The Effects of Supplemented Coenzyme Q <sub>10</sub> to Extender on the Endoplasmic Reticulum Stress-Related Genes and Sperm Quality Parameters in Cryopreservation of Mouse Spermatozoa

The endoplasmic reticulum (ER) is the organelle responsible for protein folding in the cell. The damage that may occur during the freezing process of the sperm can exceed the protein loading capacity in the ER. Antioxidants, such as coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>), are added to freezing media to protect sperm cells. In this study, the aim was to investigate the expression levels of ER stress-related genes (protein kinase-like ER kinase [<i>PERK</i>], activating transcription factor 4 [<i>ATF4</i>], CCAAT-enhancer-binding-protein homologous protein [<i>CHOP</i>], and nuclear factor erythroid 2-related factor 2 [<i>NRF2</i>]) and quality parameters (viability, motility, acrosome status, and plasma membrane integrity) of mice sperm after freezing with an extender containing CoQ<sub>10</sub>. Male BALB/c mouse spermatozoa were cryopreserved using a combination of 18% raffinose + 3% skimmed milk and 50 µM CoQ<sub>10</sub>. The combination of 18% raffinose + 3% skimmed milk without CoQ<sub>10</sub> was used as the control group. The results showed that post-thaw sperm motility, viability, plasma membrane integrity, and intact acrosome rates were significantly higher in the CoQ<sub>10</sub>-supplemented group compared with the control (untreated) group (<i>p</i> < 0.05). The expression of ER stress-related genes was then analyzed to investigate whether CoQ<sub>10</sub> attenuates ER stress in frozen-thawed sperm. The results significantly revealed that the addition of 50 µM CoQ<sub>10</sub> to the extender increased <i>PERK</i>, <i>ATF4</i>, and <i>CHOP</i> mRNA levels compared with the control group (<i>p</i> < 0.001). Next, <i>NRF2</i> gene expression was analyzed to investigate whether CoQ<sub>10</sub> affects the antioxidant mechanism of post-thaw sperm. It was revealed that the expression of the <i>NRF2</i> gene significantly increased in the CoQ<sub>10</sub> group compared with the control group (<i>p</i> < 0.001). Collectively, these results suggest that the freeze-thaw process induces ER stress in mouse sperm, and the supplementation of CoQ<sub>10</sub> to the cryoprotectant agent reduces ER stress-related genes, activates the gene related to the antioxidant defense system, and improves post-thaw sperm quality parameters.

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Journal
Biopreservation and Biobanking
Published
2025-03-05
DOI
https://doi.org/10.1089/bio.2023.0084
Primary Topic
Sperm and Testicular Function
Type
article
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article

The Effects of Supplemented Coenzyme Q 10 to Extender on the Endoplasmic Reticulum Stress-Related Genes and Sperm Quality Parameters in Cryopreservation of Mouse Spermatozoa

Oğuz Kaan YALÇIN, Cengiz Yıldız, Aysel Eraslan Şakar, Ali Mazi
1 links
Biopreservation and Biobanking
Sperm and Testicular Function
article

The Effects of Supplemented Coenzyme Q 10 to Extender on the Endoplasmic Reticulum Stress-Related Genes and Sperm Quality Parameters in Cryopreservation of Mouse Spermatozoa

Oğuz Kaan YALÇIN, Cengiz Yıldız, Aysel Eraslan Şakar, Ali Mazi
article en

Abstract

The endoplasmic reticulum (ER) is the organelle responsible for protein folding in the cell. The damage that may occur during the freezing process of the sperm can exceed the protein loading capacity in the ER. Antioxidants, such as coenzyme Q<sub>10</sub> (CoQ<sub>10</sub>), are added to freezing media to protect sperm cells. In this study, the aim was to investigate the expression levels of ER stress-related genes (protein kinase-like ER kinase [<i>PERK</i>], activating transcription factor 4 [<i>ATF4</i>], CCAAT-enhancer-binding-protein homologous protein [<i>CHOP</i>], and nuclear factor erythroid 2-related factor 2 [<i>NRF2</i>]) and quality parameters (viability, motility, acrosome status, and plasma membrane integrity) of mice sperm after freezing with an extender containing CoQ<sub>10</sub>. Male BALB/c mouse spermatozoa were cryopreserved using a combination of 18% raffinose + 3% skimmed milk and 50 µM CoQ<sub>10</sub>. The combination of 18% raffinose + 3% skimmed milk without CoQ<sub>10</sub> was used as the control group. The results showed that post-thaw sperm motility, viability, plasma membrane integrity, and intact acrosome rates were significantly higher in the CoQ<sub>10</sub>-supplemented group compared with the control (untreated) group (<i>p</i> < 0.05). The expression of ER stress-related genes was then analyzed to investigate whether CoQ<sub>10</sub> attenuates ER stress in frozen-thawed sperm. The results significantly revealed that the addition of 50 µM CoQ<sub>10</sub> to the extender increased <i>PERK</i>, <i>ATF4</i>, and <i>CHOP</i> mRNA levels compared with the control group (<i>p</i> < 0.001). Next, <i>NRF2</i> gene expression was analyzed to investigate whether CoQ<sub>10</sub> affects the antioxidant mechanism of post-thaw sperm. It was revealed that the expression of the <i>NRF2</i> gene significantly increased in the CoQ<sub>10</sub> group compared with the control group (<i>p</i> < 0.001). Collectively, these results suggest that the freeze-thaw process induces ER stress in mouse sperm, and the supplementation of CoQ<sub>10</sub> to the cryoprotectant agent reduces ER stress-related genes, activates the gene related to the antioxidant defense system, and improves post-thaw sperm quality parameters.

Biopreservation and BiobankingVol. 23(5)
Mustafa Kemal University (TR)
Openalex Percentile: Top 93%
Sperm and Testicular Function
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