“Our research raises the intriguing possibility that widely used cholesterol-lowering drugs might have an effect in humans similar to what we have found in these initial laboratory studies,” says Eric O. Freed, Ph.D., an investigator in NIAID’s Laboratory of Molecular Microbiology, and the senior author of a paper published in the November 20 issue of Proceedings of the National Academy of Sciences.
HIV, like everything else passing into or out of an animal cell, must navigate the cell’s complex double-walled outer membrane. Much like a bog, a cell membrane contains some areas of relatively solid material while other regions are more fluid. Among the features of this constantly shifting landscape are small, cholesterol-rich patches called rafts, which are more solid than the surrounding membrane and are able to move about like a raft on water.
Rafts are believed to be most concentrated at points of cell-to-cell contact in the immune cells that HIV targets for infection. Any mechanism that helps HIV find and attach to rafts would help the virus spread. Conversely, even a modest degree of disruption could slow the virus’ spread because it would hinder the virus’ ability to enter and leave its host cells.
Scientists have known for some time that an HIV protein called Gag must attach to the inner surface of the cell membrane before new viruses can be produced. Scientists also suspected that Gag’s attachment to the membrane is not random, but rather targets specific regions of the cell surface. The new research shows their suspicions were correct.
Dr. Freed and his co-author Akira Ono, Ph.D., first established that Gag does indeed attach to rafts. They then created several mutant forms of Gag and learned that two pieces of the protein are required for successful attachment. Finally, the investigators turned to the key question of what happens when HIV is kept off the rafts.
To determine this, they depleted cholesterol from rafts using two compounds, one of which removes cholesterol rapidly from the cell surface and one that inhibits cholesterol synthesis. When used alone, each compound significantly reduced HIV’s ability to form particles that could infect new cells. Applied simultaneously to virus-producing cells, the compounds almost completely abolished HIV’s power to replicate.
“Our findings are clear evidence that Gag-raft association is a critical step in HIV replication,” says Dr. Freed. “Additional experiments are needed to determine whether this interaction can be interrupted therapeutically to treat HIV-infected people.”
Reference: A Ono and EO Freed. Plasma membrane rafts play a critical role in HIV-1 assembly and release. Proceedings of the National Academy of Sciences 98:13925-13930 (2001). DOI: 10.1073/pnas.241320298.
Copies of the research paper are available from the PNAS news office at (202) 334-2138 or by e-mail from pnasnews@nas.edu.
Press releases, fact sheets and other NIAID-related materials are available on the NIAID Web site at http://www.niaid.nih.gov.
Journal
Proceedings of the National Academy of Sciences