Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P56851 (epididymal)
 11,273 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Diets containing 0%, 5% and 10% protein were used for treatment periods of 30, 50, and 90 days respectively. Control rats were fed a diet containing 20% protein. Protein deficient rats failed to gain weight during the experiment. In addition, the weights of the testis, epididymis, prostate and seminal vesicle also decreased, with the 10% group less affected than the 0% and 5% groups. Testicular histology indicated retarded germ cell maturation in the 0% and 5% groups only. Overall testicular cell number and size were reduced in treated rats and there was a reduction in the diameter of the seminiferous tubule in these groups. Epididymal epithelial height was also reduced in protein deficient rats with a concomitant increase in the number of epididymal duct cross sections devoid of sperm. Protein deficiency caused significant reductions in testicular DNA, RNA and protein content. The proportion of motile epididymal sperm decreased in the 0% and 5% groups by 90% and 35% respectively. Epididymal sperm number decreased in both the 0% and 5% groups by 90% while the proportion of abnormal sperm increased by 65% and 61% respectively. Circulating androgen levels were also lowered by more than 50% on average in protein deficient animals.
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PMID:The effects of dietary protein deficiency on rat testicular function. 171 55

The aim of the present study is to analyse the relative and combined effects of ethanol and protein deficiency on serum testosterone and LH, and on gonadal histology, in ethanol fed rats. The study was performed in 32 animals divided into four groups, fed with the Lieber & DeCarli control, 36% ethanol, 2% protein, and 36% ethanol 2% protein containing diets, respectively. Two months later, rats were anaesthetized with pentobarbital and sacrificed, and the right testes and epididymus were carefully removed. Both ethanol and protein deficiency independently lead to a decrease in serum testosterone levels, and to testicular atrophy, lowest testosterone levels and highest degrees of atrophy being observed in the rats receiving the 36% ethanol, 2% protein containing diet. Both serum testosterone and testicular size and weight significantly correlated with final weight and serum albumin. Hypospermia, atrophy of the seminiferous tubules, and reduced epididymal diameter were also observed in this last group of animals. Thus, protein deficiency may contribute to hypogonadism of alcoholics.
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PMID:Relative and combined effects of ethanol and protein deficiency on gonadal function and histology. 781 91

While a large cohort of sperm surface receptors underpin sperm-oocyte adhesion processes, our recent work has revealed that the molecular chaperone Heat Shock Protein A2 (HSPA2) is a key regulator of zona pellucida-receptor complex assembly in our own species. Indeed, in the infertile population, spermatozoa that fail to interact with the zona pellucida of the oocyte consistently lack HSPA2 protein expression. While the mechanisms behind this protein deficiency are under consideration, BCL2-associated athanogene 6 (BAG6) has been identified as a key regulator of HSPA2 stability in mouse germ cells. However, in the human, the presence of BAG family proteins remains completely uncharacterized. Consequently, this study aimed to determine the presence of BAG6 in human sperm cells and to characterize its putative interaction with HSPA2 throughout sperm cell development. BAG6 was shown to co-localize with HSPA2 in human testicular germ cells and epididymal spermatozoa. Similarly, BAG6 was identified in the equatorial region of non-capacitated spermatozoa but underwent a marked relocation to the anterior region of the head upon the induction of capacitation in these cells. Protein-protein interaction assays revealed the stable interaction of BAG6 and HSPA2 proteins in mature spermatozoa. Furthermore, examination of the spermatozoa of infertile men with zona pellucida binding defects, related to a lack of HSPA2, revealed a concomitant deficiency in BAG6 protein expression. In view of the findings described in this study, we propose that BAG6 is likely a key regulator of HSPA2 stability/function in human germ cells. Moreover, its under-representation in spermatozoa with zona pellucida binding deficiency suggests that BAG6 may be an important candidate to study for a further understanding of male idiopathic infertility.
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PMID:Novel characterization of the HSPA2-stabilizing protein BAG6 in human spermatozoa. 2615 32