Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4982916 | Colloids and Surfaces B: Biointerfaces | 2017 | 16 Pages |
â¢Lack of scalability of 2-D culture systems.â¢Physiologically relevant human cell culture techniques.â¢Techniques mimicking native microenvironment for SC growth and differentiation.â¢Higher density and billion fold expansion using 3-D culture systems.â¢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.
Graphical abstractDownload high-res image (75KB)Download full-size image