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早产儿肺部细胞外囊泡特征的发育轨迹。

Developmental trajectory of extracellular vesicle characteristics from the lungs of preterm infants.

机构信息

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2023 Mar 1;324(3):L385-L392. doi: 10.1152/ajplung.00389.2022. Epub 2023 Jan 31.

Abstract

Extracellular vesicles (EVs) are secreted lipid-enclosed particles that have emerged as potential biomarkers and therapeutic agents in lung disease, including bronchopulmonary dysplasia (BPD), a leading complication of preterm birth. Many unanswered questions remain about the content and cargo of EVs in premature infants and their role in lung development. To characterize EVs during human lung development, tracheal aspirates were collected from premature neonates between 22 and 35 wk gestational age and analyzed via nanoparticle tracking analysis, electron microscopy, and bead-based flow cytometry. EVs were detectable across late canalicular through saccular stages of lung development, demonstrating larger sizes earlier in gestation. EVs contained an abundance of the EV-enriched tetraspanins CD9, CD63, and CD81, as well as epithelial cell and immune cell markers. Increases in select surface proteins (CD24 and CD14) on EVs were associated with gestational age and with the risk of BPD. Finally, query of expression data obtained from epithelial cells in a single-cell atlas of murine lung development found that epithelial EV marker expression also changes with developmental time. Together, these data demonstrate an association between EV profile and lung development and provide a foundation for future functional classification of EVs, with the goal of determining their role in cell signaling during development and harnessing their potential as a new therapeutic target in BPD.

摘要

细胞外囊泡 (EVs) 是分泌的脂质包裹颗粒,已成为肺部疾病(包括支气管肺发育不良 (BPD))的潜在生物标志物和治疗剂,BPD 是早产儿的主要并发症。关于早产儿 EVs 的内容和货物及其在肺发育中的作用,仍有许多悬而未决的问题。为了在人类肺发育过程中对 EVs 进行特征描述,我们从胎龄 22 至 35 周的早产儿的气管吸出物中收集标本,并通过纳米颗粒跟踪分析、电子显微镜和基于珠子的流式细胞术进行分析。在肺发育的晚期小管腔到囊泡阶段都可检测到 EVs,这表明 EVs 在妊娠早期体积较大。EVs 中含有丰富的 EV 富集四跨膜蛋白 CD9、CD63 和 CD81,以及上皮细胞和免疫细胞标志物。EVs 上某些表面蛋白(CD24 和 CD14)的增加与胎龄和 BPD 风险相关。最后,对从单个细胞图谱中获得的小鼠肺发育过程中上皮细胞的表达数据进行查询,发现上皮细胞 EV 标志物的表达也随发育时间而变化。总之,这些数据表明 EV 特征与肺发育之间存在关联,并为 EV 的未来功能分类提供了基础,目标是确定它们在发育过程中的细胞信号传递中的作用,并利用它们作为 BPD 的新治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f6b/10026990/0b7ebe735e87/l-00389-2022r01.jpg

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