Na+/H+-exchange activity and immunolocalization of NHE3 in rat epididymis
Corinne Bagnis, Mireille Marsolais, Daniel Biemesderfer, Raynald Laprade, Sylvie Breton
2001
AJP - Renal Physiology
Bagnis, Corinne, Mireille Marsolais, Daniel Biemesderfer, Raynald Laprade, and Sylvie Breton. Na ϩ /H ϩexchange activity and immunolocalization of NHE3 in rat epididymis. Am J Physiol Renal Physiol 280: F426-F436, 2001.-An acidic luminal pH in the epididymis and vas deferens (VD) helps maintain mature sperm in an immotile state during storage. We have previously shown that the majority of proton secretion in the VD is due to the activity of the vacuolar H ϩ -ATPase. Acidification is dependent
more »
... luminal sodium in more proximal regions of the epididymis, and we examined the distribution of the Na ϩ /H ϩ exchanger, NHE3, by immunofluorescence and measured Na ϩ /H ϩ exchange (NHE) activity in isolated epididymal tubules. NHE3 was detected in the apical pole of nonciliated cells of the efferent ducts and principal cells (PC) of the epididymis. No staining was seen in the distal cauda epididymidis and the VD. Isolated tubules from the distal initial segment (DIS) and proximal cauda epididymidis were perfused in vitro and loaded with the pH-sensitive dye 2Ј,7Ј-bis(carboxyethyl)-5(6Ј)-carboxyfluorescein. Ethylisopropyl amiloride (EIPA) (50 M) reduced the initial rate of intracellular pH recovery (dpH i /dt), in response to an acute acid load, by 51% and 45% in the DIS and cauda epididymidis, respectively. In the DIS, removal of luminal sodium reduced dpH i /dt by 52%. HOE694 (50 M) inhibited all EIPA-sensitive dpH i /dt in the DIS, despite the previously reported absence of NHE2 in this region (Cheng Chew SB, Leung GPH, Leung PY, Tse CM, and Wong PYD, Biol Reprod 62: 755-758, 2000). These data indicate that HOE694-and EIPA-sensitive Na ϩ /H ϩ exchange may participate, together with the H ϩ -ATPase, in luminal acidification in the male excurrent duct. male reproductive tract; transepithelial acid-base transport; acidification; immunofluorescence; intracellular pH. Address for reprint requests and other correspondence: Sylvie Breton, Renal Unit and Program in Membrane Biology, Massachusetts General Hospital East, 149 13th St.,
doi:10.1152/ajprenal.2001.280.3.f426
pmid:11181404
fatcat:k4vburb635ctxgkm7p4dbvqwzq