Abstract
In simple epithelia, the distribution of ion transporting proteins between the apical or basal-lateral domains of the plasma membrane is important for determining directions of vectorial ion transport across the epithelium. In the choroid plexus, Na+,K(+)-ATPase is localized to the apical plasma membrane domain where it regulates sodium secretion and production of cerebrospinal fluid; in contrast, Na+,K(+)-ATPase is localized to the basal-lateral membrane of cells in the kidney nephron where it regulates ion and solute reabsorption. The mechanisms involved in restricting Na+,K(+)-ATPase distribution to different membrane domains in these simple epithelia are poorly understood. Previous studies have indicated a role for E-cadherin mediated cell-cell adhesion and membrane-cytoskeleton (ankyrin and fodrin) assembly in regulating Na+,K(+)-ATPase distribution in absorptive kidney epithelial cells. Confocal immunofluorescence microscopy reveals that in chicken and rat choroid plexus epithelium, fodrin, and ankyrin colocalize with Na+,K(+)-ATPase at the apical plasma membrane, but fodrin, ankyrin, and adducin also localize at the lateral plasma membrane where Na+,K(+)- ATPase is absent. Biochemical analysis shows that fodrin, ankyrin, and Na+,K(+)-ATPase are relatively resistant to extraction from cells in buffers containing Triton X-100. The fractions of Na+,K(+)-ATPase, fodrin, and ankyrin that are extracted from cells cosediment in sucrose gradients at approximately 10.5 S. Further separation of the 10.5 S peak of proteins by electrophoresis in nondenaturing polyacrylamide gels revealed that fodrin, ankyrin, and Na+,K(+)-ATPase comigrate, indicating that these proteins are in a high molecular weight complex similar to that found previously in kidney epithelial cells. In contrast, the anion exchanger (AE2), a marker protein of the basal- lateral plasma membrane in the choroid plexus, did not cosediment in sucrose gradients or comigrate in nondenaturing polyacrylamide gels with the complex of Na+,K(+)-ATPase, ankyrin, and fodrin. Ca(++)- dependent cell adhesion molecules (cadherins) were detected at lateral membranes of the choroid plexus epithelium and colocalized with a distinct fraction of ankyrin, fodrin, and adducin. Cadherins did not colocalize with Na+,K(+)-ATPase and were absent from the apical membrane. The fraction of cadherins that was extracted with buffers containing Triton X-100 cosedimented with ankyrin and fodrin in sucrose gradients and comigrated in nondenaturing gels with ankyrin and fodrin in a high molecular weight complex. Since a previous study showed that E-cadherin is an instructive inducer of Na+,K(+)-ATPase distribution, we examined protein distributions in fibroblasts transfected with B- cadherin, a prominent cadherin expressed in the choroid plexus epithelium.(ABSTRACT TRUNCATED AT 400 WORDS)
Full Text
The Full Text of this article is available as a PDF (5.4 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Almers W., Stirling C. Distribution of transport proteins over animal cell membranes. J Membr Biol. 1984;77(3):169–186. doi: 10.1007/BF01870567. [DOI] [PubMed] [Google Scholar]
- Avner E. D., Sweeney W. E., Jr, Nelson W. J. Abnormal sodium pump distribution during renal tubulogenesis in congenital murine polycystic kidney disease. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7447–7451. doi: 10.1073/pnas.89.16.7447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennett V., Gardner K., Steiner J. P. Brain adducin: a protein kinase C substrate that may mediate site-directed assembly at the spectrin-actin junction. J Biol Chem. 1988 Apr 25;263(12):5860–5869. [PubMed] [Google Scholar]
- Bennett V. Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasm. Physiol Rev. 1990 Oct;70(4):1029–1065. doi: 10.1152/physrev.1990.70.4.1029. [DOI] [PubMed] [Google Scholar]
- Bennett V., Stenbuck P. J. Human erythrocyte ankyrin. Purification and properties. J Biol Chem. 1980 Mar 25;255(6):2540–2548. [PubMed] [Google Scholar]
- Boller K., Vestweber D., Kemler R. Cell-adhesion molecule uvomorulin is localized in the intermediate junctions of adult intestinal epithelial cells. J Cell Biol. 1985 Jan;100(1):327–332. doi: 10.1083/jcb.100.1.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coleman T. R., Fishkind D. J., Mooseker M. S., Morrow J. S. Contributions of the beta-subunit to spectrin structure and function. Cell Motil Cytoskeleton. 1989;12(4):248–263. doi: 10.1002/cm.970120406. [DOI] [PubMed] [Google Scholar]
- Davis J. Q., Bennett V. The anion exchanger and Na+K(+)-ATPase interact with distinct sites on ankyrin in in vitro assays. J Biol Chem. 1990 Oct 5;265(28):17252–17256. [PubMed] [Google Scholar]
- Ernst S. A., Palacios J. R., 2nd, Siegel G. J. Immunocytochemical localization of Na+,K+-ATPase catalytic polypeptide in mouse choroid plexus. J Histochem Cytochem. 1986 Feb;34(2):189–195. doi: 10.1177/34.2.3003182. [DOI] [PubMed] [Google Scholar]
- Gardner K., Bennett V. Modulation of spectrin-actin assembly by erythrocyte adducin. Nature. 1987 Jul 23;328(6128):359–362. doi: 10.1038/328359a0. [DOI] [PubMed] [Google Scholar]
- Geiger B., Ayalon O. Cadherins. Annu Rev Cell Biol. 1992;8:307–332. doi: 10.1146/annurev.cb.08.110192.001515. [DOI] [PubMed] [Google Scholar]
- Ghosh S., Freitag A. C., Martin-Vasallo P., Coca-Prados M. Cellular distribution and differential gene expression of the three alpha subunit isoforms of the Na,K-ATPase in the ocular ciliary epithelium. J Biol Chem. 1990 Feb 15;265(5):2935–2940. [PubMed] [Google Scholar]
- Gottardi C. J., Caplan M. J. Delivery of Na+,K(+)-ATPase in polarized epithelial cells. Science. 1993 Apr 23;260(5107):552–556. doi: 10.1126/science.8386395. [DOI] [PubMed] [Google Scholar]
- Gundersen D., Orlowski J., Rodriguez-Boulan E. Apical polarity of Na,K-ATPase in retinal pigment epithelium is linked to a reversal of the ankyrin-fodrin submembrane cytoskeleton. J Cell Biol. 1991 Mar;112(5):863–872. doi: 10.1083/jcb.112.5.863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gundersen D., Powell S. K., Rodriguez-Boulan E. Apical polarization of N-CAM in retinal pigment epithelium is dependent on contact with the neural retina. J Cell Biol. 1993 Apr;121(2):335–343. doi: 10.1083/jcb.121.2.335. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hammerton R. W., Krzeminski K. A., Mays R. W., Ryan T. A., Wollner D. A., Nelson W. J. Mechanism for regulating cell surface distribution of Na+,K(+)-ATPase in polarized epithelial cells. Science. 1991 Nov 8;254(5033):847–850. doi: 10.1126/science.1658934. [DOI] [PubMed] [Google Scholar]
- Hargreaves W. R., Giedd K. N., Verkleij A., Branton D. Reassociation of ankyrin with band 3 in erythrocyte membranes and in lipid vesicles. J Biol Chem. 1980 Dec 25;255(24):11965–11972. [PubMed] [Google Scholar]
- Kaiser H. W., O'Keefe E., Bennett V. Adducin: Ca++-dependent association with sites of cell-cell contact. J Cell Biol. 1989 Aug;109(2):557–569. doi: 10.1083/jcb.109.2.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kemler R. Classical cadherins. Semin Cell Biol. 1992 Jun;3(3):149–155. doi: 10.1016/s1043-4682(10)80011-x. [DOI] [PubMed] [Google Scholar]
- Koob R., Zimmermann M., Schoner W., Drenckhahn D. Colocalization and coprecipitation of ankyrin and Na+,K+-ATPase in kidney epithelial cells. Eur J Cell Biol. 1988 Feb;45(2):230–237. [PubMed] [Google Scholar]
- Kopito R. R. Molecular biology of the anion exchanger gene family. Int Rev Cytol. 1990;123:177–199. doi: 10.1016/s0074-7696(08)60674-9. [DOI] [PubMed] [Google Scholar]
- Kudrycki K. E., Newman P. R., Shull G. E. cDNA cloning and tissue distribution of mRNAs for two proteins that are related to the band 3 Cl-/HCO3- exchanger. J Biol Chem. 1990 Jan 5;265(1):462–471. [PubMed] [Google Scholar]
- Lindsey A. E., Schneider K., Simmons D. M., Baron R., Lee B. S., Kopito R. R. Functional expression and subcellular localization of an anion exchanger cloned from choroid plexus. Proc Natl Acad Sci U S A. 1990 Jul;87(14):5278–5282. doi: 10.1073/pnas.87.14.5278. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Masuzawa T., Ohta T., Kawakami K., Sato F. Immunocytochemical localization of Na+, K+-ATPase in the canine choroid plexus. Brain. 1985 Sep;108(Pt 3):625–646. doi: 10.1093/brain/108.3.625. [DOI] [PubMed] [Google Scholar]
- Masuzawa T., Ohta T., Kawamura M., Nakahara N., Sato F. Immunohistochemical localization of Na+, K+-ATPase in the choroid plexus. Brain Res. 1984 Jun 8;302(2):357–362. doi: 10.1016/0006-8993(84)90250-6. [DOI] [PubMed] [Google Scholar]
- McNeill H., Ozawa M., Kemler R., Nelson W. J. Novel function of the cell adhesion molecule uvomorulin as an inducer of cell surface polarity. Cell. 1990 Jul 27;62(2):309–316. doi: 10.1016/0092-8674(90)90368-o. [DOI] [PubMed] [Google Scholar]
- Minuth W. W., Gross P., Gilbert P., Kashgarian M. Expression of the alpha-subunit of Na/K-ATPase in renal collecting duct epithelium during development. Kidney Int. 1987 May;31(5):1104–1112. doi: 10.1038/ki.1987.115. [DOI] [PubMed] [Google Scholar]
- Mische S. M., Mooseker M. S., Morrow J. S. Erythrocyte adducin: a calmodulin-regulated actin-bundling protein that stimulates spectrin-actin binding. J Cell Biol. 1987 Dec;105(6 Pt 1):2837–2845. doi: 10.1083/jcb.105.6.2837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Molitoris B. A. New insights into the cell biology of ischemic acute renal failure. J Am Soc Nephrol. 1991 Jun;1(12):1263–1270. doi: 10.1681/ASN.V1121263. [DOI] [PubMed] [Google Scholar]
- Morrow J. S., Cianci C. D., Ardito T., Mann A. S., Kashgarian M. Ankyrin links fodrin to the alpha subunit of Na,K-ATPase in Madin-Darby canine kidney cells and in intact renal tubule cells. J Cell Biol. 1989 Feb;108(2):455–465. doi: 10.1083/jcb.108.2.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mostov K., Apodaca G., Aroeti B., Okamoto C. Plasma membrane protein sorting in polarized epithelial cells. J Cell Biol. 1992 Feb;116(3):577–583. doi: 10.1083/jcb.116.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nagafuchi A., Takeichi M. Transmembrane control of cadherin-mediated cell adhesion: a 94 kDa protein functionally associated with a specific region of the cytoplasmic domain of E-cadherin. Cell Regul. 1989 Nov;1(1):37–44. doi: 10.1091/mbc.1.1.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Napolitano E. W., Venstrom K., Wheeler E. F., Reichardt L. F. Molecular cloning and characterization of B-cadherin, a novel chick cadherin. J Cell Biol. 1991 May;113(4):893–905. doi: 10.1083/jcb.113.4.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nelson W. J., Hammerton R. W. A membrane-cytoskeletal complex containing Na+,K+-ATPase, ankyrin, and fodrin in Madin-Darby canine kidney (MDCK) cells: implications for the biogenesis of epithelial cell polarity. J Cell Biol. 1989 Mar;108(3):893–902. doi: 10.1083/jcb.108.3.893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nelson W. J., Hammerton R. W., Wang A. Z., Shore E. M. Involvement of the membrane-cytoskeleton in development of epithelial cell polarity. Semin Cell Biol. 1990 Oct;1(5):359–371. [PubMed] [Google Scholar]
- Nelson W. J. Regulation of cell surface polarity from bacteria to mammals. Science. 1992 Nov 6;258(5084):948–955. doi: 10.1126/science.1439806. [DOI] [PubMed] [Google Scholar]
- Nelson W. J., Shore E. M., Wang A. Z., Hammerton R. W. Identification of a membrane-cytoskeletal complex containing the cell adhesion molecule uvomorulin (E-cadherin), ankyrin, and fodrin in Madin-Darby canine kidney epithelial cells. J Cell Biol. 1990 Feb;110(2):349–357. doi: 10.1083/jcb.110.2.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nelson W. J., Veshnock P. J. Ankyrin binding to (Na+ + K+)ATPase and implications for the organization of membrane domains in polarized cells. Nature. 1987 Aug 6;328(6130):533–536. doi: 10.1038/328533a0. [DOI] [PubMed] [Google Scholar]
- Nelson W. J., Veshnock P. J. Dynamics of membrane-skeleton (fodrin) organization during development of polarity in Madin-Darby canine kidney epithelial cells. J Cell Biol. 1986 Nov;103(5):1751–1765. doi: 10.1083/jcb.103.5.1751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nelson W. J., Veshnock P. J. Modulation of fodrin (membrane skeleton) stability by cell-cell contact in Madin-Darby canine kidney epithelial cells. J Cell Biol. 1987 Jun;104(6):1527–1537. doi: 10.1083/jcb.104.6.1527. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozawa M., Baribault H., Kemler R. The cytoplasmic domain of the cell adhesion molecule uvomorulin associates with three independent proteins structurally related in different species. EMBO J. 1989 Jun;8(6):1711–1717. doi: 10.1002/j.1460-2075.1989.tb03563.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ringwald M., Baribault H., Schmidt C., Kemler R. The structure of the gene coding for the mouse cell adhesion molecule uvomorulin. Nucleic Acids Res. 1991 Dec 11;19(23):6533–6539. doi: 10.1093/nar/19.23.6533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodriguez-Boulan E., Powell S. K. Polarity of epithelial and neuronal cells. Annu Rev Cell Biol. 1992;8:395–427. doi: 10.1146/annurev.cb.08.110192.002143. [DOI] [PubMed] [Google Scholar]
- Shore E. M., Nelson W. J. Biosynthesis of the cell adhesion molecule uvomorulin (E-cadherin) in Madin-Darby canine kidney epithelial cells. J Biol Chem. 1991 Oct 15;266(29):19672–19680. [PubMed] [Google Scholar]
- Siegel G. J., Holm C., Schreiber J. H., Desmond T., Ernst S. A. Purification of mouse brain (Na+ + K+)-ATPase catalytic unit, characterization of antiserum, and immunocytochemical localization in cerebellum, choroid plexus, and kidney. J Histochem Cytochem. 1984 Dec;32(12):1309–1318. doi: 10.1177/32.12.6094658. [DOI] [PubMed] [Google Scholar]
- Siemers Krzeminski K. A., Wilson Hammerton R., Mays R. W., Ryan T. A., Wollner D. A., Nelson W. J. Response. Science. 1993 Apr 23;260(5107):554–556. doi: 10.1126/science.260.5107.554. [DOI] [PubMed] [Google Scholar]
- Sorkin B. C., Gallin W. J., Edelman G. M., Cunningham B. A. Genes for two calcium-dependent cell adhesion molecules have similar structures and are arranged in tandem in the chicken genome. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11545–11549. doi: 10.1073/pnas.88.24.11545. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spector R., Johanson C. E. The mammalian choroid plexus. Sci Am. 1989 Nov;261(5):68–74. doi: 10.1038/scientificamerican1189-68. [DOI] [PubMed] [Google Scholar]
- Sweadner K. J. Isozymes of the Na+/K+-ATPase. Biochim Biophys Acta. 1989 May 9;988(2):185–220. doi: 10.1016/0304-4157(89)90019-1. [DOI] [PubMed] [Google Scholar]
- Tyler J. M., Reinhardt B. N., Branton D. Associations of erythrocyte membrane proteins. Binding of purified bands 2.1 and 4.1 to spectrin. J Biol Chem. 1980 Jul 25;255(14):7034–7039. [PubMed] [Google Scholar]
- Watts A. G., Sanchez-Watts G., Emanuel J. R., Levenson R. Cell-specific expression of mRNAs encoding Na+,K(+)-ATPase alpha- and beta-subunit isoforms within the rat central nervous system. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7425–7429. doi: 10.1073/pnas.88.16.7425. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilson P. D., Sherwood A. C., Palla K., Du J., Watson R., Norman J. T. Reversed polarity of Na(+) -K(+) -ATPase: mislocation to apical plasma membranes in polycystic kidney disease epithelia. Am J Physiol. 1991 Mar;260(3 Pt 2):F420–F430. doi: 10.1152/ajprenal.1991.260.3.F420. [DOI] [PubMed] [Google Scholar]
- Wright E. M. Mechanisms of ion transport across the choroid plexus. J Physiol. 1972 Oct;226(2):545–571. doi: 10.1113/jphysiol.1972.sp009997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zurzolo C., Rodriguez-Boulan E. Delivery of Na+,K(+)-ATPase in polarized epithelial cells. Science. 1993 Apr 23;260(5107):550–556. doi: 10.1126/science.8386394. [DOI] [PubMed] [Google Scholar]