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Unlocking the Mystery of Male Infertility: Indian Scientists Discover Key Protein for Sperm Motility

  • Nishadil
  • September 12, 2025
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  • 2 minutes read
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Unlocking the Mystery of Male Infertility: Indian Scientists Discover Key Protein for Sperm Motility

A groundbreaking discovery from India is set to revolutionize our understanding and treatment of male infertility. Researchers have pinpointed a crucial protein, CFAP91, as a vital player in sperm motility, offering a new beacon of hope for countless couples struggling to conceive.

For too long, male infertility has been a complex and often misunderstood challenge, with a significant percentage of cases remaining unexplained.

One of the primary culprits is asthenozoospermia, a condition characterized by reduced sperm motility, where sperm struggle to swim effectively towards the egg. This new study from the Centre for Cellular and Molecular Biology (CCMB) in Hyderabad, in collaboration with other prominent institutions, sheds much-needed light on this enigmatic issue.

The scientists discovered that the CFAP91 protein is absolutely essential for the proper formation and function of the sperm's flagellum – its tail.

Think of the flagellum as the engine that propels the sperm forward on its arduous journey. Without a perfectly functioning CFAP91 protein, this intricate engine malfunctions, leading to severely impaired movement or even complete immotility.

Dr. K. Thangaraj, a lead researcher in the study, emphasized the protein's critical role.

The team meticulously studied individuals suffering from asthenozoospermia and found that mutations in the CFAP91 gene were directly responsible for the defects observed in their sperm tails. These genetic anomalies prevented the protein from performing its job, essentially grounding the sperm before it could even begin its mission.

This discovery is not merely an academic breakthrough; it holds profound implications for clinical practice.

Currently, diagnosing the precise genetic causes of male infertility can be challenging. Identifying CFAP91 as a key factor opens up new avenues for more accurate and targeted diagnostics. Genetic screening for CFAP91 mutations could become a standard procedure, offering clarity to couples and guiding personalized treatment plans.

Furthermore, this research paves the way for potential therapeutic interventions.

While direct gene therapy for sperm might be a long-term goal, understanding the molecular mechanisms behind CFAP91's function could lead to pharmacological approaches or assisted reproductive technologies (ART) that specifically address these genetic defects. It also provides invaluable information for genetic counseling, helping couples understand their risk factors and make informed decisions about family planning.

The study highlights the increasing capabilities of Indian science on the global stage, contributing significantly to a critical area of human health.

By unraveling the mysteries of CFAP91, these dedicated researchers have gifted the world a powerful new tool in the fight against male infertility, bringing hope and possibilities to families worldwide.

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