Department of Laboratory Medicine,College of Medicine,The Catholic University of Korea,Seoul,Republic of Korea.
Instituto de Biología y Medicina Experimental (IByME-CONICET), Ciudad Autónoma de Buenos Aires, Argentina.
Biol Reprod. 2017 Feb 1;96(2):366-375. doi: 10.1095/biolreprod.116.144857.
While spermatozoa undergo epididymal maturation, they remain quiescent thanks to the establishment of a low luminal pH. This study is aimed at determining how epithelial cells lining the epididymal lumen work together to maintain and regulate this acidic milieu. In particular, we examined the relative contribution of clear cells (CCs) and principal cells (PCs) to this process. Functional analysis in the mouse cauda epididymidis (Cd) perfused in vivo showed that the pH of a control solution remained constant at pH 6.6 after perfusion through the Cd lumen. In contrast, the pH of both an acidic (pH 5.8) and alkaline (pH 7.8) perfusate was progressively restored toward the control acidic pH. Pharmacological studies indicated the contribution of cystic fibrosis transmembrane regulator, previously shown to be present in the apical membrane of PCs, to the recovery from an acidic pH of 5.8. In addition, we found that CCs and PCs equally contribute to the recovery from an alkaline of 7.8, via the H+ pumping vacuolar ATPase (V-ATPase) located in CCs, and the Na+/H+ exchanger type 3 (NHE3) located in PCs. Immunofluorescence labeling showed apical membrane accumulation of the V-ATPase in CCs at pH 7.8, and its internalization at pH 5.8 compared to pH 6.6. Immunofluorescence showed expression of NHE3, but absence of NHE2, in PCs located in the Cd. RT-PCR and western blotting showed expression of NHE3 in all epididymal regions. Luminal 8-(4-chlorophenylthio)adenosine 3΄,5΄-cyclic monophosphate (cpt-cAMP) partially inhibited luminal pH recovery from pH 7.8. However, cpt-cAMP induced an increase in V-ATPase apical membrane accumulation at this pH. Cell fractionation studies showed the apical accumulation of NHE3 from intracellular vesicles at pH 7.8 versus 6.6, and prevention of this effect by cpt-cAMP. These results indicate the participation of both CCs and PCs in the regulation of luminal pH in the epididymis. Our study also shows the dual role of PCs in HCO3− and H+ secretion, and that this switch from base to acid secretion depends on the luminal environment. Characterization of the respective roles of CCs and PCs in the regulation of the optimal luminal condition for epididymal sperm maturation should provide new frameworks for the evaluation and treatment of male infertility.
在精子经历附睾成熟的过程中,由于管腔中建立了低 pH 值环境,精子处于静止状态。本研究旨在确定附睾管腔衬里上皮细胞如何共同维持和调节这种酸性环境。特别是,我们研究了透明细胞 (CCs) 和主细胞 (PCs) 在这个过程中的相对贡献。在体内灌流的小鼠附睾尾 (Cd) 中的功能分析表明,对照溶液的 pH 值在通过 Cd 管腔灌流后仍保持在 6.6 的恒定 pH 值。相比之下,酸性 (pH 5.8) 和碱性 (pH 7.8) 灌流液的 pH 值均逐渐恢复到对照酸性 pH 值。药理学研究表明,囊性纤维化跨膜转导调节蛋白 (CFTR) 发挥作用,CFTR 先前被证明存在于 PCs 的顶膜上,有助于从酸性 pH 值 5.8 中恢复。此外,我们发现 CCs 和 PCs 同样通过位于 CCs 的 H+ 泵Vacuolar ATPase (V-ATPase) 和位于 PCs 的 Na+/H+ 交换体 3 (NHE3) ,对碱性 pH 值 7.8 的恢复做出贡献。免疫荧光标记显示,在 pH 值为 7.8 时,CCs 的顶膜积聚 V-ATPase,而在 pH 值为 5.8 时与 pH 值 6.6 相比则内化。免疫荧光显示,位于 Cd 中的 PCs 表达 NHE3,但不存在 NHE2。RT-PCR 和 Western blot 显示,NHE3 在所有附睾区域均有表达。腔内 8-(4-氯苯硫基)腺苷 3′,5′-环单磷酸 (cpt-cAMP) 部分抑制了从 pH 值 7.8 恢复到 pH 值的腔管 pH 值。然而,cpt-cAMP 在这个 pH 值下诱导 V-ATPase 顶膜积聚增加。细胞分级研究显示,与 pH 值 6.6 相比,NHE3 从胞内囊泡中在 pH 值 7.8 时顶膜积聚,cpt-cAMP 可阻止这种效应。这些结果表明 CCs 和 PCs 均参与了附睾管腔 pH 值的调节。我们的研究还表明,PCs 在 HCO3−和 H+分泌中发挥双重作用,这种从基础到酸分泌的转变取决于管腔环境。阐明 CCs 和 PCs 在调节附睾精子成熟的最佳腔管条件中的各自作用,应为男性不育症的评估和治疗提供新的框架。