Cell Cycle Arrest in G 2 /M Promotes Early Steps of Infection by Human Immunodeficiency Virus

Abstract

ABSTRACT We have identified four small molecules that boost transduction of cells by human immunodeficiency virus (HIV) and investigated their mechanism of action. These molecules include etoposide and camptothecin, which induce DNA damage by inhibiting religation of cleaved topoisomerase-DNA complexes, taxol, which interferes with the function of microtubules, and aphidicolin, which inhibits DNA polymerases. All four compounds arrest the cell cycle at G 2 /M, though in addition high concentrations of aphidicolin arrest in G 1 . We find that early events of HIV replication, including synthesis of late reverse transcription products, two-long terminal repeat circles, and integrated proviruses, were increased after treatment of cells with concentrations of each compound that arrested in G 2 /M. Stimulation was seen for both transformed cell lines (293T and HeLa cells) and primary cells (IMR90 lung fibroblasts). Arrest in G 1 with high concentrations of aphidicolin boosted transduction, though not much as with lower concentrations that arrested in G 2 /M. Arrest of IMR90 cells in G 1 by serum starvation and contact inhibition reduced transduction. Previously, the proteasome inhibitor MG132 was reported to increase HIV infection—here we investigated the effects of combinations of the cell cycle inhibitors with MG132 and obtained data suggesting that MG132 may also boost transduction by causing G 2 /M cell cycle arrest. These data document that cell cycle arrest in G 2 /M boosts the early steps of HIV infection and suggests methods for increasing transduction with HIV-based vectors.