Relationship between sperm telomere length and sperm quality in infertile men.
Zahra DarmishonnejadFarzaneh Zarei-KheirabadiMarziyeh TavalaeeMasoumeh Zarei-KheirabadiDina ZohrabiMohammad Hossein Nasr-EsfahaniPublished in: Andrologia (2020)
Telomeres, noncoding and repetitive DNA sequences play a significant function in chromatin integrity. Telomere length is age-dependent in somatic cells, while it increases in sperm cell with age. Therefore, we aimed to assess sperm chromatin, leucocyte and sperm telomere length (LTL, STL) in spermatozoon of 38 infertile and 19 fertile men aged between 20 and 50 years. Protamine deficiency (chromomycin A3 test), DNA fragmentation (TUNEL assay), lipid peroxidation (Bodipy probe) and telomere length (quantitative real-time PCR) were assessed. A significant decrease in mean of sperm concentration and motility and a significant increase in means of sperm abnormal morphology, DNA fragmentation, lipid peroxidation and protamine deficiency were observed in infertile compared with fertile men. In addition, the mean of LTL and STL were significantly shorter in infertile men compared with fertile individuals. We observed significant associations between telomere length with sperm concentration, DNA fragmentation and lipid peroxidation. We hypothesised that increased oxidative stress in spermatozoa of infertile men can result in abnormal packaging of chromatin, damage of DNA and shorter sperm telomere length. Together, these anomalies may account for fertility failure in these individuals.
Keyphrases
- circulating tumor
- oxidative stress
- single molecule
- cell free
- polycystic ovary syndrome
- dna damage
- gene expression
- middle aged
- transcription factor
- genome wide
- induced apoptosis
- fatty acid
- stem cells
- escherichia coli
- high throughput
- single cell
- signaling pathway
- young adults
- cystic fibrosis
- mass spectrometry
- pseudomonas aeruginosa
- staphylococcus aureus
- high frequency
- endoplasmic reticulum stress
- smoking cessation
- cell cycle arrest
- bone marrow
- genetic diversity
- childhood cancer