Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment: Effect of cryopreservation procedures

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Oleksandr Gryshkov
  • Nicola Hofmann
  • Lothar Lauterboeck
  • Denys Pogozhykh
  • Thomas Mueller
  • Birgit Glasmacher

Research Organisations

External Research Organisations

  • Hannover Medical School (MHH)
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Details

Original languageEnglish
Pages (from-to)103-111
Number of pages9
JournalCRYOBIOLOGY
Volume71
Issue number1
Early online date14 May 2015
Publication statusPublished - 1 Aug 2015

Abstract

Multipotent stromal cells derived from the common marmoset monkey Callithrix jacchus (cjMSCs) possess high phylogenetic similarity to humans, with a great potential for preclinical studies in the field of regenerative medicine. Safe and effective long-term storage of cells is of great significance to clinical and research applications. Encapsulation of such cell types within alginate beads that can mimic an extra-cellular matrix and provide a supportive environment for cells during cryopreservation, has several advantages over freezing of cells in suspension. In this study we have analysed the effect of dimethyl sulfoxide (Me2SO, 2.5-10%, v/v) and pre-freeze loading time of alginate encapsulated cjMSCs in Me2SO (0-45. min) on the viability and metabolic activity of the cells after freezing using a slow cooling rate (-1. °C/min). It was found that these parameters affect the stability and homogeneity of alginate beads after thawing. Moreover, the cjMSCs can be frozen in alginate beads with lower Me2SO concentration of 7.5% after 30. min of loading, while retaining high cryopreservation outcome. We demonstrated the maximum viability, membrane integrity and metabolic activity of the cells under optimized, less cytotoxic conditions. The results of this study are another step forward towards the application of cryopreservation for the long-term storage and subsequent applications of transplants in cell-based therapies.

Keywords

    Alginate bead, Common marmoset, Cryopreservation, Dimethyl sulfoxide, Encapsulation, High voltage, Ice formation, Multipotent stromal cells, Stem cells, Viability

ASJC Scopus subject areas

Cite this

Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment: Effect of cryopreservation procedures. / Gryshkov, Oleksandr; Hofmann, Nicola; Lauterboeck, Lothar et al.
In: CRYOBIOLOGY, Vol. 71, No. 1, 01.08.2015, p. 103-111.

Research output: Contribution to journalArticleResearchpeer review

Gryshkov O, Hofmann N, Lauterboeck L, Pogozhykh D, Mueller T, Glasmacher B. Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment: Effect of cryopreservation procedures. CRYOBIOLOGY. 2015 Aug 1;71(1):103-111. Epub 2015 May 14. doi: 10.1016/j.cryobiol.2015.05.001
Gryshkov, Oleksandr ; Hofmann, Nicola ; Lauterboeck, Lothar et al. / Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment : Effect of cryopreservation procedures. In: CRYOBIOLOGY. 2015 ; Vol. 71, No. 1. pp. 103-111.
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title = "Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment: Effect of cryopreservation procedures",
abstract = "Multipotent stromal cells derived from the common marmoset monkey Callithrix jacchus (cjMSCs) possess high phylogenetic similarity to humans, with a great potential for preclinical studies in the field of regenerative medicine. Safe and effective long-term storage of cells is of great significance to clinical and research applications. Encapsulation of such cell types within alginate beads that can mimic an extra-cellular matrix and provide a supportive environment for cells during cryopreservation, has several advantages over freezing of cells in suspension. In this study we have analysed the effect of dimethyl sulfoxide (Me2SO, 2.5-10%, v/v) and pre-freeze loading time of alginate encapsulated cjMSCs in Me2SO (0-45. min) on the viability and metabolic activity of the cells after freezing using a slow cooling rate (-1. °C/min). It was found that these parameters affect the stability and homogeneity of alginate beads after thawing. Moreover, the cjMSCs can be frozen in alginate beads with lower Me2SO concentration of 7.5% after 30. min of loading, while retaining high cryopreservation outcome. We demonstrated the maximum viability, membrane integrity and metabolic activity of the cells under optimized, less cytotoxic conditions. The results of this study are another step forward towards the application of cryopreservation for the long-term storage and subsequent applications of transplants in cell-based therapies.",
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T1 - Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment

T2 - Effect of cryopreservation procedures

AU - Gryshkov, Oleksandr

AU - Hofmann, Nicola

AU - Lauterboeck, Lothar

AU - Pogozhykh, Denys

AU - Mueller, Thomas

AU - Glasmacher, Birgit

N1 - Funding Information: Statement of funding: This study was in part supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation, EXC 62/1). Funding Information: This research was in part supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation, EXC 62/1) through a scholarship by the Cluster of Excellence REBIRTH. The authors thank Julia Struss, Debapriya Saha and Anamika Chatterjee for technical assistance and Prof. S. Schlatt for the kind donation of placental material.

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N2 - Multipotent stromal cells derived from the common marmoset monkey Callithrix jacchus (cjMSCs) possess high phylogenetic similarity to humans, with a great potential for preclinical studies in the field of regenerative medicine. Safe and effective long-term storage of cells is of great significance to clinical and research applications. Encapsulation of such cell types within alginate beads that can mimic an extra-cellular matrix and provide a supportive environment for cells during cryopreservation, has several advantages over freezing of cells in suspension. In this study we have analysed the effect of dimethyl sulfoxide (Me2SO, 2.5-10%, v/v) and pre-freeze loading time of alginate encapsulated cjMSCs in Me2SO (0-45. min) on the viability and metabolic activity of the cells after freezing using a slow cooling rate (-1. °C/min). It was found that these parameters affect the stability and homogeneity of alginate beads after thawing. Moreover, the cjMSCs can be frozen in alginate beads with lower Me2SO concentration of 7.5% after 30. min of loading, while retaining high cryopreservation outcome. We demonstrated the maximum viability, membrane integrity and metabolic activity of the cells under optimized, less cytotoxic conditions. The results of this study are another step forward towards the application of cryopreservation for the long-term storage and subsequent applications of transplants in cell-based therapies.

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