Abstract
1. Primary monolayer cultures from adult human epididymis were grown on Petri dishes and previous supports. The epithelia so formed were used for whole-cell patch clamp recording and short-circuit current (ISC) measurement. 2. After 50 days of culture, the cells formed a tight epithelium with transepithelial potential of 5.5 +/- 1.3 mV (mean +/- S.E.M.., n = 16), apical side negative, and a basal ISC of 6.9 +/- 0.9 microA cm-2 (mean +/- S.E.M., n = 16). 3. Adrenaline, when added to the basolateral side, at a concentration of 0.23 mumol l-1 increased the ISC by 3.0 +/- 1.2 microA cm-2 (mean +/- S.E.M., n = 4). This increase was blockable by diphenylamine-2-carboxylate (DPC, 1 mmol l-1). Forskolin (10 mumol l-1) also evoked a similar response to adrenaline. 4. In whole-cell patch clamp experiment, the resting membrane potential of the cells after dialysis with pipette solution containing 135 mmol l-1 KCl was found to be -30 +/- 14 mV (mean +/- S.E.M., n = 15). 5. About 90% of the cells successfully forming patches responded to 1 mumol l-1 adrenaline by an increase in inward current at -70 mV holding potential (delta I = -1600 +/- 900 pA, mean +/- S.E.M., n = 15). This increase in current was accompanied by a shift in reversal potential to -2 +/- 1 mV (mean +/- S.E.M., n = 15). 6. The adrenaline-induced inward current was found to be blockable by the Cl- channel blocker, DPC (0.25 mmol l-1). Ion substitution experiments showed that the adrenaline-evoked current was carried mainly by Cl-. 7. The effect of adrenaline on the whole-cell current was found to be mimicked by forskolin and could be abolished by including GDP beta S or a protein kinase A inhibitor in the pipette solution. Propranolol, but not phentolamine, completely abolished the effect of adrenaline. 8. Inclusion of 20 mmol l-1 EGTA or 2 mmol l-1 BAPTA + 100 mumol l-1 TMB-8 (to inhibit intracellular Ca2+ release) in the pipette did not seem to have any marked effect on adrenaline-evoked whole-cell current. Lowering the pipette Ca2+ concentration to 1 nmol l-1 or raising it to 10 mumol l-1 had no effect on the whole-cell current response to adrenaline. 9. This study shows that adrenaline stimulates Cl- secretion in cultured human epididymal cells.(ABSTRACT TRUNCATED AT 400 WORDS)
Full text
PDF














Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cliff W. H., Frizzell R. A. Separate Cl- conductances activated by cAMP and Ca2+ in Cl(-)-secreting epithelial cells. Proc Natl Acad Sci U S A. 1990 Jul;87(13):4956–4960. doi: 10.1073/pnas.87.13.4956. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cook D. I., Day M. L., Champion M. P., Young J. A. Ca2+ not cyclic AMP mediates the fluid secretory response to isoproterenol in the rat mandibular salivary gland: whole-cell patch-clamp studies. Pflugers Arch. 1988 Nov;413(1):67–76. doi: 10.1007/BF00581230. [DOI] [PubMed] [Google Scholar]
- Cooper T. G., Yeung C. H., Meyer R., Schulze H. Maintenance of human epididymal epithelial cell function in monolayer culture. J Reprod Fertil. 1990 Sep;90(1):81–91. doi: 10.1530/jrf.0.0900081. [DOI] [PubMed] [Google Scholar]
- Cuthbert A. W., Wong P. Y. Electrogenic anion secretion in cultured rat epididymal epithelium. J Physiol. 1986 Sep;378:335–345. doi: 10.1113/jphysiol.1986.sp016222. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fenwick E. M., Marty A., Neher E. A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol. 1982 Oct;331:577–597. doi: 10.1113/jphysiol.1982.sp014393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
- Levitzki A. From epinephrine to cyclic AMP. Science. 1988 Aug 12;241(4867):800–806. doi: 10.1126/science.2841758. [DOI] [PubMed] [Google Scholar]
- Marty A., Tan Y. P., Trautmann A. Three types of calcium-dependent channel in rat lacrimal glands. J Physiol. 1984 Dec;357:293–325. doi: 10.1113/jphysiol.1984.sp015501. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller D. J., Smith G. L. EGTA purity and the buffering of calcium ions in physiological solutions. Am J Physiol. 1984 Jan;246(1 Pt 1):C160–C166. doi: 10.1152/ajpcell.1984.246.1.C160. [DOI] [PubMed] [Google Scholar]
- Morris A. P., Gallacher D. V., Irvine R. F., Petersen O. H. Synergism of inositol trisphosphate and tetrakisphosphate in activating Ca2+-dependent K+ channels. Nature. 1987 Dec 17;330(6149):653–655. doi: 10.1038/330653a0. [DOI] [PubMed] [Google Scholar]
- Petersen O. H., Maruyama Y. Calcium-activated potassium channels and their role in secretion. Nature. 1984 Feb 23;307(5953):693–696. doi: 10.1038/307693a0. [DOI] [PubMed] [Google Scholar]
- Pollard C. E., Harris A., Coleman L., Argent B. E. Chloride channels on epithelial cells cultured from human fetal epididymis. J Membr Biol. 1991 Dec;124(3):275–284. doi: 10.1007/BF01994360. [DOI] [PubMed] [Google Scholar]
- Sato K., Sato F. Cholinergic potentiation of isoproterenol-induced cAMP level in sweat gland. Am J Physiol. 1983 Sep;245(3):C189–C195. doi: 10.1152/ajpcell.1983.245.3.C189. [DOI] [PubMed] [Google Scholar]
- Taussig L. M., Lobeck C. C., di Sant'Agnese P. A., Ackerman D. R., Kattwinkel J. Fertility in males with cystic fibrosis. N Engl J Med. 1972 Sep 21;287(12):586–589. doi: 10.1056/NEJM197209212871204. [DOI] [PubMed] [Google Scholar]
- Trautmann A., Marty A. Activation of Ca-dependent K channels by carbamoylcholine in rat lacrimal glands. Proc Natl Acad Sci U S A. 1984 Jan;81(2):611–615. doi: 10.1073/pnas.81.2.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turner T. T. On the epididymis and its function. Invest Urol. 1979 Mar;16(5):311–321. [PubMed] [Google Scholar]
- Wong P. Y. Control of anion and fluid secretion by apical P2-purinoceptors in the rat epididymis. Br J Pharmacol. 1988 Dec;95(4):1315–1321. doi: 10.1111/j.1476-5381.1988.tb11770.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wong P. Y., Fu W. O., Huang S. J., Law W. K. Effect of angiotensins on electrogenic anion transport in monolayer cultures of rat epididymis. J Endocrinol. 1990 Jun;125(3):449–456. doi: 10.1677/joe.0.1250449. [DOI] [PubMed] [Google Scholar]
- Wong P. Y., Huang S. J. Secretory agonists stimulate a rise in intracellular cyclic AMP but not Ca2+ and inositol phosphates in cultured rat epididymal epithelium. Exp Physiol. 1990 May;75(3):321–337. doi: 10.1113/expphysiol.1990.sp003407. [DOI] [PubMed] [Google Scholar]
- Wong P. Y. Inhibition by chloride channel blockers of anion secretion in cultured epididymal epithelium and intact epididymis of rats. Br J Pharmacol. 1988 May;94(1):155–163. doi: 10.1111/j.1476-5381.1988.tb11510.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wong P. Y. Mechanism of adrenergic stimulation of anion secretion in cultured rat epididymal epithelium. Am J Physiol. 1988 Jan;254(1 Pt 2):F121–F133. doi: 10.1152/ajprenal.1988.254.1.F121. [DOI] [PubMed] [Google Scholar]
- Wong P. Y. Potassium channel blockers inhibit anion secretion in cultured rat epididymal epithelium. Jpn J Physiol. 1989;39(4):595–607. doi: 10.2170/jjphysiol.39.595. [DOI] [PubMed] [Google Scholar]
- Wong P. Y., Uchendu C. N. Studies on the renin-angiotensin system in primary monolayer cell cultures of the rat epididymis. J Endocrinol. 1991 Nov;131(2):287–293. doi: 10.1677/joe.0.1310287. [DOI] [PubMed] [Google Scholar]
- Wong P. Y., Uchendu C. N. The role of angiotensin-converting enzyme in the rat epididymis. J Endocrinol. 1990 Jun;125(3):457–465. doi: 10.1677/joe.0.1250457. [DOI] [PubMed] [Google Scholar]
- Wong P. Y., Yeung C. H. Hormonal regulation of fluid reabsorption in isolated rat cauda epididymidis. Endocrinology. 1977 Nov;101(5):1391–1397. doi: 10.1210/endo-101-5-1391. [DOI] [PubMed] [Google Scholar]
