Sellers Stephanie L, Payne Geoffrey W
Interdisciplinary Science, University of Northern British Columbia.
J Vis Exp. 2011 Apr 4(50):2551. doi: 10.3791/2551.
Lymph nodes (LN's), located throughout the body, are an integral component of the immune system. They serve as a site for induction of adaptive immune response and therefore, the development of effector cells. As such, LNs are key to fighting invading pathogens and maintaining health. The choice of LN to study is dictated by accessibility and the desired model; the inguinal lymph node is well situated and easily supports studies of biologically relevant models of skin and genital mucosal infection. The inguinal LN, like all LNs, has an extensive microvascular network supplying it with blood. In general, this microvascular network includes the main feed arteriole of the LN that subsequently branches and feeds high endothelial venules (HEVs). HEVs are specialized for facilitating the trafficking of immune cells into the LN during both homeostasis and infection. How HEVs regulate trafficking into the LN under both of these circumstances is an area of intense exploration. The LN feed arteriole, has direct upstream influence on the HEVs and is the main supply of nutrients and cell rich blood into the LN. Furthermore, changes in the feed arteriole are implicated in facilitating induction of adaptive immune response. The LN microvasculature has obvious importance in maintaining an optimal blood supply to the LN and regulating immune cell influx into the LN, which are crucial elements in proper LN function and subsequently immune response. The ability to study the LN microvasculature in vivo is key to elucidating how the immune system and the microvasculature interact and influence one another within the LN. Here, we present a method for in vivo imaging of the inguinal lymph node. We focus on imaging of the microvasculature of the LN, paying particular attention to methods that ensure the study of healthy vessels, the ability to maintain imaging of viable vessels over a number of hours, and quantification of vessel magnitude. Methods for perfusion of the microvasculature with vasoactive drugs as well as the potential to trace and quantify cellular traffic are also presented. Intravital microscopy of the inguinal LN allows direct evaluation of microvascular functionality and real-time interface of the direct interface between immune cells, the LN, and the microcirculation. This technique potential to be combined with many immunological techniques and fluorescent cell labelling as well as manipulated to study vasculature of other LNs.
淋巴结(LN)遍布全身,是免疫系统不可或缺的组成部分。它们是诱导适应性免疫反应以及效应细胞发育的场所。因此,淋巴结是对抗入侵病原体和维持健康的关键。选择研究的淋巴结取决于其可及性和所需模型;腹股沟淋巴结位置便利,能很好地支持对皮肤和生殖器黏膜感染的生物学相关模型的研究。与所有淋巴结一样,腹股沟淋巴结有广泛的微血管网络为其供血。一般来说,这个微血管网络包括淋巴结的主要供血小动脉,该小动脉随后分支并为高内皮微静脉(HEV)供血。高内皮微静脉专门用于在稳态和感染期间促进免疫细胞进入淋巴结。在这两种情况下,高内皮微静脉如何调节进入淋巴结的细胞运输是一个深入探索的领域。淋巴结供血小动脉对高内皮微静脉有直接的上游影响,是营养物质和富含细胞的血液进入淋巴结的主要供应途径。此外,供血小动脉的变化与促进适应性免疫反应的诱导有关。淋巴结微血管系统对于维持向淋巴结的最佳血液供应以及调节免疫细胞流入淋巴结具有明显的重要性,而这是淋巴结正常功能以及随后免疫反应的关键要素。在体内研究淋巴结微血管系统的能力是阐明免疫系统和微血管系统在淋巴结内如何相互作用和相互影响的关键。在此,我们介绍一种腹股沟淋巴结体内成像方法。我们专注于淋巴结微血管系统的成像,特别关注确保对健康血管进行研究、在数小时内维持对存活血管成像的能力以及血管大小量化的方法。还介绍了用血管活性药物灌注微血管系统的方法以及追踪和量化细胞运输的潜力。腹股沟淋巴结活体显微镜检查可以直接评估微血管功能以及免疫细胞、淋巴结和微循环之间直接界面的实时情况。这项技术有可能与许多免疫学技术和荧光细胞标记相结合,并可用于研究其他淋巴结的血管系统。