Institut für Anatomie, Zentrum für medizinische Struktur- und Zellbiologie, Universität zu Lübeck, Lübeck, Germany.
PLoS One. 2013;8(2):e55201. doi: 10.1371/journal.pone.0055201. Epub 2013 Feb 8.
Lymphatic vessels play a pivotal role in fluid drainage and egress of immune cells from the lung. However, examining murine lung lymphatics is hampered by the expression of classical lymph endothelial markers on other cell types, which hinders the unambiguous identification of lymphatics. The expression of CD90/Thy-1 on lymph endothelium was recently described and we therefore examined its suitability to identify murine pulmonary lymph vessels under healthy and inflammatory conditions.
METHODOLOGY/PRINCIPAL FINDINGS: Immunohistochemistry with a monoclonal antibody against CD90.2/Thy-1.2 on 200 µm thick precision cut lung slices labeled a vascular network that was distinct from blood vessels. Preembedding immunostaining and electron microscopy verified that the anti-CD90.2/Thy-1.2 antibody labeled lymphatic endothelium. Absence of staining in CD90.1/Thy-1.1 expressing FVB mice indicated that CD90/Thy-1 was expressed on lymph endothelium and labeling was not due to antibody cross reactivity. Double-labeling immunohistochemistry for CD90/Thy-1 and α-smooth muscle actin identified two routes for lymph vessel exit from the murine lung. One started in the parenchyma or around veins and left via venous blood vessels. The other began in the space around airways or in the space between airways and pulmonary arteries and left via the main bronchi. As expected from the pulmonary distribution of lymph vessels, intranasal application of house dust mite led to accumulation of T cells around veins and in the connective tissue between airways and pulmonary arteries. Surprisingly, increased numbers of T cells were also detected around intraacinar arteries that lack lymph vessels. This arterial T cell sheath extended to the pulmonary arteries where lymph vessels were located.
CONCLUSIONS/SIGNIFICANCE: These results indicate that CD90/Thy-1 is expressed on lymphatic endothelial cells and represents a suitable marker for murine lung lymph vessels. Combining CD90/Thy-1 labeling with precision cut lung slices allows visualizing the anatomy of the lymphatic system in normal and inflamed conditions.
淋巴管在肺内液体引流和免疫细胞的输出中起着关键作用。然而,由于经典的淋巴管内皮标志物在其他细胞类型上的表达,使得检查小鼠肺淋巴管受到阻碍,从而无法明确识别淋巴管。最近描述了 CD90/Thy-1 在淋巴管内皮上的表达,因此我们研究了其在健康和炎症条件下识别小鼠肺淋巴管的适用性。
方法/主要发现:使用针对 CD90.2/Thy-1.2 的单克隆抗体对 200µm 厚的精密切割肺切片进行免疫组织化学染色,标记出一种与血管不同的血管网络。预包埋免疫染色和电子显微镜验证了抗 CD90.2/Thy-1.2 抗体标记淋巴管内皮。在表达 CD90.1/Thy-1.1 的 FVB 小鼠中不存在染色表明 CD90/Thy-1 表达于淋巴管内皮,并且标记不是由于抗体的交叉反应性。CD90/Thy-1 和 α-平滑肌肌动蛋白的双标记免疫组织化学鉴定了从小鼠肺中淋巴管逸出的两种途径。一种始于实质或静脉周围,通过静脉血管离开。另一种始于气道周围或气道与肺动脉之间的空间,并通过主支气管离开。与淋巴管在肺部的分布一致,经鼻腔给予屋尘螨导致 T 细胞在静脉周围和气道与肺动脉之间的结缔组织中积聚。令人惊讶的是,在缺乏淋巴管的腺泡内动脉周围也检测到更多的 T 细胞。这个动脉 T 细胞鞘延伸到位于淋巴管的肺动脉。
结论/意义:这些结果表明 CD90/Thy-1 表达于淋巴管内皮细胞,是小鼠肺淋巴管的合适标志物。将 CD90/Thy-1 标记与精密切割肺切片结合使用,可以在正常和炎症条件下可视化淋巴管系统的解剖结构。