Matheu Melanie P, Parker Ian, Cahalan Michael D
Department of Physiology and Biophysics, University of California, Irvine, CA, USA.
J Vis Exp. 2007(7):265. doi: 10.3791/265. Epub 2007 Aug 23.
Two-photon imaging has revealed an elegant choreography of motility and cellular interactions within the lymph node under basal conditions and at the initiation of an immune response (1). Here, we present methods for adoptive transfer of labeled T cells, isolation of lymph nodes, and imaging motility of CD4+ T cells in the explanted lymph node as first described in 2002 (2). Two-photon imaging of immune cells requires that the cells are fluorescently labeled, either by staining with a cell tracker dye or by expressing a fluorescent protein. We demonstrate the adoptive transfer procedure of injecting cells derived from donor mice into the tail vein of a recipient animal, where they home to lymphoid organs within approximately 15-30 min. We illustrate the isolation of a lymph node and describe methods to ensure proper mounting of the excised lymph node. Other considerations such as proper oxygenation of perfused media, temperature, and laser power are discussed. Finally, we present 3D video images of naive CD4+ T cells exhibiting steady state motility at 37 degrees C.
双光子成像揭示了在基础条件下以及免疫反应启动时淋巴结内细胞运动和细胞间相互作用的精妙编排(1)。在此,我们介绍标记T细胞的过继转移、淋巴结的分离以及2002年首次描述的(2)体外培养淋巴结中CD4+ T细胞运动成像的方法。免疫细胞的双光子成像要求细胞通过细胞追踪染料染色或表达荧光蛋白进行荧光标记。我们展示了将供体小鼠来源的细胞注射到受体动物尾静脉的过继转移程序,细胞在大约15 - 30分钟内归巢至淋巴器官。我们说明了淋巴结的分离方法,并描述了确保正确固定切除淋巴结的方法。还讨论了其他注意事项,如灌注培养基的适当氧合、温度和激光功率。最后,我们展示了在37摄氏度下呈现稳态运动的初始CD4+ T细胞的3D视频图像。