Document Type : Original Article
Department of Cell and Molecular Biology, Faculty of Biology, College of Science, University of Tehran, Tehran, Iran
Department of Embryology, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
Department of Genetics, Reproductive Biomedicine Research Centre, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
Department of Biochemistry, Faculty of Basic Sciences and Advanced Technologies in Biology, University of Science and Culture, Tehran, Iran
Objective: Choosing the optimal method for human sperm cryopreservation seems necessary to reduce cryoinjury.
The aim of this study is to compare two cryopreservation methods including rapid-freezing and vitrification, in terms
of cellular parameters, epigenetic patterns and expression of paternally imprinted genes (PAX8, PEG3 and RTL1) in
human sperm which play a role in male fertility.
Materials and Methods: In this experimental study, semen samples were collected from 20 normozoospermic men.
After washing the sperms, cellular parameters were investigated. DNA methylation and expression of genes were
investigated using methylation-specific polymerase chain reaction (PCR) and real-time PCR methods, respectively.
Results: The results showed a significant decrease in sperm motility and viability, while a significant increase was
observed in DNA fragmentation index of cryopreserved groups in comparison with the fresh group. Moreover, a significant
reduction in sperm total motility (TM, P<0.01) and viability (P<0.01) was determined, whereas a significant increase
was observed in DNA fragmentation index (P<0.05) of the vitrification group compared to the rapid-freezing group.
Our results also showed a significant decrease in expression of PAX8, PEG3 and RTL1 genes in the cryopreserved
groups compared to the fresh group. However, expression of PEG3 (P<0.01) and RTL1 (P<0.05) genes were reduced
in the vitrification compared to the rapid-freezing group. Moreover, a significant increase in the percentage of PAX8,
PEG3 and RTL1 methylation was detected in the rapid-freezing group (P<0.01, P<0.0001 and P<0.001, respectively)
and vitrification group (P<0.01, P<0.0001 and P<0.0001, respectively) compared to the fresh group. Additionally,
percentage of PEG3 and RTL1 methylation in the vitrification group was significantly increased (P<0.05 and P<0.05,
respectively) compared to the rapid-freezing group.
Conclusion: Our findings showed that rapid-freezing is more suitable method for maintaining sperm cell quality. In
addition, due to the role of these genes in fertility, changes in their expression and epigenetic modification may affect