肥胖哮喘患儿CD4+ t淋巴细胞单细胞转录谱的差异

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Vickram Tejwani, Rulin Wang, Andres Villabona-Rueda, Karthik Suresh, Tianshi David Wu, Ian M Adcock, Nazanin Z Kermani, Joe Zein, Nadia N Hansel, Srinivasan Yegnasubramanian, Meredith C McCormack, Franco R D'Alessio
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引用次数: 0

摘要

肥胖是哮喘发病的一个危险因素,与吸入皮质类固醇反应性较差有关。CD4+ t细胞是哮喘免疫学的核心,并可能导致独特的肥胖哮喘表型。我们试图描述肥胖哮喘儿童与正常体重哮喘儿童单细胞CD4+转录谱的差异。方法:对8名体重正常和肥胖的哮喘患者进行临床表型分析,并根据哮喘对照进行匹配。外周血CD4+ t细胞分选,单细胞RNA测序。通过典型基因表达、差异基因表达和反应组通路分析鉴定细胞簇。在我们的队列中也评估了来自U-BIOPRED儿科队列的肥胖PB大量转录组特征。结果:肥胖儿童哮喘具有明显的CD4+转录谱和差异基因表达。肥胖儿童PTPRC高活性细胞较多,PTPRClow活性细胞较少。肥胖儿童中性粒细胞脱粒、白细胞介素-7 (IL-7)受体和IL-7相关janus激酶信号转导和转录信号通路激活因子的富集程度较高。先前与更严重哮喘相关的基因IL-32、FKBP5基因表达、IL-6和Rho转录信号也在肥胖哮喘患儿中富集。讨论:我们的研究结果揭示了肥胖儿童中更严重和类固醇抵抗性哮喘的分子机制。需要进一步的研究来确定这一群体潜在的新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distinct single-cell transcriptional profile in CD4+ T-lymphocytes among obese children with asthma.

Obesity is a risk factor for asthma morbidity, associated with less responsiveness to inhaled corticosteroids. CD4+ T cells are central to the immunology of asthma and may contribute to the unique obese asthma phenotype. We sought to characterize the single-cell CD4+ transcriptional profile differences in obese children with asthma compared with normal-weight children with asthma. Eight normal-weight and obese participants with asthma were clinically phenotyped and matched based on asthma control. Peripheral blood (PB) CD4+ T cells were sorted, and single-cell RNA sequencing was conducted. Cell clusters were identified by canonical gene expression and differential gene expression and reactome pathway analysis was applied. The obese PB bulk transcriptomic signature from the U-BIOPRED pediatric cohort was assessed in our cohort as well. Obese children with asthma have a distinct CD4+ transcriptional profile with differential gene expression. There were more activated protein tyrosine phosphate receptor type C (PTPRC)high cells and less PTPRClow in children with obesity. Children with obesity had higher enrichment of the neutrophil degranulation, interleukin-7 (IL-7) receptor, and IL-7-related janus kinase-signal transducer and activator of transcription signaling pathways. Genes previously associated with more severe asthma, IL-32, FKBP5 gene expression, IL-6, and Rho transcriptional signaling, were also enriched in obese children with asthma. Our findings shed insight into the molecular mechanisms underpinning more severe and steroid-resistant asthma among children with obesity. Further investigation is needed to identify potential new therapeutic targets for this group.NEW & NOTEWORTHY This study identified unique contributors to asthma in children with obesity and found novel pathways. Increased expression of IL-7R, IL-32, PARP-1, FKBP5 gene, IL-6, and Rho transcriptional signaling were observed in obese individuals with asthma.

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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