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Title:Effects of slow freezing and vitrification of human semen on post-thaw semen quality and miRNA expression
Authors:ID Podgrajšek, Rebeka (Author)
ID Bolha, Luka (Author)
ID Pungert, Tjaša (Author)
ID Pižem, Jože (Author)
ID Jazbec Gradišar, Katerina (Author)
ID Maličev, Elvira (Author)
ID Štimpfel, Martin (Author)
Files:.pdf PDF - Presentation file, download (1,73 MB)
MD5: 022FB9FEB5D4336B73887CCBF23A432B
 
URL URL - Source URL, visit https://www.mdpi.com/1422-0067/25/8/4157
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Semen cryopreservation has played an important role in medically assisted reproduction for decades. In addition to preserving male fertility, it is sometimes used for overcoming logistical issues. Despite its proven clinical usability and safety, there is a lack of knowledge of how it affects spermatozoa at the molecular level, especially in terms of non-coding RNAs. Therefore, we conducted this study, where we compared slow freezing and vitrification of good- and poor-quality human semen samples by analyzing conventional sperm quality parameters, performing functional tests and analyzing the expression of miRNAs. The results revealed that cryopreservation of normozoospermic samples does not alter the maturity of spermatozoa (protamine staining, hyaluronan binding), although cryopreservation can increase sperm DNA fragmentation and lower motility. On a molecular level, we revealed that in both types of cryopreservation, miRNAs from spermatozoa are significantly overexpressed compared to those in the native semen of normozoospermic patients, but in oligozoospermic samples, this effect is observed only after vitrification. Moreover, we show that expression of selected miRNAs is mostly overexpressed in native oligozoospermic samples compared to normozoospermic samples. Conversely, when vitrified normozoospermic and oligozoospermic samples were compared, we determined that only miR-99b-5p was significantly overexpressed in oligozoospermic sperm samples, and when comparing slow freezing, only miR-15b-5p and miR-34b3p were significantly under-expressed in oligozoospermic sperm samples. Therefore, our results imply that cryopreservation of normozoospermic sperm samples can modulate miRNA expression profiles in spermatozoa to become comparable to those in oligozoospermic samples.
Keywords:semen, cryopreservation, vitrification, slow freezing, spermatozoa, microRNA, assisted reproduction, infertility
Publication status:Published
Publication version:Version of Record
Year of publishing:2024
Number of pages:str. 1-23
Numbering:Vol. 25, iss. 8, [article no.] 4157
PID:20.500.12556/DiRROS-29963 New window
UDC:61
ISSN on article:1422-0067
DOI:10.3390/ijms25084157 New window
COBISS.SI-ID:191979267 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 9. 4. 2024;
Publication date in DiRROS:10.06.2026
Views:80
Downloads:72
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Record is a part of a journal

Title:International journal of molecular sciences
Shortened title:Int. j. mol. sci.
Publisher:MDPI
ISSN:1422-0067
COBISS.SI-ID:2779162 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J3-2531-2020
Name:Vpliv počasnega zamrzovanja in vitrifikacije na izražanje miRNA v humanih semenčicah

Funder:Other - Other funder or multiple funders
Funding programme:Univerzitetni klinični center Ljubljana
Project number:20210024
Name:Vpliv počasnega zamrzovanja in vitrifikacije na izražanje miRNA v humanih semenčicah

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:seme, kriokonzervacija, vitrifikacija, počasno zamrzovanje, semenčice, mikroRNA, asistirana reprodukcija, neplodnost


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