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Updated: Nov 15, 2025

An Innovative Method for Exosome Quantification and Size Measurement
Published on: January 17, 2015
Qualitative and Quantitative Comparison of Plasma Exosomes from Neonates and Adults
Julia Peñas-Martínez1, María N Barrachina2, Ernesto José Cuenca-Zamora1
1Servicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Arrixaca, 30003 Murcia, Spain.
Insights
Neonatal plasma exosomes are smaller and contain less protein than adult exosomes, with distinct protein profiles affecting platelet function. This discovery highlights potential risks in transfusions involving plasma exosomes.
Area of Science:
- Biochemistry
- Cell Biology
- Hematology
Background:
- Exosomes mediate intercellular communication, crucial in health and disease.
- Platelet-derived exosomes are abundant in blood.
- Neonatal platelets exhibit hyporeactivity linked to Soluble N-ethylmaleimide-sensitive fusion Attachment protein REceptor (SNARE) protein defects.
Purpose of the Study:
- To investigate differences in plasma-derived exosomes between neonates and adults.
- To explore the impact of age on exosome biogenesis and content.
Main Methods:
- Isolation of plasma-derived exosomes via ultracentrifugation from umbilical cord blood (neonates) and peripheral blood (adults).
- Characterization using transmission electron microscopy for size determination.
- Quantitative proteomic analysis to identify protein content differences.
Main Results:
- Neonatal plasma exosomes were significantly smaller and contained 65% less protein than adult exosomes.
- 131 proteins were differentially expressed: 83 overexpressed and 48 underexpressed in neonatal exosomes.
- Upregulated proteins in neonatal exosomes relate to platelet activation and coagulation; underexpressed proteins include immunoglobulins.
Conclusions:
- This is the first study demonstrating age-dependent changes in exosome size and protein composition.
- Findings suggest a potential "developmental hemostatic mismatch risk" in transfusions involving adult plasma exosomes into neonates.
Abstract:
Exosomes are extracellular vesicles that contain nucleic acids, lipids and metabolites, and play a critical role in health and disease as mediators of intercellular communication. The majority of extracellular vesicles in the blood are platelet-derived. Compared to adults, neonatal platelets are hyporeactive and show impaired granule release, associated with defects in Soluble N-ethylmaleimide-sensitive fusion Attachment protein REceptor (SNARE) proteins. Since these proteins participate in biogenesis of exosomes, we investigated the potential differences between newborn and adult plasma-derived exosomes. Plasma-derived exosomes were isolated by ultracentrifugation of umbilical cord blood from full-term neonates or peripheral blood from adults. Exosome characterization included size determination by transmission electron microscopy and quantitative proteomic analysis. Plasma-derived exosomes from neonates were significantly smaller and contained 65% less protein than those from adults. Remarkably, 131 proteins were found to be differentially expressed, 83 overexpressed and 48 underexpressed in neonatal (vs. adult) exosomes. Whereas the upregulated proteins in plasma exosomes from neonates are associated with platelet activation, coagulation and granule secretion, most of the underexpressed proteins are immunoglobulins. This is the first study showing that exosome size and content change with age. Our findings may contribute to elucidating the potential "developmental hemostatic mismatch risk" associated with transfusions containing plasma exosomes from adults.
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