Simulated microgravity within the NASA High Aspect Rotating-Wall Vessel (HARV) provides a quiescent environment to culture fragile insect cells. In this vessel, the duration of stationary and death phase for cultures of Spodoptera frugiperda cells was greatly extended over that achieved in shaker-flask controls. For both HARV and control cultures, S. frugiperda cells grew to concentrations in excess of 1 × 10 7 viable cell ml −1 with viabilities greater than 90%. In the HARV, stationary phase was maintained 9–15 days in contrast to 4–5 days in the shaker flask. Furthermore, the rate of cell death was reduced in the HARV by a factor of 20–90 relative to the control culture and was characterized with a death rate constant of 0.01–0.02 day −1. Beginning in the stationary phase and continuing in the death phase, there was a significant decrease in population size in the HARV versus an increase in the shaker flask. This phenomenon could represent cell adaptation to simulated microgravity and/or a change in the ratio of apoptotic to necrotic cells. Differences observed in this research between the HARV and its control were attributed to a reduction in hydrodynamic forces in the microgravity vessel.