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. 1996 Jan 15;313(Pt 2):509–518. doi: 10.1042/bj3130509

Asymmetric signal transduction in polarized ileal Na(+)-absorbing cells: carbachol activates brush-border but not basolateral-membrane PIP2-PLC and translocates PLC-gamma 1 only to the brush border.

S Khurana 1, S Kreydiyyeh 1, A Aronzon 1, W A Hoogerwerf 1, S G Rhee 1, M Donowitz 1, M E Cohen 1
PMCID: PMC1216936  PMID: 8573085

Abstract

In ileal Na+ absorptive cells, carbachol inhibits NaCl absorption and its component brush-border Na+/H+ exchanger, acting via basolateral membrane (BLM) receptors. This carbachol effect involves brush-border but not BLM protein kinase C. In the present work we describe another asymmetric aspect of signal transduction in these epithelial cells, this time involving phosphatidylinositol 4,5-bisphosphate (PIP2)-specific phospholipase C (PLC). Thirty seconds and 1 min after carbachol treatment, brush-border PIP2-specific PLC activity increased, returning to control levels by 2.5 min. Involvement of brush-border tyrosine kinase(s) in this effect was suggested by inhibition of the carbachol effect on NaCl absorption by the tyrosine kinase inhibitor genistein, added to the mucosal but not the serosal surface. Luminal genistein pretreatment also prevented the carbachol-induced increase in brush-border PLC activity. In contrast, carbachol exposure did not change the BLM PIP2-specific PLC activity. Western analysis and immunoprecipitation demonstrated that PLC-gamma 1 is present in the brush border and that carbachol increases the PLC-gamma 1 amount in the brush border. Both the brush border and BLM contain PLC-beta 3 and a small amount of PLC-delta 1 but no PLC-beta 1, whereas BLM lacks detectable PLC-gamma 1. No change in PLC-beta 3 or PLC-delta 1 amount in the brush border occurred with carbachol exposure. No change in tyrosine phosphorylation of brush-border PLC-gamma 1 occurred with carbachol treatment. The Ca2+ ionophore A23187 did not alter PIP2-specific PLC activity in either the brush border or the BLM. These studies demonstrate that carbachol but not Ca2+ ionophore effects on brush-border NaCl absorption are associated with increases in brush-border but not BLM PIP2-specific PLC activity and in the amount of brush-border PLC-gamma 1, and involve tyrosine phosphorylation. This asymmetric aspect of epithelial signal transduction, together with the previous demonstration of localization of high-sensitivity IP3 stores to the apical membrane area in intestinal epithelial cells, shows that different aspects of signal transduction occur at the apical and basolateral membranes in epithelial and requires studies in both domains to define mechanisms of intracellular signalling.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALBERS R. W., RODRIGUEZDE LORES, DEROBERTIS E. SODIUM-POTASSIUM-ACTIVATED ATPASE AND POTASSIUM-ACTIVATED P-NITROPHENYLPHOSPHATASE: A COMPARISON OF THEIR SUBCELLULAR LOCALIZATIONS IN RAT BRAIN. Proc Natl Acad Sci U S A. 1965 Mar;53:557–564. doi: 10.1073/pnas.53.3.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abello J., Ye F., Bosshard A., Bernard C., Cuber J. C., Chayvialle J. A. Stimulation of glucagon-like peptide-1 secretion by muscarinic agonist in a murine intestinal endocrine cell line. Endocrinology. 1994 May;134(5):2011–2017. doi: 10.1210/endo.134.5.8156901. [DOI] [PubMed] [Google Scholar]
  3. Bartfai T. Preparation of metal-chelate complexes and the design of steady-state kinetic experiments involving metal nucleotide complexes. Adv Cyclic Nucleotide Res. 1979;10:219–242. [PubMed] [Google Scholar]
  4. Berstein G., Blank J. L., Smrcka A. V., Higashijima T., Sternweis P. C., Exton J. H., Ross E. M. Reconstitution of agonist-stimulated phosphatidylinositol 4,5-bisphosphate hydrolysis using purified m1 muscarinic receptor, Gq/11, and phospholipase C-beta 1. J Biol Chem. 1992 Apr 25;267(12):8081–8088. [PubMed] [Google Scholar]
  5. Botfield M. C., Naguchi K., Tsuchiya T., Wilson T. H. Membrane topology of the melibiose carrier of Escherichia coli. J Biol Chem. 1992 Jan 25;267(3):1818–1822. [PubMed] [Google Scholar]
  6. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  7. Bredt D. S., Mourey R. J., Snyder S. H. A simple, sensitive, and specific radioreceptor assay for inositol 1,4,5-trisphosphate in biological tissues. Biochem Biophys Res Commun. 1989 Mar 31;159(3):976–982. doi: 10.1016/0006-291x(89)92204-3. [DOI] [PubMed] [Google Scholar]
  8. Chang E. B., Musch M. W. Calcium mediated neurohumoral inhibition of chicken enterocyte Na influx: role of phosphatidylinositol metabolites. Life Sci. 1990;46(26):1913–1921. doi: 10.1016/0024-3205(90)90506-m. [DOI] [PubMed] [Google Scholar]
  9. Cohen M. E., Wesolek J., McCullen J., Rys-Sikora K., Pandol S., Rood R. P., Sharp G. W., Donowitz M. Carbachol- and elevated Ca(2+)-induced translocation of functionally active protein kinase C to the brush border of rabbit ileal Na+ absorbing cells. J Clin Invest. 1991 Sep;88(3):855–863. doi: 10.1172/JCI115387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dickinson K. E., Frizzell R. A., Sekar M. C. Activation of T84 cell chloride channels by carbachol involves a phosphoinositide-coupled muscarinic M3 receptor. Eur J Pharmacol. 1992 Apr 10;225(4):291–298. doi: 10.1016/0922-4106(92)90102-2. [DOI] [PubMed] [Google Scholar]
  11. Donowitz M., Cohen M. E., Gould M., Sharp G. W. Elevated intracellular Ca2+ acts through protein kinase C to regulate rabbit ileal NaCl absorption. Evidence for sequential control by Ca2+/calmodulin and protein kinase C. J Clin Invest. 1989 Jun;83(6):1953–1962. doi: 10.1172/JCI114104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Donowitz M., Emmer E., McCullen J., Reinlib L., Cohen M. E., Rood R. P., Madara J., Sharp G. W., Murer H., Malmstrom K. Freeze-thaw and high-voltage discharge allow macromolecule uptake into ileal brush-border vesicles. Am J Physiol. 1987 Jun;252(6 Pt 1):G723–G735. doi: 10.1152/ajpgi.1987.252.6.G723. [DOI] [PubMed] [Google Scholar]
  13. Goldschmidt-Clermont P. J., Kim J. W., Machesky L. M., Rhee S. G., Pollard T. D. Regulation of phospholipase C-gamma 1 by profilin and tyrosine phosphorylation. Science. 1991 Mar 8;251(4998):1231–1233. doi: 10.1126/science.1848725. [DOI] [PubMed] [Google Scholar]
  14. Jhon D. Y., Lee H. H., Park D., Lee C. W., Lee K. H., Yoo O. J., Rhee S. G. Cloning, sequencing, purification, and Gq-dependent activation of phospholipase C-beta 3. J Biol Chem. 1993 Mar 25;268(9):6654–6661. [PubMed] [Google Scholar]
  15. Jhon D. Y., Lee H. H., Park D., Lee C. W., Lee K. H., Yoo O. J., Rhee S. G. Cloning, sequencing, purification, and Gq-dependent activation of phospholipase C-beta 3. J Biol Chem. 1993 Mar 25;268(9):6654–6661. [PubMed] [Google Scholar]
  16. Kachintorn U., Vajanaphanich M., Barrett K. E., Traynor-Kaplan A. E. Elevation of inositol tetrakisphosphate parallels inhibition of Ca(2+)-dependent Cl- secretion in T84 cells. Am J Physiol. 1993 Mar;264(3 Pt 1):C671–C676. doi: 10.1152/ajpcell.1993.264.3.C671. [DOI] [PubMed] [Google Scholar]
  17. Kasai H., Augustine G. J. Cytosolic Ca2+ gradients triggering unidirectional fluid secretion from exocrine pancreas. Nature. 1990 Dec 20;348(6303):735–738. doi: 10.1038/348735a0. [DOI] [PubMed] [Google Scholar]
  18. Kasai H., Li Y. X., Miyashita Y. Subcellular distribution of Ca2+ release channels underlying Ca2+ waves and oscillations in exocrine pancreas. Cell. 1993 Aug 27;74(4):669–677. doi: 10.1016/0092-8674(93)90514-q. [DOI] [PubMed] [Google Scholar]
  19. Komabayashi T., Yakata A., Izawa T., Fujinami H., Suda K., Tsuboi M. Mechanism of carbachol-stimulated diacylglycerol formation in rat parotid acinar cells. Eur J Pharmacol. 1992 Mar 12;225(3):209–216. doi: 10.1016/0922-4106(92)90022-n. [DOI] [PubMed] [Google Scholar]
  20. Lee C., Fisher S. K., Agranoff B. W., Hajra A. K. Quantitative analysis of molecular species of diacylglycerol and phosphatidate formed upon muscarinic receptor activation of human SK-N-SH neuroblastoma cells. J Biol Chem. 1991 Dec 5;266(34):22837–22846. [PubMed] [Google Scholar]
  21. Maranto A. R. Primary structure, ligand binding, and localization of the human type 3 inositol 1,4,5-trisphosphate receptor expressed in intestinal epithelium. J Biol Chem. 1994 Jan 14;269(2):1222–1230. [PubMed] [Google Scholar]
  22. Messer M., Dahlqvist A. A one-step ultramicro method for the assay of intestinal disaccharidases. Anal Biochem. 1966 Mar;14(3):376–392. doi: 10.1016/0003-2697(66)90280-6. [DOI] [PubMed] [Google Scholar]
  23. Nakanishi O., Shibasaki F., Hidaka M., Homma Y., Takenawa T. Phospholipase C-gamma 1 associates with viral and cellular src kinases. J Biol Chem. 1993 May 25;268(15):10754–10759. [PubMed] [Google Scholar]
  24. Nathanson M. H., Fallon M. B., Padfield P. J., Maranto A. R. Localization of the type 3 inositol 1,4,5-trisphosphate receptor in the Ca2+ wave trigger zone of pancreatic acinar cells. J Biol Chem. 1994 Feb 18;269(7):4693–4696. [PubMed] [Google Scholar]
  25. Nishibe S., Wahl M. I., Hernández-Sotomayor S. M., Tonks N. K., Rhee S. G., Carpenter G. Increase of the catalytic activity of phospholipase C-gamma 1 by tyrosine phosphorylation. Science. 1990 Nov 30;250(4985):1253–1256. doi: 10.1126/science.1700866. [DOI] [PubMed] [Google Scholar]
  26. Reinlib L., Mikkelsen R., Zahniser D., Dharmsathaphorn K., Donowitz M. Carbachol-induced cytosolic free Ca2+ increases in T84 colonic cells seen by microfluorimetry. Am J Physiol. 1989 Dec;257(6 Pt 1):G950–G960. doi: 10.1152/ajpgi.1989.257.6.G950. [DOI] [PubMed] [Google Scholar]
  27. Ryu S. H., Kim U. H., Wahl M. I., Brown A. B., Carpenter G., Huang K. P., Rhee S. G. Feedback regulation of phospholipase C-beta by protein kinase C. J Biol Chem. 1990 Oct 15;265(29):17941–17945. [PubMed] [Google Scholar]
  28. Somogyi L., Lasić Z., Vukicević S., Banfić H. Collagen type IV stimulates an increase in intracellular Ca2+ in pancreatic acinar cells via activation of phospholipase C. Biochem J. 1994 May 1;299(Pt 3):603–611. doi: 10.1042/bj2990603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tapper E. J., Powell D. W., Morris S. M. Cholinergic-adrenergic interactions on intestinal ion transport. Am J Physiol. 1978 Oct;235(4):E402–E409. doi: 10.1152/ajpendo.1978.235.4.E402. [DOI] [PubMed] [Google Scholar]
  30. Thorn P., Lawrie A. M., Smith P. M., Gallacher D. V., Petersen O. H. Local and global cytosolic Ca2+ oscillations in exocrine cells evoked by agonists and inositol trisphosphate. Cell. 1993 Aug 27;74(4):661–668. doi: 10.1016/0092-8674(93)90513-p. [DOI] [PubMed] [Google Scholar]
  31. Vaandrager A. B., Ploemacher M. C., De Jonge H. R. Phosphoinositide metabolism in intestinal brush borders: stimulation of IP3 formation by guanine nucleotides and Ca2+. Am J Physiol. 1990 Sep;259(3 Pt 1):G410–G419. doi: 10.1152/ajpgi.1990.259.3.G410. [DOI] [PubMed] [Google Scholar]
  32. Weiser M. M. Intestinal epithelial cell surface membrane glycoprotein synthesis. I. An indicator of cellular differentiation. J Biol Chem. 1973 Apr 10;248(7):2536–2541. [PubMed] [Google Scholar]
  33. Wright T. M., Rangan L. A., Shin H. S., Raben D. M. Kinetic analysis of 1,2-diacylglycerol mass levels in cultured fibroblasts. Comparison of stimulation by alpha-thrombin and epidermal growth factor. J Biol Chem. 1988 Jul 5;263(19):9374–9380. [PubMed] [Google Scholar]
  34. Yang L., Camoratto A. M., Baffy G., Raj S., Manning D. R., Williamson J. R. Epidermal growth factor-mediated signaling of G(i)-protein to activation of phospholipases in rat-cultured hepatocytes. J Biol Chem. 1993 Feb 15;268(5):3739–3746. [PubMed] [Google Scholar]
  35. Zheng L., Stojilkovic S. S., Hunyady L., Krsmanovic L. Z., Catt K. J. Sequential activation of phospholipase-C and -D in agonist-stimulated gonadotrophs. Endocrinology. 1994 Mar;134(3):1446–1454. doi: 10.1210/endo.134.3.8119185. [DOI] [PubMed] [Google Scholar]

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