Tissue engineering studies were done using isolated cells, three-dimen
sional polymer scaffolds, and rotating bioreactors operated under cond
itions of simulated microgravity. In particular, vessel rotation speed
was adjusted such that 10 mm diameter x 2 mm thick cell-polymer const
ructs were cultivated in a state of continuous free-fall. Feasibility
was demonstrated for two different cell types: cartilage and heart. Co
nditions of simulated microgravity promoted the formation of cartilagi
nous constructs consisting of round cells, collagen and glycosaminogly
can (GAG), and cardiac tissue constructs consisting of elongated cells
that contracted spontaneously and synchronously. Potential advantages
of using a simulated microgravity environment for tissue engineering
were demonstrated by comparing the compositions of cartilaginous const
ructs grown under four different in vitro culture conditions: simulate
d microgravity in rotating bioreactors, solid body rotation in rotatin
g bioreactors, turbulent mixing in spinner flasks, and orbital mixing
in petri dishes. Constructs grown in simulated microgravity contained
the highest fractions of total regenerated tissue (as a percent of con
struct dry weight) and of GAG, the component required for cartilage to
withstand compressive force.