Influence of cryopreservation on the CATSPER2 and TEKT2 expression levels and protein levels in human spermatozoa

•The cryopreservation process could lead to a reduction in the expression levels of the CATSPER2 and TEKT2 gene in human spermatozoa.•The cryopreservation process could lead to a down-regulation in the expression of CATSPER2 and TEKT2 gene in human spermatozoa.•The cryopreservation process could lea...

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Veröffentlicht in:Toxicology reports 2019-01, Vol.6, p.819-824
Hauptverfasser: Alshawa, Eiman, Laqqan, Mohammed, Montenarh, Mathias, Hammadeh, Mohamad Eid
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Sprache:eng
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Zusammenfassung:•The cryopreservation process could lead to a reduction in the expression levels of the CATSPER2 and TEKT2 gene in human spermatozoa.•The cryopreservation process could lead to a down-regulation in the expression of CATSPER2 and TEKT2 gene in human spermatozoa.•The cryopreservation process could lead to a reduction in the level of CatSper 2 and Tektin 2 protein in human spermatozoa.•The CatSper 2 and Tektin 2 may be used as markers to explain the causes of motility loss in the spermatozoa after the cryopreservation process. This study designed to assess the expression level of CATSPER2 and TEKT2 and to evaluate the levels of CatSper2 and Tektin2 proteins in human spermatozoa before and after cryopreservation. One hundred and twenty semen samples were included in this study. All the samples were subjected to qPCR and Western blot analysis. The results showed a significant reduction in the expression levels of CATSPER2 and TEKT2 in the cryopreserved compared to the fresh samples (P = 0.0039 and P = 0.0166, respectively), and the results showed down-regulation in the expression level of CATSPER2 and TEKT2 genes between the study groups. Moreover, the protein levels of the CatSper2 and Tektin2 were lower in cryopreserved samples compared to fresh samples (P = 0.0001). In conclusion, the reduction in the proteins level and expression level of the CATSPER2 and TEKT2 in cryopreserved samples could be used as an indicator of sperm motility loss.
ISSN:2214-7500
2214-7500
DOI:10.1016/j.toxrep.2019.08.004