Department of Microbiology, Immunology and Cancer Biology, University of Virginia, Charlottesville, USA; Carter Immunology Center, University of Virginia, Charlottesville, USA.
Carter Immunology Center, University of Virginia, Charlottesville, USA; Department of Chemistry, University of Virginia, Charlottesville, USA.
J Immunol Methods. 2021 Feb;489:112943. doi: 10.1016/j.jim.2020.112943. Epub 2020 Dec 14.
Lymph nodes (LNs) are essential secondary immune organs where the adaptive immune response is generated against most infections and vaccines. We recently described the use of live ex vivo LN slices to study the dynamics of adaptive immunity. However, when working with reactive lymph nodes from vaccinated animals, the tissues frequently became dislodged from the supportive agarose matrix during slicing, leading to damage that prevented downstream analysis. Because reactive lymph nodes expand into the surrounding adipose tissue, we hypothesized that dislodging was a result of excess lipids on the collagen capsule of the LN, and that a brief wash with a mild detergent would improve LN interaction with the agarose without damaging tissue viability or function. Therefore, we tested the use of digitonin on improving slicing of vaccinated LNs. Prior to embedding, LNs were quickly dipped into a digitonin solution and washed in saline. Lipid droplets were visibly removed by this procedure. A digitonin wash step prior to slicing significantly reduced the loss of LN during slicing from 13 to 75% to 0-25%, without substantial impact on viability. Capture of fluorescent microparticles, uptake and processing of protein antigen, and cytokine secretion in response to a vaccine adjuvant, R848, were all unaffected by the detergent wash. This novel approach will enable ex vivo analysis of the generation of adaptive immune response in LNs in response to vaccinations and other immunotherapies.
淋巴结 (LNs) 是生成适应性免疫反应的主要次级免疫器官,大多数感染和疫苗都会引发适应性免疫反应。我们最近描述了使用活体 LN 切片来研究适应性免疫反应的动态。然而,在处理来自接种疫苗动物的反应性淋巴结时,组织在切片过程中经常从琼脂糖基质上脱落,导致组织受损,无法进行下游分析。由于反应性淋巴结会扩散到周围的脂肪组织中,我们假设脱落是由于 LN 胶原囊上的多余脂质引起的,并且用温和的去污剂进行短暂洗涤可以改善 LN 与琼脂糖的相互作用,而不会损害组织活力或功能。因此,我们测试了使用胆钙化醇来改善接种 LN 的切片。在包埋之前,LN 迅速浸入胆钙化醇溶液中,并用生理盐水洗涤。通过该程序可以明显去除脂质滴。在切片之前进行胆钙化醇洗涤步骤可将 LN 在切片过程中的损失从 13% 降低至 75%至 0%至 25%,而对活力的影响不大。荧光微球的捕获、蛋白质抗原的摄取和加工以及对疫苗佐剂 R848 的细胞因子分泌均不受去污剂洗涤的影响。这种新方法将能够对外来疫苗和其他免疫疗法引发的 LN 适应性免疫反应的生成进行体外分析。