regulatory immune responses. Until now, invasive surgery has been required for microscopic access to lymph nodes (LNs), making repeated imaging of the same animal impractical and potentially affecting lymphocyte behavior. To allow longitudinal in vivo imaging, we conceived the novel approach of transplanting LNs into the mouse ear pinna. Transplanted LNs maintain the structural and cellular organization of conventional secondary lymphoid organs. They participate in lymphocyte recirculation and exhibit the capacity to receive and respond to local antigenic challenge. The same LN could be repeatedly imaged through time without the requirement for surgical exposure, and the dynamic behavior of the cells within the transplanted LN could be characterized. Crucially, the use of blood vessels as fiducial markers also allowed precise re-registration of the same regions for longitudinal imaging. Thus, we provide the first demonstration of a method for repeated, noninvasive, in vivo imaging of lymphocyte behavior.
在体成像技术极大地推动了人们对于成功产生效应器和调节性免疫应答的时空复杂性的理解。直到现在,还需要进行侵入性手术才能获得对淋巴结(LNs)的显微镜检查,这使得对同一动物进行重复成像变得不切实际,并可能影响淋巴细胞的行为。为了实现长期的在体成像,我们构思了一种将 LNs 移植到小鼠耳郭的新颖方法。移植的 LNs 保持了传统次级淋巴器官的结构和细胞组织。它们参与淋巴细胞再循环,并具有接受和响应局部抗原挑战的能力。同一个 LN 可以在不进行手术暴露的情况下多次进行时间上的成像,并且可以对移植 LN 内的细胞的动态行为进行特征描述。至关重要的是,血管作为基准标记的使用还允许对同一区域进行精确的重新配准,以进行纵向成像。因此,我们首次证明了一种可重复、非侵入性、在体成像的方法,用于研究淋巴细胞的行为。