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Updated: Aug 17, 2026

Purification of High Yield Extracellular Vesicle Preparations Away from Virus
Published on: September 12, 2019
Endosomes, exosomes and Trojan viruses
Annegret Pelchen-Matthews1, Graça Raposo, Mark Marsh
1Cell Biology Unit, MRC Laboratory for Molecular Cell Biology and Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT, UK. a.pelchen-matthews@ucl.ac.uk
Abstract:
Retroviruses are enveloped viruses that are generally assumed to bud at the plasma membrane of infected cells. Recently it has become apparent that some of these viruses use the endocytic pathway to coordinate their assembly and release. In addition, these and some other enveloped viruses exploit the machinery that generates the internal membranes of multivesicular bodies (MVB). These observations and others have led to the suggestion that retroviruses be regarded as "viral exosomes". Here we discuss this concept and the emerging evidence that compartments of the endocytic pathway play important roles in the biogenesis of both the internal vesicles of MVB and viruses.
Insights
Retroviruses, enveloped viruses, may bud from internal cell compartments, not just the plasma membrane. This suggests viral exosomes, utilizing endocytic pathways for assembly and release.
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- Retroviruses are typically thought to bud from the plasma membrane.
- Emerging evidence suggests alternative viral assembly and release mechanisms.
Purpose of the Study:
- To discuss the concept of retroviruses as "viral exosomes".
- To review evidence for the endocytic pathway's role in viral biogenesis.
Main Methods:
- Literature review and conceptual discussion.
Main Results:
- Some enveloped viruses, including retroviruses, utilize the endocytic pathway for assembly and release.
- Viruses exploit multivesicular body (MVB) biogenesis machinery.
Conclusions:
- Retroviruses may be considered "viral exosomes".
- Endocytic pathway compartments are crucial for MVB and viral particle formation.
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