Pace A J, Lee E, Athirakul K, Coffman T M, O'Brien D A, Koller B H
Curriculum in Genetics, Department of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Clin Invest. 2000 Feb;105(4):441-50. doi: 10.1172/JCI8553.
The Na(+)-K(+)-2Cl(-) cotransporter (NKCC1) carries 1 molecule of Na(+) and K(+) along with 2 molecules of Cl(-) across the cell membrane. It is expressed in a broad spectrum of tissues and has been implicated in cell volume regulation and in ion transport by secretory epithelial tissue. However, the specific contribution of NKCC1 to the physiology of the various organ systems is largely undefined. We have generated mouse lines carrying either of 2 mutant alleles of the Slc12a2 gene, which encodes this cotransporter: a null allele and a mutation that results in deletion of 72 amino acids of the cytoplasmic domain. Both NKCC1-deficient mouse lines show behavioral abnormalities characteristic of mice with inner ear defects. Male NKCC1-deficient mice are infertile because of defective spermatogenesis, as shown by the absence of spermatozoa in histological sections of their epididymides and the small number of spermatids in their testes. Consistent with this observation, we show that Slc12a2 is expressed in Sertoli cells, pachytene spermatocytes, and round spermatids isolated from wild-type animals. Our results indicate a critical role for NKCC1-mediated ion transport in spermatogenesis and suggest that the cytoplasmic domain of NKCC1 is essential in the normal functioning of this protein.
钠-钾-2氯协同转运蛋白(NKCC1)携带1分子的Na⁺和K⁺以及2分子的Cl⁻穿过细胞膜。它在多种组织中表达,并参与细胞体积调节以及分泌上皮组织的离子转运。然而,NKCC1对各种器官系统生理学的具体贡献在很大程度上尚不清楚。我们构建了携带Slc12a2基因两个突变等位基因之一的小鼠品系,该基因编码这种协同转运蛋白:一个无效等位基因和一个导致胞质结构域72个氨基酸缺失的突变。两个NKCC1缺陷小鼠品系均表现出内耳缺陷小鼠特有的行为异常。雄性NKCC1缺陷小鼠不育,原因是精子发生缺陷,这从其附睾组织切片中无精子以及睾丸中少量精子细胞可以看出。与此观察结果一致,我们发现Slc12a2在从野生型动物分离的支持细胞、粗线期精母细胞和圆形精子细胞中表达。我们的结果表明NKCC1介导的离子转运在精子发生中起关键作用,并表明NKCC1的胞质结构域对该蛋白的正常功能至关重要。