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Tubuloreticular structures in human lymphoid cell lines. A cell biological study
British Journal of Experimental Pathology
|April 1, 1975
Summary
Bromodeoxyuridine (BrUdR) can induce tubuloreticular structures (TRS) in human lymphoid cells by incorporating into DNA. This induction is independent of ongoing DNA synthesis after incorporation, suggesting a link to latent virus activation.
Area of Science:
- Cell Biology
- Virology
- Molecular Biology
Background:
- Tubuloreticular structures (TRS) are microvilli-like structures found in various cell types.
- Their spontaneous or induced occurrence in human lymphoid cell lines is not fully understood.
- Previous studies suggested a potential link between TRS and Epstein-Barr virus (EBV) associated antigens.
Purpose of the Study:
- To investigate the induction of tubuloreticular structures (TRS) in human lymphoid cell lines.
- To explore the role of bromodeoxyuridine (BrUdR) in TRS formation.
- To determine if TRS are correlated with Epstein-Barr virus (EBV) associated antigens.
Main Methods:
- Culturing EB-3 human lymphoid cell line with bromodeoxyuridine (BrUdR).
- Investigating the effect of thymidine and deoxycytidine on BrUdR-induced TRS.
- Assessing the necessity of BrUdR incorporation time and ongoing DNA synthesis for TRS production.
- Examining spontaneous TRS presence in cell lines lacking EBV antigens.
Main Results:
- Bromodeoxyuridine (BrUdR) successfully induced TRS in EB-3 cells after 96 hours of culture.
- BrUdR-induced TRS formation was blocked by thymidine but not deoxycytidine.
- BrUdR incorporation into DNA for at least 48 hours was necessary for TRS induction.
- TRS were spontaneously present in IHTC-33 cells, which do not produce EBV antigens, excluding a correlation.
Conclusions:
- Bromodeoxyuridine (BrUdR) can induce tubuloreticular structures (TRS) in human lymphoid cells.
- TRS induction by BrUdR is dependent on its incorporation into DNA, not ongoing DNA synthesis.
- The findings exclude a correlation between TRS and Epstein-Barr virus (EBV) associated antigens.
- BrUdR-induced TRS may be linked to the activation of other latent viruses.