Hspa4l-Deficient Mice Display Increased Incidence of Male Infertility and Hydronephrosis Development
Hspa4l-Deficient Mice Display Increased Incidence of Male Infertility and Hydronephrosis Development
The Hspa4l gene, also known as Apg1 or Osp94, belongs to the HSP110 heat shock gene family, which includes three genes encoding highly conserved proteins. This study shows that Hspa4l is expressed ubiquitously and predominantly in the testis. The protein is highly expressed in spermatogenic cells, from late pachytene spermatocytes to postmeiotic spermatids. In the kidney, the protein is restricted to cortical segments of distal tubules. To study the physiological role of this gene in vivo, we generated mice deficient in Hspa4l by gene targeting. Hspa4l-deficient mice were born at expected ratios and appeared healthy. However, approximately 42% of Hspa4l(-/-) male mice suffered from fertility defects. Whereas the seminiferous tubules of Hspa4l(-/-) testes contained all stages of germ cells, the number of mature sperm in the epididymis and sperm motility were drastically reduced. The reduction of the sperm count was due to the elimination of a significant number of developing germ cells via apoptosis. No defects in fertility were observed in female mutants. In addition, 12% of null mutant mice developed hydronephrosis. Concentrations of plasma and urine electrolytes in Hspa4l(-/-) mice were similar to wild-type values, suggesting that the renal function was not impaired. However, Hspa4l(-/-) animals were preferentially susceptible to osmotic stress. These results provide evidence that Hspa4l is required for normal spermatogenesis and suggest that Hspa4l plays a role in osmotolerance.
- Hannover Medical School Germany
- LMU Klinikum Germany
- Institut für Humangenetik Germany
- Justus Liebig University Giessen Germany
- University of Göttingen Germany
Male, Mice, Knockout, Reproduction, Osmolar Concentration, Apoptosis, Hydronephrosis, Spermatozoa, Mice, Inbred C57BL, Mice, Germ Cells, Pregnancy, Gene Targeting, Testis, Animals, Female, HSP70 Heat-Shock Proteins, HSP90 Heat-Shock Proteins, HSP110 Heat-Shock Proteins, Spermatogenesis, Infertility, Male
Male, Mice, Knockout, Reproduction, Osmolar Concentration, Apoptosis, Hydronephrosis, Spermatozoa, Mice, Inbred C57BL, Mice, Germ Cells, Pregnancy, Gene Targeting, Testis, Animals, Female, HSP70 Heat-Shock Proteins, HSP90 Heat-Shock Proteins, HSP110 Heat-Shock Proteins, Spermatogenesis, Infertility, Male
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