Establishing the role of gravity in plant requires information about how gravity regulates the metabolism of individual cells. Plant cells and tissues in vitro are valuable models for such purpose. Disrupted intercellular relations in such models have allowed to elucidate both the gravity role in non-specialised to gravity plant cells and the correlative relation role of an intact plant organism. The data obtained from non-numerous space and clinostat experiments with plant cells in vitro have demonstrated that their metabolism is sensitive to g-environment. The most experiments have shown a decrease in the biomass production and cell proliferation of spaceflight samples compared with ground controls, although there is study reporting of increased biomass production in an anise suspension culture and D. carota crown gall tissue culture. At the same time, results of experiments with single carrot cells and tomato callus culture demonstrated similarities in differentiation process in microgravity and in ground controls. Noted ultrastructural arrangement in cells, especially mitochondria and plastids, have been related to altered energy load and functions of organelles in microgravity, as well as changes in the lipid peroxidation and the content of malonic dyaldehyde in a haplopappus tissue culture under altered gravity supposed with modification of membrane structural-functional state. This article focuses on growth aspects of the cultured cells in microgravity and under clinostat conditions and considers those aspects that require further analysis.