Use of microgravity bioreactors for development of an in vitro rat salivary gland cell culture model

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Abstract
During development, salivary gland (SG) cells both secrete factors which modulate cellular behavior and express specific hormone receptors. Whether SG cell growth is modulated by an autocrine epidermal growth factor (EGF) receptor‐mediated signal transduction pathway is not clearly understood. SG tissue is the synthesis site for functionally distinct products including growth factors, digestive enzymes, and homeostasis maintaining factors. Historically, SG cells have proven difficult to grow and may be only maintained as limited three‐dimensional ductal‐type structures in collagen gels or on reconstituted basement membrane gels. A novel approach to establishing primary rat SG cultures is use of microgravity bioreactors originally designed by NASA as low‐shear culture systems for predicting cell growth and differentiation in the microgravity environment of space. These completely fluid‐filled bioreactors, which are oriented horizontally and rotate, have proven advantageous for Earth‐based culture of three‐dimensional cell assemblies, tissue‐like aggregates, and glandular structures. Use of microgravity bioreactors for establishing in vitro models to investigate steroid‐mediated secretion of EGF by normal SG cells may also prove useful for the investigation of cancer and other salivary gland disorders. These microgravity bioreactors promise challenging opportunities for future applications in basic and applied cell research.