Purpose: this study was conducted on the effects of vitrification cryotop method on gene expression of mature oocytes in Mus musculus.
Methods: transcript analyses of three mouse genes, namely Mater, Hook1 and Sod1, were performed upon non-vitrified and vitrified oocytes with different concentrations of dimethyl sulfoxide (DMSO) and ethylene glycol (EG),15%: 7.5% DMSO + 7.5% EG, and 30%: 15% DMSO + 15% EG, using cryotop following normalization of transcripts with Hprt1 by nested quantitative PCR.
Results: vitrification caused down-regulation of Mater and Hook1 and up-regulation of Sod1 when lower concentrations of cryoprotectants were used as opposed to the control group. The relative expression of Sod1 in vit(2) (30% v/v) was significantly higher than vit(1) (15% v/v)(.) Quantitative transcript analysis of Mater and Hook1 for the vit(2) condition failed to produce any data. Survival rates were the same for both vitrification treatments and significantly lower than control group.
Conclusions: although vit(1) treatment had lower survival rate compared to control group, it demonstrated better stability comparing to vit(2) based on the transcript analysis.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995428 | PMC |
http://dx.doi.org/10.1007/s10815-010-9453-0 | DOI Listing |
Hum Reprod
February 2014
Department of Obstetrics and Gynaecology, Seoul National University Bundang Hospital, 300 Gumi, Bundang, Seongnam, Gyeonggi 463-707 Korea.
Study Question: Does exposure to lysophosphatidic acid (LPA) during in vitro maturation (IVM) enhance the maturation and developmental competence of mouse oocytes?
Summary Answer: Supplementation of IVM medium with 30 μM LPA enhanced the developmental competence of in vitro matured oocytes and so made them more comparable to in vivo matured control oocytes.
What Is Known Already: LPA is a small phospholipid that acts as an extracellular signaling molecule by binding to and activating at least five G protein-coupled receptors. LPA has various biological actions, with both developmental and physiological effects.
J Assist Reprod Genet
November 2010
Cellular and Molecular Biology Research Center, Medical School of Shaheed Beheshti University of Medical Sciences and Health Services, Parvaneh St. Yaman St. Chamran highway, Tehran, Iran.
Purpose: this study was conducted on the effects of vitrification cryotop method on gene expression of mature oocytes in Mus musculus.
Methods: transcript analyses of three mouse genes, namely Mater, Hook1 and Sod1, were performed upon non-vitrified and vitrified oocytes with different concentrations of dimethyl sulfoxide (DMSO) and ethylene glycol (EG),15%: 7.5% DMSO + 7.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!