Article ID Journal Published Year Pages File Type
4982916 Colloids and Surfaces B: Biointerfaces 2017 16 Pages PDF
Abstract

•Lack of scalability of 2-D culture systems.•Physiologically relevant human cell culture techniques.•Techniques mimicking native microenvironment for SC growth and differentiation.•Higher density and billion fold expansion using 3-D culture systems.•Challenges and advantages of 3-D culture systems.

Stem cells (SCs) hold great promise for cell therapy, tissue engineering, and regenerative medicine as well as pharmaceutical and biotechnological applications. They have the capacity to self-renew and the ability to differentiate into specialized cell types depending upon their source of isolation. However, use of SCs for clinical applications requires a high quality and quantity of cells. This necessitates large-scale expansion of SCs followed by efficient and homogeneous differentiation into functional derivatives. Traditional methods for maintenance and expansion of cells rely on two-dimensional (2-D) culturing techniques using plastic culture plates and xenogenic media. These methods provide limited expansion and cells tend to lose clonal and differentiation capacity upon long-term passaging. Recently, new approaches for the expansion of SCs have emphasized three-dimensional (3-D) cell growth to mimic the in vivo environment. This review provides a comprehensive compendium of recent advancements in culturing SCs using 2-D and 3-D techniques involving spheroids, biomaterials, and bioreactors. In addition, potential challenges to achieve billion-fold expansion of cells are discussed.

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Related Topics
Physical Sciences and Engineering Chemical Engineering Colloid and Surface Chemistry
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