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Published on: July 6, 2013
The minute virus of mice exploits different endocytic pathways for cellular uptake
Pierre O Garcin1, Nelly Panté1
1Department of Zoology, University of British Columbia, Vancouver, British Columbia, Canada.
Abstract:
The minute virus of mice, prototype strain (MVMp), is a non-enveloped, single-stranded DNA virus of the family Parvoviridae. Unlike other parvoviruses, the mechanism of cellular uptake of MVMp has not been studied in detail. We analyzed MVMp endocytosis in mouse LA9 fibroblasts and a tumor cell line derived from epithelial-mesenchymal transition through polyomavirus middle T antigen transformation in transgenic mice. By a combination of immunofluorescence and electron microscopy, we found that MVMp endocytosis occurs at the leading edge of migrating cells in proximity to focal adhesion sites. By using drug inhibitors of various endocytic pathways together with immunofluorescence microscopy and flow cytometry analysis, we discovered that MVMp can use a number of endocytic pathways, depending on the host cell type. At least three different mechanisms were identified: clathrin-, caveolin-, and clathrin-independent carrier-mediated endocytosis, with the latter occurring in transformed cells but not in LA9 fibroblasts.
Insights
Minute virus of mice (MVMp) cellular uptake was investigated. MVMp utilizes distinct endocytic pathways, including clathrin- and caveolin-mediated, depending on the host cell type.
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- The Minute virus of mice (MVMp), a parvovirus, lacks detailed cellular uptake mechanism studies.
- Understanding viral entry is crucial for comprehending viral pathogenesis and developing interventions.
Purpose of the Study:
- To elucidate the cellular uptake mechanisms of MVMp in different host cell types.
- To investigate the role of endocytic pathways in MVMp entry.
Main Methods:
- Immunofluorescence microscopy and electron microscopy were employed to visualize MVMp endocytosis.
- Drug inhibitors targeting specific endocytic pathways were used in conjunction with flow cytometry.
- MVMp entry was analyzed in mouse LA9 fibroblasts and a transformed epithelial-mesenchymal transition cell line.
Main Results:
- MVMp endocytosis was observed at the leading edge of migrating cells near focal adhesions.
- MVMp utilized clathrin-mediated endocytosis in LA9 fibroblasts.
- Transformed cells employed clathrin-, caveolin-, and clathrin-independent carrier-mediated endocytosis for MVMp entry.
Conclusions:
- MVMp employs diverse endocytic strategies for cellular entry, varying with host cell context.
- The identified pathways offer insights into parvovirus-host cell interactions.
- Cellular transformation influences the endocytic mechanisms utilized by MVMp.
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