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Published on: August 9, 2019
Thymic dendritic cells are primary targets for the oncogenic virus SL3-3
C H Uittenbogaart1, W Law, P J Leenen
1Departments of Pediatrics, UCLA School of Medicine, Los Angeles, California, USA. uit-tenbo@ucla.edu
Journal of Virology
|November 13, 1998
Summary
Murine retrovirus SL3-3 initially infects thymic dendritic cells after neonatal inoculation. Macrophages become infected later, followed by spread to thymocytes, leading to malignant lymphoma.
Area of Science:
- Virology
- Immunology
- Oncology
Background:
- Murine retrovirus SL3-3 induces thymic lymphoma in mice.
- Understanding the initial cellular targets is crucial for elucidating lymphomagenesis.
Purpose of the Study:
- Identify the primary target cells of SL3-3 virus in the thymus following neonatal inoculation.
- Trace the early cellular tropism and spread of the virus within the thymus.
Main Methods:
- Immunohistochemistry to detect viral envelope glycoprotein (gp70) expression.
- Cell separation techniques to isolate infected cell populations.
- Infectious cell center assays to quantify infectious virus spread.
Main Results:
- gp70(+) cells, identified as dendritic cells, were first observed in the thymus cortex and corticomedullary junction at 2 weeks post-inoculation.
- Macrophages also expressed gp70 starting at 3 weeks, co-localizing with dendritic cells.
- Virus expression was not initially detected in epithelial or lymphoid cells; infectious virus spread to thymocytes occurred later.
Conclusions:
- Thymic dendritic cells are the initial primary target cells for SL3-3 retrovirus infection after neonatal inoculation.
- Subsequent infection of macrophages and eventual spread to thymocytes facilitate provirus integration and clonal lymphoma development.
- This sequential infection pathway highlights the critical role of specific thymic stromal cells in retroviral lymphomagenesis.
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