Chen Qianqian, Hu Chunmei, Lu Wei, Hang Tianxing, Shao Yan, Chen Cheng, Wang Yanli, Li Nan, Jin Linling, Wu Wei, Wang Hong, Zeng Xiaoning, Xie Weiping
Department of Respiratory and Critical Care Medicine, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
Department of Tuberculosis, the Second Hospital of Nanjing, Nanjing, Jiangsu 210029, China.
J Biomed Res. 2022 May 28;36(3):167-180. doi: 10.7555/JBR.36.20220007.
Tuberculosis (TB), is an infectious disease caused by ( ), and presents with high morbidity and mortality. Alveolar macrophages play an important role in TB pathogenesis although there is heterogeneity and functional plasticity. This study aimed to show the characteristics of alveolar macrophages from bronchioalveolar lavage fluid (BALF) in active TB patients. Single-cell RNA sequencing (scRNA-seq) was performed on BALF cells from three patients with active TB and additional scRNA-seq data from three healthy adults were established as controls. Transcriptional profiles were analyzed and compared by differential geneexpression and functional enrichment analysis. We applied pseudo-temporal trajectory analysis to investigate correlations and heterogeneity within alveolar macrophage subclusters. Alveolar macrophages from active TB patients at the single-cell resolution are described. We found that TB patients have higher cellular percentages in five macrophage subclusters. Alveolar macrophage subclusters with increased percentages were involved in inflammatory signaling pathways as well as the basic macrophage functions. The TB-increased alveolar macrophage subclusters might be derived from M1-like polarization state, before switching to an M2-like polarization state with the development of infection. Cell-cell communications of alveolar macrophages also increased and enhanced in active TB patients. Overall, our study demonstrated the characteristics of alveolar macrophages from BALF in active TB patients by using scRNA-seq.
结核病(TB)是一种由( )引起的传染病,发病率和死亡率都很高。肺泡巨噬细胞在结核病发病机制中起着重要作用,尽管存在异质性和功能可塑性。本研究旨在揭示活动性结核病患者支气管肺泡灌洗液(BALF)中肺泡巨噬细胞的特征。对三名活动性结核病患者的BALF细胞进行了单细胞RNA测序(scRNA-seq),并建立了另外三名健康成年人的scRNA-seq数据作为对照。通过差异基因表达和功能富集分析对转录谱进行分析和比较。我们应用拟时间轨迹分析来研究肺泡巨噬细胞亚群内的相关性和异质性。描述了单细胞分辨率下活动性结核病患者的肺泡巨噬细胞。我们发现,结核病患者在五个巨噬细胞亚群中的细胞百分比更高。百分比增加的肺泡巨噬细胞亚群参与炎症信号通路以及基本的巨噬细胞功能。结核病中增加的肺泡巨噬细胞亚群可能源自M1样极化状态,随着感染的发展转变为M2样极化状态之前。活动性结核病患者中肺泡巨噬细胞的细胞间通讯也增加并增强。总体而言,我们的研究通过使用scRNA-seq展示了活动性结核病患者BALF中肺泡巨噬细胞的特征。