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周细胞:被肺部遗忘的细胞类型。

Pericytes: The lung-forgotten cell type.

作者信息

Garrison Annelise T, Bignold Rebecca E, Wu Xinhui, Johnson Jill R

机构信息

School of Biosciences, College of Health and Life Sciences, Aston University, Birmingham, United Kingdom.

Department of Molecular Pharmacology, Faculty of Science and Engineering, University of Groningen, Groningen, Netherlands.

出版信息

Front Physiol. 2023 Mar 23;14:1150028. doi: 10.3389/fphys.2023.1150028. eCollection 2023.

Abstract

Pericytes are a heterogeneous population of mesenchymal cells located on the abluminal surface of microvessels, where they provide structural and biochemical support. Pericytes have been implicated in numerous lung diseases including pulmonary arterial hypertension (PAH) and allergic asthma due to their ability to differentiate into scar-forming myofibroblasts, leading to collagen deposition and matrix remodelling and thus driving tissue fibrosis. Pericyte-extracellular matrix interactions as well as other biochemical cues play crucial roles in these processes. In this review, we give an overview of lung pericytes, the key pro-fibrotic mediators they interact with, and detail recent advances in preclinical studies on how pericytes are disrupted and contribute to lung diseases including PAH, allergic asthma, and chronic obstructive pulmonary disease (COPD). Several recent studies using mouse models of PAH have demonstrated that pericytes contribute to these pathological events; efforts are currently underway to mitigate pericyte dysfunction in PAH by targeting the TGF-β, CXCR7, and CXCR4 signalling pathways. In allergic asthma, the dissociation of pericytes from the endothelium of blood vessels and their migration towards inflamed areas of the airway contribute to the characteristic airway remodelling observed in allergic asthma. Although several factors have been suggested to influence this migration such as TGF-β, IL-4, IL-13, and periostin, recent evidence points to the CXCL12/CXCR4 pathway as a potential therapeutic target. Pericytes might also play an essential role in lung dysfunction in response to ageing, as they are responsive to environmental risk factors such as cigarette smoke and air pollutants, which are the main drivers of COPD. However, there is currently no direct evidence delineating the contribution of pericytes to COPD pathology. Although there is a lack of human clinical data, the recent available evidence derived from and animal-based models shows that pericytes play important roles in the initiation and maintenance of chronic lung diseases and are amenable to pharmacological interventions. Therefore, further studies in this field are required to elucidate if targeting pericytes can treat lung diseases.

摘要

周细胞是位于微血管腔外表面的间充质细胞异质群体,在那里它们提供结构和生化支持。由于周细胞能够分化为形成瘢痕的肌成纤维细胞,导致胶原蛋白沉积和基质重塑,从而推动组织纤维化,因此它们与包括肺动脉高压(PAH)和过敏性哮喘在内的多种肺部疾病有关。周细胞与细胞外基质的相互作用以及其他生化信号在这些过程中起着关键作用。在这篇综述中,我们概述了肺周细胞、它们与之相互作用的关键促纤维化介质,并详细介绍了临床前研究的最新进展,这些研究涉及周细胞如何被破坏以及如何导致包括PAH、过敏性哮喘和慢性阻塞性肺疾病(COPD)在内的肺部疾病。最近几项使用PAH小鼠模型的研究表明,周细胞促成了这些病理事件;目前正在努力通过靶向转化生长因子-β(TGF-β)、CXC趋化因子受体7(CXCR7)和CXC趋化因子受体4(CXCR4)信号通路来减轻PAH中的周细胞功能障碍。在过敏性哮喘中,周细胞从血管内皮解离并向气道炎症区域迁移,促成了过敏性哮喘中观察到的特征性气道重塑。尽管有人提出几种因素会影响这种迁移,如TGF-β、白细胞介素-4(IL-4)、白细胞介素-13(IL-13)和骨膜蛋白,但最近的证据表明CXC趋化因子配体12(CXCL12)/CXCR4通路是一个潜在的治疗靶点。周细胞在衰老引起的肺功能障碍中可能也起着重要作用,因为它们对香烟烟雾和空气污染物等环境风险因素有反应,而这些因素是COPD的主要驱动因素。然而,目前尚无直接证据说明周细胞对COPD病理的贡献。尽管缺乏人类临床数据,但最近从体外和动物模型获得的现有证据表明,周细胞在慢性肺部疾病的发生和维持中起重要作用,并且适合进行药物干预。因此,该领域需要进一步研究以阐明靶向周细胞是否可以治疗肺部疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d704/10076600/afc1774f3e48/fphys-14-1150028-g001.jpg

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