Zhang Xinxin, Shi Xiaoni, Xie Feiyan, Liu Yaping, Wei Xinyan, Cai Yu, Chao Jie
Jiangsu Provincial Key Laboratory of Critical Care Medicine, Zhongda Hospital, Department of Physiology, School of Medicine, Southeast University, Nanjing, Jiangsu, 210009, China.
Department of Histology and Embryology, School of Medicine, Southeast University, Nanjing 210009, PR China.
Heliyon. 2023 Aug 23;9(9):e19428. doi: 10.1016/j.heliyon.2023.e19428. eCollection 2023 Sep.
Lung fibroblasts are the major components in the connective tissue of the pulmonary interstitium and play essential roles in the developing of postnatal lung, synthesizing the extracellular matrix and maintaining the integrity of the lung architecture. Fibroblasts are activated in various disease conditions and exhibit functional heterogeneities according to their origin, spatial location, activated state and microenvironment. In recent years, advances in technology have enabled researchers to identify fibroblast subpopulations in both mouse and human. Here, we discuss pulmonary fibroblast heterogeneity, focusing on the developing, healthy and pathological lung conditions. We firstly review the expression profiles of fibroblasts during lung development, and then consider fibroblast diversity according to different anatomical sites of lung architecture. Subsequently, we discuss fibroblast heterogeneity in genetic lineage. Finally, we focus on how fibroblast heterogeneity may shed light on different pathological lung conditions such as fibrotic diseases, infectious diseases including COVID-19, and lung cancers. We emphasize the importance of comparative studies to illuminate the overlapping characteristics, expression profiles and signaling pathways of the fibroblast subpopulations across disease conditions, a better characterization of the functional complexity rather than the expression of a particular gene may have important therapeutic applications.
肺成纤维细胞是肺间质结缔组织的主要成分,在出生后肺的发育、细胞外基质的合成以及肺结构完整性的维持中发挥着重要作用。成纤维细胞在各种疾病状态下被激活,并根据其起源、空间位置、激活状态和微环境表现出功能异质性。近年来,技术的进步使研究人员能够在小鼠和人类中识别成纤维细胞亚群。在此,我们讨论肺成纤维细胞的异质性,重点关注发育中的、健康的和病理状态下的肺情况。我们首先回顾肺发育过程中成纤维细胞的表达谱,然后根据肺结构的不同解剖部位考虑成纤维细胞的多样性。随后,我们讨论遗传谱系中的成纤维细胞异质性。最后,我们重点关注成纤维细胞异质性如何为不同的病理性肺疾病,如纤维化疾病、包括COVID-19在内的传染病和肺癌,提供线索。我们强调比较研究的重要性,以阐明跨疾病状态的成纤维细胞亚群的重叠特征、表达谱和信号通路,更好地表征功能复杂性而非特定基因的表达可能具有重要的治疗应用价值。