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Updated: May 23, 2026

Harnessing the Power of MicroRNA Cargoes in Small Extracellular Vesicles Released from Fresh-Frozen Human Brain Sections
Published on: November 8, 2024
Microvesicles: novel biomarkers for neurological disorders
Elisa Colombo1, Bruno Borgiani, Claudia Verderio
1Clinical Neuroimmunology Unit, Division of Neuroscience, Institute of Experimental Neurology, San Raffaele Scientific Institute Milan, Italy.
Abstract:
Microvesicles (MVs) are released by most cell types in physiological conditions, but their number is often increased upon cellular activation or neoplastic transformation. This suggests that their detection may be helpful in pathological conditions to have information on activated cell types and, possibly, on the nature of the activation. This could be of paramount importance in districts and tissues that are not accessible to direct examination, such as the central nervous system. Increased release of MVs has been described to be associated to the acute or active phase of several neurological disorders. While the subcellular origin of MVs (exosome or ectosomes) is basically never addressed in these studies because of technical limitations, the cell of origin is always identified. Endothelium- or platelet-derived MVs, detected in plasma or serum, are linked to neurological pathologies with a vascular or ischemic pathogenic component, and may represent a very useful marker to support therapeutic choices in stroke. In neuroinflammatory disorders, such as multiple sclerosis, MVs of oligodendroglial, or microglial origin have been described in the cerebrospinal fluid and may carry, in perspective, additional information on the biological alterations in their cell of origin. Little specific evidence is available in neurodegenerative disorders and, specifically, MVs of neural origin have never been investigated in these pathologies. Few data have been reported for neuroinfection and brain trauma. In brain tumors, despite the limited number of studies performed, results are very promising and potentially close to clinical translation. We here review all currently available data on the detection of MVs in neurological diseases, limiting our search to exclusively human studies. Current literature and our own data indicate that MVs detection may represent a very promising strategy to gain pathogenic information, identify therapeutic targets, and select specific biomarkers for neurological disorders.
Insights
Detecting microvesicles (MVs) in neurological diseases offers promising insights into disease mechanisms and potential biomarkers. Increased MV levels signal cellular activation, aiding diagnosis and therapeutic choices in conditions like stroke and neuroinflammation.
Area of Science:
- Neuroscience
- Cell Biology
- Biomarker Discovery
Background:
- Microvesicles (MVs) are released by cells and increase during activation or neoplastic transformation.
- Increased MV release is linked to acute phases of several neurological disorders.
- MV detection offers potential insights into activated cell types and disease pathology, especially in inaccessible tissues like the CNS.
Purpose of the Study:
- To review current human studies on microvesicle detection in neurological diseases.
- To explore the potential of MVs as diagnostic and prognostic biomarkers.
- To identify therapeutic targets based on MV analysis.
Main Methods:
- Systematic review of human studies focusing on microvesicle detection in neurological disorders.
- Analysis of MV origin (endothelial, platelet, oligodendroglial, microglial, neural) and their association with specific diseases.
- Evaluation of the clinical relevance and potential applications of MV detection.
Main Results:
- Endothelial/platelet MVs correlate with vascular/ischemic pathologies (e.g., stroke), supporting therapeutic decisions.
- Oligodendroglial/microglial MVs are found in neuroinflammatory disorders (e.g., multiple sclerosis), potentially indicating cellular alterations.
- Promising, though limited, data exists for brain tumors, suggesting clinical translation potential. Data for neurodegenerative diseases, neuroinfections, and brain trauma are scarce.
Conclusions:
- Microvesicle detection is a promising strategy for gaining pathogenic information in neurological disorders.
- MVs can serve as valuable biomarkers for diagnosis, prognosis, and therapeutic target identification.
- Further investigation, particularly into MVs of neural origin, is warranted across various neurological conditions.

