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Hspa4l基因缺陷型小鼠出现雄性不育和肾积水的发生率增加。

Hspa4l-deficient mice display increased incidence of male infertility and hydronephrosis development.

作者信息

Held Torsten, Paprotta Ilona, Khulan Janchiv, Hemmerlein Bernhardt, Binder Lutz, Wolf Stephan, Schubert Stephanie, Meinhardt Andreas, Engel Wolfgang, Adham Ibrahim M

机构信息

Institute of Human Genetics, University of Göttingen, Germany.

出版信息

Mol Cell Biol. 2006 Nov;26(21):8099-108. doi: 10.1128/MCB.01332-06. Epub 2006 Aug 21.

Abstract

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.

摘要

Hspa4l基因,也被称为Apg1或Osp94,属于HSP110热休克基因家族,该家族包含三个编码高度保守蛋白质的基因。本研究表明,Hspa4l在全身广泛表达,且在睾丸中表达最为显著。该蛋白在生精细胞中高度表达,从粗线期晚期精母细胞到减数分裂后精子细胞均有表达。在肾脏中,该蛋白仅限于远曲小管的皮质段。为了研究该基因在体内的生理作用,我们通过基因靶向技术构建了Hspa4l基因缺失的小鼠。Hspa4l基因缺失的小鼠按预期比例出生,外观健康。然而,约42%的Hspa4l(-/-)雄性小鼠存在生育缺陷。虽然Hspa4l(-/-)睾丸的生精小管中含有所有阶段的生殖细胞,但附睾中成熟精子的数量和精子活力却大幅降低。精子数量的减少是由于大量发育中的生殖细胞通过凋亡被清除。在雌性突变体中未观察到生育缺陷。此外,12%的基因敲除突变小鼠出现肾积水。Hspa4l(-/-)小鼠的血浆和尿液电解质浓度与野生型值相似,表明肾功能未受损。然而,Hspa4l(-/-)动物对渗透应激更为敏感。这些结果证明Hspa4l是正常精子发生所必需的,并表明Hspa4l在渗透压耐受性中发挥作用。

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