Literature DB >> 32216643

Effect of Equilibration Time and Temperature on Murine Spermatogonial Stem Cell Cryopreservation.

Sang-Eun Jung1, Myongzun Kim2, Jin Seop Ahn1, Yong-Hee Kim1, Bang-Jin Kim3, Min-Hyung Yun1, Joong-Hyuck Auh2, Buom-Yong Ryu1.   

Abstract

Cryopreservation of spermatogonial stem cells (SSCs) is essential for preservation of valuable livestock and clinical applications. Although optimal equilibration of cryoprotectants has emerged as a promising approach to improve the cryopreservation efficiency, standard equilibration protocols have not yet been considered in cryopreservation of SSCs. This study aimed to establish a standard equilibration protocol to improve the cryopreservation efficiency of murine germ cells enriched for SSCs. After time- and temperature-dependent equilibration, the germ cells were cryopreserved with 10% dimethyl sulfoxide (DMSO) and 200 mM trehalose. To investigate cryopreservation efficiency at different equilibration conditions, the survival and proliferation rates were assessed after thawing, and then, cytotoxicity and intracellular trehalose quantification were analyzed. Protein (PLZF, GFRα1, VASA, and c-Kit) and gene (Bcl6b, Erm, Dazl, and Sycp1) expression was determined using immunofluorescence and real-time quantitative polymerase chain reaction (RT-qPCR), respectively. The proliferation rate increased significantly following equilibration for 20 minutes at room temperature (RT; 163.7% ± 24.6%) or 4°C (269.0% ± 18.2%). Cytotoxicity was reduced in 10% DMSO with 200 mM trehalose compared with that of 10% DMSO alone. Also, intracellular trehalose was observed after equilibration. The immunofluorescence and RT-qPCR data revealed that the murine germ cells enriched for SSCs retained their self-renewal ability after cryopreservation following equilibration. The most effective protocol was equilibration with 10% DMSO and 200 mM trehalose for 20 minutes at RT or 4°C, which is due to synergistic effects of intracellular and extracellular trehalose. This improved methodology will contribute toward the development of a standardized freezing protocol for murine germ cells enriched for SSCs and thereby expand their application in various fields.

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Keywords:  DMSO toxicity; cryopreservation; equilibration; spermatogonial stem cells; trehalose

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Year:  2020        PMID: 32216643     DOI: 10.1089/bio.2019.0116

Source DB:  PubMed          Journal:  Biopreserv Biobank        ISSN: 1947-5543            Impact factor:   2.300


  2 in total

1.  Sugar-Assisted Cryopreservation of Stem Cell-Laden Gellan Gum-Collagen Interpenetrating Network Hydrogels.

Authors:  Jian Yao Ng; Kee Ying Fremi Tan; Pui Lai Rachel Ee
Journal:  Biomacromolecules       Date:  2022-06-08       Impact factor: 6.978

2.  Rescue and Conservation of Male Adult Alpacas (Vicugna pacos) Based on Spermatogonial Stem Cell Biotechnology Using Atomized Black Maca as a Supplement of Cryopreservation Medium.

Authors:  Martha Valdivia; Zezé Bravo; Jhakelin Reyes; Gustavo F Gonzales
Journal:  Front Vet Sci       Date:  2021-03-17
  2 in total

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