## Abstract Mesenchymal stem cells (MSC) offer great promise in therapies aimed at repairing, replacing or regenerating damaged or diseased tissues and organs. This potential is due to their capacity for selfβrenewal, ability to differentiate down a range of lineages, and potential in autologous th
Design of bioreactors for mesenchymal stem cell tissue engineering
β Scribed by Pankaj Godara; Clive D McFarland; Robert E Nordon
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2008
- Tongue
- English
- Weight
- 290 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0268-2575
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
There is a growing need for efficient mesenchymal stem cell (MSC) production processes for a wide spectrum of clinical conditions ranging from the treatment of lifeβthreatening graftβversusβhost disease to cartilage repair. Development of cell and tissue engineered products derived from MSCs will be enabled by scalable production processes with standards of safety and efficacy similar to those established for the pharmaceutical industry. Many of the bioreactor design principles established for production of biopharmaceuticals can be applied to production of MSC products; however, specific control of the microenvironment is required for MSC expansion and differentiation. We review how porous scaffolds and bioreactor technologies are applied to the study of the MSC microenvironment. Current methods for MSC production are based on growth in tissue culture flasks, which is labourβintensive and expensive. We suggest that stirred, perfusion or microfluidic bioreactor technologies can more efficiently address the clinical need for largeβscale MSC production. Soft lithography and microfluidic design offer extreme geometric precision to study MSC function as well as defining the microenvironment for tissue engineering at the micron scale. Copyright Β© 2008 Society of Chemical Industry
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## Abstract Adult mesenchymal stem cells (MSCs) can be isolated from bone marrow or marrow aspirates and because they are cultureβdish adherent, they can be expanded in culture while maintaining their multipotency. The MSCs have been used in preclinical models for tissue engineering of bone, cartil