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Updated: Aug 12, 2025

Characterizing Extracellular Vesicles from Biological Fluids
Published on: February 28, 2025
Developmental trajectory of extracellular vesicle characteristics from the lungs of preterm infants
Meaghan A Ransom1, Kaitlyn E Bunn2, Nicholas M Negretti1
1Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Insights
Extracellular vesicles (EVs) in premature infants change during lung development. EV profiles are linked to bronchopulmonary dysplasia (BPD) risk, offering potential therapeutic targets.
Area of Science:
- Neonatal Research
- Pulmonology
- Cell Biology
Background:
- Extracellular vesicles (EVs) are investigated as biomarkers and therapeutics for lung diseases like bronchopulmonary dysplasia (BPD).
- Limited understanding exists regarding EV content, cargo, and function in premature infant lung development.
Purpose of the Study:
- To characterize EVs during human lung development in premature neonates.
- To investigate the association between EV profiles, gestational age, and BPD risk.
Main Methods:
- Tracheal aspirates from premature neonates (22–35 wk gestational age) were analyzed.
- Techniques included nanoparticle tracking analysis, electron microscopy, and bead-based flow cytometry.
- Murine lung epithelial cell expression data were queried for EV marker changes.
Main Results:
- EVs were detected across lung development stages, with larger sizes observed earlier in gestation.
- EVs contained tetraspanins (CD9, CD63, CD81) and epithelial/immune cell markers.
- Increased EV surface proteins (CD24, CD14) correlated with gestational age and BPD risk.
Conclusions:
- EV profiles are associated with lung development and gestational age in premature infants.
- Specific EV surface markers may predict BPD risk.
- These findings support further research into EVs as therapeutic targets for BPD.
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.
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