Mitochondria-related miR-151a-5p reduces cellular ATP production by targeting CYTB in asthenozoospermia

Ran Zhou1,2, Rong Wang3, Yufeng Qin1,2

  • 1State Key Laboratory of Reproductive Medicine, Institute of Toxicology, Nanjing Medical University, Nanjing 210029, China.

Scientific Reports
|December 3, 2015
PubMed

Insights

Mitochondria-related microRNAs (miRNAs) are linked to sperm health. This study found miR-151a-5p may impair sperm energy production by reducing mitochondrial function and ATP levels in asthenozoospermia.

Area of Science:

  • Mitochondrial biology
  • Molecular genetics
  • Reproductive medicine

Background:

  • Mitochondria are crucial for sperm viability and energy metabolism.
  • Mitochondria-related microRNAs (miRNAs) may regulate mitochondrial function.
  • Asthenozoospermia, characterized by poor sperm motility, impacts male fertility.

Purpose of the Study:

  • To investigate the role of mitochondria-related miRNAs in asthenozoospermia.
  • To identify specific miRNAs associated with severe asthenozoospermia.
  • To elucidate the functional impact of identified miRNAs on mitochondrial function.

Main Methods:

  • Screening of seminal plasma miRNAs using TaqMan Low Density Array (TLDA).
  • Validation of miRNA expression levels via quantitative reverse transcriptase polymerase chain reaction (qRT-PCR).
  • Functional analysis of miRNA effects on mitochondrial function in GC-2 cells.

Main Results:

  • Significant alterations in seminal plasma miRNA profiles were observed in severe asthenozoospermia.
  • miR-101-3p and let-7b-5p were decreased, while miR-151a-5p was increased in asthenozoospermia cases.
  • Overexpression of miR-151a-5p reduced mitochondrial respiratory activity, Adenosine Triphosphate (ATP) levels, and Cytochrome b (Cytb) expression.

Conclusions:

  • miR-151a-5p is significantly upregulated in severe asthenozoospermia.
  • miR-151a-5p negatively impacts mitochondrial function, cellular respiration, and ATP production.
  • miR-151a-5p may contribute to asthenozoospermia pathogenesis by targeting Cytochrome b (Cytb).

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