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Updated: Aug 8, 2026

Imaging of HIV-1 Envelope-induced Virological Synapse and Signaling on Synthetic Lipid Bilayers
Published on: March 8, 2012
Budding process and maturation of human immunodeficiency virus examined by means of pre- and post-embedding
T Katsumoto1, M Asanaka, S Kageyama
1Department of Virology, Tottori University School of Medicine, Yonago, Japan.
Insights
Pre- and post-embedding immunogold electron microscopy effectively revealed human immunodeficiency virus (HIV) morphogenesis. These techniques are valuable for studying viral development and antigen localization during HIV replication.
Area of Science:
- Virology
- Cell Biology
- Microscopy
Background:
- Persistent infection of U-937 cells with human immunodeficiency virus (HIV) strain LAV provides a model for studying viral morphogenesis.
- Understanding the intricate process of viral assembly and release is crucial for developing effective antiviral strategies.
Purpose of the Study:
- To evaluate the utility of pre- and post-embedding immunogold electron microscopy techniques for analyzing HIV morphogenesis.
- To characterize the specific stages and locations of HIV replication within infected U-937 cells.
Main Methods:
- Utilized pre- and post-embedding immunogold electron microscopy on U-937/LAV cells.
- Examined viral budding, antigen distribution, and virion morphology.
Main Results:
- HIV budding was localized to membrane regions near the Golgi apparatus.
- Viral envelope antigens were concentrated on electron-dense crescent structures at the cell surface.
- Released virions exhibited either doughnut-shaped or conical cores, with p24 proteins localized to these cores.
Conclusions:
- Pre- and post-embedding immunogold electron microscopy are highly effective for studying viral morphogenesis.
- These techniques provide detailed insights into the structural organization and replication dynamics of HIV.
Abstract:
The techniques of pre- and post-embedding immunocolloidal gold electron microscopy were tested for their usefulness for analyzing the morphogenesis of human immunodeficiency virus (HIV) strain LAV employing U-937 cells persistently infected with the virus (U-937/LAV). By both techniques the following results were obtained. (1) Budding process was restricted to a localized area at the membrane adjacent to the Golgi apparatus. (2) The distribution of viral envelope antigens was restricted to the electron-dense crescent structures on the cell surface. (3) Virions released from the cells could be classified mainly into 2 categories: virions with doughnut-shaped cores or with conical cores at the center of the particles. And p24 proteins localized on the thick electron-dense cores of both types. These findings support the idea that pre- and post-embedding immunogold electron microscopy is very useful for studying the morphogenesis of viruses.
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