Baharom Faezzah, Rankin Gregory, Scholz Saskia, Pourazar Jamshid, Ahlm Clas, Blomberg Anders, Smed-Sörensen Anna
Immunology and Allergy Unit, Department of Medicine Solna, Karolinska Institutet.
Division of Medicine, Department of Public Health and Clinical Medicine, Umeå University.
J Vis Exp. 2017 Jan 20(119):55222. doi: 10.3791/55222.
The lungs are constantly exposed to the external environment, which in addition to harmless particles, also contains pathogens, allergens, and toxins. In order to maintain tolerance or to induce an immune response, the immune system must appropriately handle inhaled antigens. Lung dendritic cells (DCs) are essential in maintaining a delicate balance to initiate immunity when required without causing collateral damage to the lungs due to an exaggerated inflammatory response. While there is a detailed understanding of the phenotype and function of immune cells such as DCs in human blood, the knowledge of these cells in less accessible tissues, such as the lungs, is much more limited, since studies of human lung tissue samples, especially from healthy individuals, are scarce. This work presents a strategy to generate detailed spatial and phenotypic characterization of lung tissue resident DCs in healthy humans that undergo a bronchoscopy for the sampling of endobronchial biopsies. Several small biopsies can be collected from each individual and can be subsequently embedded for ultrafine sectioning or enzymatically digested for advanced flow cytometric analysis. The outlined protocols have been optimized to yield maximum information from small tissue samples that, under steady-state conditions, contain only a low frequency of DCs. While the present work focuses on DCs, the methods described can directly be expanded to include other (immune) cells of interest found in mucosal lung tissue. Furthermore, the protocols are also directly applicable to samples obtained from patients suffering from pulmonary diseases where bronchoscopy is part of establishing the diagnosis, such as chronic obstructive pulmonary disease (COPD), sarcoidosis, or lung cancer.
肺脏持续暴露于外部环境中,该环境除了含有无害颗粒外,还包含病原体、过敏原和毒素。为了维持耐受性或诱导免疫反应,免疫系统必须妥善处理吸入的抗原。肺树突状细胞(DCs)对于维持微妙的平衡至关重要,以便在需要时启动免疫反应,同时不会因过度的炎症反应而对肺脏造成附带损害。虽然人们对人类血液中DCs等免疫细胞的表型和功能有详细的了解,但对于肺等较难获取组织中的这些细胞的认识则更为有限,因为对人类肺组织样本,尤其是来自健康个体的样本的研究很少。这项工作提出了一种策略,用于对健康人类肺组织驻留DCs进行详细的空间和表型特征分析,这些个体因接受支气管镜检查以获取支气管内活检样本。可以从每个个体收集多个小活检样本,随后可将其包埋用于超薄切片,或进行酶消化以用于先进的流式细胞术分析。所概述的方案已进行优化,以便从小组织样本中获取最大信息,这些样本在稳态条件下仅含有低频的DCs。虽然目前的工作重点是DCs,但所描述的方法可以直接扩展到包括在肺黏膜组织中发现的其他感兴趣的(免疫)细胞。此外,这些方案也直接适用于从患有肺部疾病的患者获得的样本,在这些疾病中支气管镜检查是确立诊断的一部分,如慢性阻塞性肺疾病(COPD)、结节病或肺癌。