4.3 Article Proceedings Paper

Recovery of human mesenchymal stem cells following dehydration and rehydration

Journal

CRYOBIOLOGY
Volume 43, Issue 2, Pages 182-187

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1006/cryo.2001.2361

Keywords

human mesenchymal stem cells; dehydration; vacuums; trehalose; glycerol

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A cell therapies advance from research laboratories to clinical application. there is die need to transport cells and tissues across long distances while maintaining cell viability and function. Currently cells are successfull stored and shipped under liquid nitrogen vapor, The ability to store these cells in die desiccated state at ambient temperature would provide tremendous economic and practical ad advantage. Human mesenchymal stem cells (hMSCs) have broad potential uses in tissue engineering and regeneration since they can differentiate along multiple lineages and Support hematopoeisis. The current research applied recent technological advances in the dehydration and storage of human fibroblasts to HMSCs. Three conditions were tested: air-dried. air-dried and stored under vacuum (vacuum only). and incubated with 50 mM trehalose + 3% glycerol and then air-dried and stored under vacuum (vacuum + trehalose). Plates containing dehydrated hMSCs were shipped from San Diego to Baltimore overnight in separate FedEx cardboard boxes. The hMSCs were rehydrated with 3 ml of hMSC medium and were able to regain their spindle-shaped morphology and adhesive capability. In addition, they maintained high liability and proliferation capacity. Rehydrated and passaged cells continued to express the characteristic hMSC surface antigen panel. Additionally, cells showed constitutive levels of mRNA for a stromal factor and. when exposed to reagents known to induce differentiation, demonstrated upregulation of two tissue-specific messages indicative of differentiation potential for fat and bone. While our preliminary findings are encouraging, we still need to address consistency and duration of storage by considering factors such as cell water content. oxygen concentration. and the presence of free radicals. (C) 2001 Elsevier Science (USA).

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