Cited by 26Extracellular vesicles in diseaseNeuroinflammation and Neurodegeneration MechanismsMultiple Sclerosis Research Studies

Myeloid extracellular vesicles: messengers from the demented brain

Open access
Nigro, Annamaria, Colombo, Federico, Casella, Giacomo, Finardi, Annamaria, Verderio, Claudia, Furlan, Roberto·2016·Frontiers in Immunology

Abstract

Blood-borne monocyte derived cells play a pivotal, initially unrecognized, role in most central nervous system disorders, including diseases initially classified as purely neurodegenerative (i.e., Alzheimer's disease, Parkinson's disease, and ALS). Their trafficking to the brain and spinal cord has been extensively studied in classical neuroinflammatory disorders such as multiple sclerosis. Central nervous system resident myeloid cells, namely microglia and perivascular macrophages, also are in the spotlight of investigations on neurological disorders. Myeloid cells, such as infiltrating macrophages and microglia, have been described as having both protective and destructive features in neurological disorders, thus identification of their functional phenotype during disease evolution would be of paramount importance. Extracellular vesicles, namely exosomes and shed vesicles, are released by virtually any cell type and can be detected and identified in terms of cell origin in biological fluids. They therefore constitute an ideal tool to access information on cells residing in an inaccessible site such as the brain. We will review here available information on extracellular vesicles detection in neurological disorders with special emphasis on neurodegenerative diseases.

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Crossref · 10.3389/fimmu.2016.00017

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  • Microglial EVs represent a "liquid biopsy" of their parental cells, and could provide information on the functional phenotype (protective or damaging) of microglial cells over the course of neurodegeneration.

    “The microglial EVs representing a “liquid biopsy” of their parental cells, and could provide information on the functional phenotype (protective or damaging) of microglial cells over the course of neurodegeneration (Nigro et al., 2016).”

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Authors
Nigro, A., Colombo, F., Casella, G., Finardi, A., Verderio, C., & Furlan, R.
Affiliations
  • IRCCS Ospedale San Raffaele (IT)
  • National Research Council (IT)
Corresponding author
Furlan, Roberto
Venue
Frontiers in Immunology
Published
2016-01-29
Volume
7
Pages
17-17
ISSN
1664-3224 (ISSN-L)
OpenAlex
W2291996739
Cited by
26
References
40
Citations by year
2024: 2 · 2023: 1 · 2022: 2 · 2021: 4 · 2020: 2 · 2019: 2 · 2018: 7 · 2017: 3 · 2016: 3
FWCI
0.45
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Frontiers in Immunology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
Funders
  • Fondazione Italiana Sclerosi Multipla (2014/R/9)
  • Ministero dell’Istruzione, dell’Università e della Ricerca (Cluster Alisei - Ivascomar)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
exosomes, neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, microglia, perivascular macrophages, monocyte-derived cells, blood-brain barrier, neuroinflammation

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