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Neural stem cells (NSCs) are of great value for clinical application and scientific research. The development of efficient cryopreservation protocols could significantly facilitate the storage and transportation for clinic applications. The objective of the present study is to improve the survival rate and viability of NSCs. Neural stem cells with three states of single-cell suspension, NSC spheres with diameters of 30-50 microm and 80-100 microm, were cryopreserved by slow-freezing method with the cryoprotective agent (CPA) of dimethyl sulfoxide (Me(2)SO), respectively. Then the post-thawing NSCs were tested for the survival rate and the differentiation ability. As a result, NSC spheres with diameter of 80-100 microm and Me(2)SO concentration of 8% achieve the survival rate of 82.9%, and the NSCs still sustain the multi-differentiation potentiality. These results indicated that both the subtle interaction among NSCs and sphere diameters may affect the survival rate together.

Original publication

DOI

10.1016/j.cryobiol.2009.10.013

Type

Journal article

Journal

Cryobiology

Publication Date

04/2010

Volume

60

Pages

184 - 191

Keywords

Animals, Benzimidazoles, Cell Culture Techniques, Cell Differentiation, Cell Size, Cell Survival, Cryopreservation, Cryoprotective Agents, Dimethyl Sulfoxide, Embryonic Stem Cells, Fluorescent Dyes, Neurons, Propidium, Rats, Time Factors