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与食蟹猴肺部健康衰老相关的功能、转录和微生物变化。

Functional, transcriptional, and microbial shifts associated with healthy pulmonary aging in rhesus macaques.

机构信息

Department of Molecular Biology and Biochemistry, University of California Irvine, Irvine, CA, USA.

Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR, USA.

出版信息

Cell Rep. 2022 Apr 19;39(3):110725. doi: 10.1016/j.celrep.2022.110725.

Abstract

Older individuals are at increased risk of developing severe respiratory infections. However, our understanding of the impact of aging on the respiratory tract remains limited as samples from healthy humans are challenging to obtain and results can be confounded by variables such as smoking and diet. Here, we carry out a comprehensive cross-sectional study (n = 34 adult, n = 49 aged) to define the consequences of aging on the lung using the rhesus macaque model. Pulmonary function testing establishes similar age and sex differences as humans. Additionally, we report increased abundance of alveolar and infiltrating macrophages and a concomitant decrease in T cells were in aged animals. scRNAseq reveals shifts from GRZMB to IFN expressing CD8 T cells in the lungs. These data provide insight into age-related changes in the lungs' functional, microbial, and immunological landscape that explain increased prevalence and severity of respiratory diseases in the elderly.

摘要

老年人患严重呼吸道感染的风险增加。然而,由于难以从健康人群中获得样本,并且结果可能受到吸烟和饮食等变量的干扰,因此我们对衰老对呼吸道的影响的了解仍然有限。在这里,我们使用恒河猴模型进行了一项全面的横断面研究(n=34 名成年人,n=49 名老年人),以定义衰老对肺部的影响。肺功能测试确立了与人类相似的年龄和性别差异。此外,我们报告说,老年动物的肺泡和浸润巨噬细胞数量增加,而 T 细胞相应减少。scRNAseq 显示肺部中 GRZMB 表达的 CD8 T 细胞向 IFN 表达的 CD8 T 细胞转变。这些数据提供了对与年龄相关的肺部功能、微生物和免疫学特征变化的深入了解,这些变化解释了老年人中呼吸道疾病的发病率和严重程度增加的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aa6/9096119/0dfe159e928f/nihms-1801593-f0002.jpg

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