Related Experiment Video
Updated: Aug 15, 2026

Flow Virometry to Analyze Antigenic Spectra of Virions and Extracellular Vesicles
Published on: January 25, 2017
Microvesicles and vesicles of multivesicular bodies versus "virus-like" particles
Abstract:
Pellets obtained by the centrifugation of unfiltered or filtered fetal bovine serum (FBS) contained, among other things, numerous elongate and spherical microvesicles, ranging from 30 to 60 nm. They possessed a trilaminar (unit membrane) envelope and a moderately electron-dense core. Vesicles of multivesicular bodies and microvesicles associated with secretory epithelial cells and human lymphoblastoid cells in suspension culture possessed the same structure and were in the same size range as the serum microvesicles. These structures were either normal cell components or they represented the breakdown products of normal cell components and should not be confused with viruses. Though microvesicles of FBS may have been involved in the tissue culture material, at least some of the microvesicles associated with, and phagocytosed by, human lymphoblastoid cells in suspension and those in the lumen of acini of the baboon prostate were derived from the breakdown of the cristae of mitochondria in degenerating cells.
Insights
Microvesicles found in fetal bovine serum (FBS) share structural similarities with cellular vesicles. These serum microvesicles are normal cell components, not viruses, and can originate from mitochondrial breakdown.
Area of Science:
- Cell Biology
- Biochemistry
- Microscopy
Background:
- Fetal bovine serum (FBS) is widely used in cell culture.
- The nature and origin of microvesicles within FBS are not fully understood.
- Distinguishing cellular microvesicles from viral particles is crucial in biological research.
Purpose of the Study:
- To characterize the morphology and origin of microvesicles in fetal bovine serum (FBS).
- To determine if FBS microvesicles are distinct from cellular vesicles.
- To clarify the potential role of FBS microvesicles in cell culture and biological processes.
Main Methods:
- Centrifugation of filtered and unfiltered FBS to isolate microvesicles.
- Transmission electron microscopy (TEM) to analyze vesicle structure and size.
- Comparison of FBS microvesicle morphology with vesicles from cell cultures and biological tissues.
Main Results:
- Pellets from FBS centrifugation contained numerous elongate and spherical microvesicles (30-60 nm).
- These microvesicles exhibited a trilaminar envelope and electron-dense core, similar to cellular vesicles.
- Identical structures were observed in vesicles from multivesicular bodies, secretory epithelial cells, and human lymphoblastoid cells.
- Some microvesicles associated with human lymphoblastoid cells and baboon prostate were traced to the breakdown of mitochondrial cristae.
Conclusions:
- Microvesicles in FBS are structurally consistent with normal cellular components or breakdown products.
- These serum microvesicles should not be mistaken for viruses.
- Mitochondrial degeneration is a source of some microvesicles found in biological samples and potentially in cell culture.
Related Concept Videos
Viral Structure
Intralumenal Vesicles and Multivesicular Bodies
COP Coated Vesicles
Introduction to Virus
Subviral Agents
Human Virome

