The Importance of AKR1B10, A Key Regulator of Spermatid Germplasm, for Human Fertility and Disease
The Importance of AKR1B10, A Key Regulator of Spermatid Germplasm, for Human Fertility and Disease
AKR1B10 (Alkylator-Activated Recipient 1 gene 1 protein) is a gene that encodes a protein known as HSI (histone sperminyltransferase inhibitor). HSI plays a critical role in the regulation of male fertility by preventing the transfer of spermatozoa from the testes to the epididymis, where they would cause damage to the vas deferens. In addition, HSI has also been shown to have potential as a drug target and biomarker for several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.
The Importance of AKR1B10
AKR1B10 is a key regulator of spermatid germplasm, which is the component of sperm that carries genetic information from the father to the child. In humans, spermatid germplasm is generated in the testes and meiosis, and it consists of approximately 250 million microscopic spermatids. The function of these spermatids is to produce spermatozoa, which are the genetic units of the male sex.
AKR1B10 is the gene that encodes the HSI protein. This protein is critical for the regulation of spermatid germplasm and the production of healthy spermatozoa. HSI plays a vital role in preventing the transfer of spermatozoa from the testes to the epididymis, where they would cause damage to the vas deferens. This protein also helps to ensure that only healthy spermatozoa are released from the testes and are able to fertilize the eggs.
In addition to its role in spermatid germplasm, HSI has also been shown to have potential as a drug target and biomarker for several diseases. For example, studies have shown that HSI can be overexpressed in various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. This suggests that HSI may be a useful biomarker for these diseases and may also be a potential drug target.
The Potential of AKR1B10 as a Drug Target
AKR1B10 has been shown to be a potential drug target for several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. One of the main reasons for its potential as a drug target is its involvement in the regulation of spermatid germplasm and the production of healthy spermatozoa.
For example, studies have shown that HSI can be overexpressed in various diseases, including cancer. This suggests that increasing the levels of HSI in the body may make these diseases more resistant to treatment. In addition, HSI has also been shown to be involved in the regulation of cell division and apoptosis, which are important processes that are affected in many diseases.
Another potential mechanism by which AKR1B10 may be a drug target is its role in the regulation of immune responses. Studies have shown that HSI can be overexpressed in various autoimmune disorders, including rheumatoid arthritis, lupus, and multiple sclerosis. This suggests that HSI may be involved in the regulation of the immune response and may be a potential target for drugs that are used to treat these disorders.
The Potential of AKR1B10 as a Biomarker
AKR1B10 has also been shown to have potential as a biomarker for several diseases. For example, studies have shown that the levels of HSI in the testes are significantly lower in men with certain forms of cancer, such as prostate cancer, than in men without these diseases. This suggests that HSI may be a potential biomarker for these diseases and may be able to be used as a diagnostic tool.
In addition, HSI has also been shown to be involved in
Protein Name: Aldo-keto Reductase Family 1 Member B10
Functions: Catalyzes the NADPH-dependent reduction of a wide variety of carbonyl-containing compounds to their corresponding alcohols (PubMed:9565553, PubMed:18087047, PubMed:12732097, PubMed:19013440, PubMed:19563777). Displays strong enzymatic activity toward all-trans-retinal, 9-cis-retinal, and 13-cis-retinal (PubMed:12732097, PubMed:18087047). Plays a critical role in detoxifying dietary and lipid-derived unsaturated carbonyls, such as crotonaldehyde, 4-hydroxynonenal, trans-2-hexenal, trans-2,4-hexadienal and their glutathione-conjugates carbonyls (GS-carbonyls) (PubMed:19013440, PubMed:19563777). Displays no reductase activity towards glucose (PubMed:12732097)
More Common Targets
AKR1B10P1 | AKR1B15 | AKR1C1 | AKR1C2 | AKR1C3 | AKR1C4 | AKR1C6P | AKR1C8 | AKR1D1 | AKR1E2 | AKR7A2 | AKR7A2P1 | AKR7A3 | AKR7L | AKT1 | AKT1S1 | AKT2 | AKT3 | AKTIP | ALAD | ALAS1 | ALAS2 | ALB | ALCAM | Alcohol Dehydrogenase | Alcohol dehydrogenase Class 1 | Aldehyde Dehydrogenase | ALDH16A1 | ALDH18A1 | ALDH1A1 | ALDH1A2 | ALDH1A3 | ALDH1A3-AS1 | ALDH1B1 | ALDH1L1 | ALDH1L1-AS1 | ALDH1L2 | ALDH2 | ALDH3A1 | ALDH3A2 | ALDH3B1 | ALDH3B2 | ALDH4A1 | ALDH5A1 | ALDH6A1 | ALDH7A1 | ALDH8A1 | ALDH9A1 | Aldo-Keto Reductase Family 1 | ALDOA | ALDOAP2 | ALDOB | ALDOC | ALG1 | ALG10 | ALG10B | ALG11 | ALG12 | ALG13 | ALG14 | ALG1L10P | ALG1L13P | ALG1L1P | ALG1L2 | ALG1L5P | ALG1L7P | ALG1L8P | ALG2 | ALG3 | ALG5 | ALG6 | ALG8 | ALG9 | ALK | ALKAL1 | ALKAL2 | Alkaline Phosphatase (ALP) | ALKBH1 | ALKBH2 | ALKBH3 | ALKBH4 | ALKBH5 | ALKBH6 | ALKBH7 | ALKBH8 | ALLC | ALMS1 | ALMS1-IT1 | ALMS1P1 | ALOX12 | ALOX12-AS1 | ALOX12B | ALOX12P2 | ALOX15 | ALOX15B | ALOX15P1 | ALOX15P2 | ALOX5 | ALOX5AP | ALOXE3