Yeung Ching-Hei, Breton Sylvie, Setiawan Iwan, Xu Yaoxian, Lang Florian, Cooper Trevor G
Institute of Reproductive Medicine, University of Münster, Domagkstrasse 11, D-48129 Münster, Germany.
Mol Reprod Dev. 2004 Jun;68(2):159-68. doi: 10.1002/mrd.20067.
Transgenic mice targeted for the c-ros gene, which are fertile when heterozygous (HET), but infertile when homozygous (knockout, KO) and associated with failure in pubertal differentiation of the epididymal initial segment, provide a model for studying the role of the epididymal luminal environment in sperm development. Luminal fluid from the cauda epididymidis was measured by both ion-selective microelectrodes and pH strips to be 0.3 pH units higher in the KO than HET. Of the genes responsible for luminal acidification, expression of mRNA of vacuolar H(+)-ATPase was found in all epididymal regions, but with no difference between KO and HET. Immunohistochemistry showed its presence in epithelial apical cells and clear cells. The Na(+)-hydrogen exchanger NHE2 was expressed at mRNA and protein levels in the caput but only marginally detectable if at all in the distal epididymis. This was compensated for by NHE3 which was expressed strongest in the cauda region, in agreement with immunohistochemical staining. Quantification of Western blot data revealed slight, but significant, decreases of NHE2 in the caput and of NHE3 in the cauda in the KO mice. The increase in luminal fluid pH in the KO mice could also be contributed to by other epithelial regulating factors including the Na(+)-dependent glutamate transporter EAAC1 formerly reported to be down regulated in the KO.
靶向c-ros基因的转基因小鼠,杂合子(HET)时可育,但纯合子(敲除,KO)时不育,且与附睾起始段青春期分化失败有关,为研究附睾管腔环境在精子发育中的作用提供了一个模型。通过离子选择性微电极和pH试纸测量附睾尾的管腔液,发现敲除小鼠的管腔液pH值比杂合子高0.3个pH单位。在负责管腔酸化的基因中,液泡H(+)-ATP酶的mRNA表达在所有附睾区域均有发现,但敲除小鼠和杂合子之间没有差异。免疫组织化学显示其存在于上皮顶端细胞和透明细胞中。钠氢交换体NHE2在附睾头的mRNA和蛋白质水平均有表达,但在附睾远端几乎检测不到。这由NHE3进行补偿,NHE3在附睾尾区域表达最强,这与免疫组织化学染色结果一致。对蛋白质印迹数据的定量分析显示,敲除小鼠附睾头的NHE2和附睾尾的NHE3均有轻微但显著的减少。敲除小鼠管腔液pH值的升高也可能由其他上皮调节因子导致,包括先前报道在敲除小鼠中下调的钠依赖性谷氨酸转运体EAAC1。