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British Journal of Cancer logoLink to British Journal of Cancer
. 1999 Jun;80(7):1012–1019. doi: 10.1038/sj.bjc.6690456

Amphiregulin acts as an autocrine growth factor in two human polarizing colon cancer lines that exhibit domain selective EGF receptor mitogenesis

L Damstrup 1,2, S K Kuwada 3,4, P J Dempsey 1, C L Brown 1, C J Hawkey 1, H S Poulsen 2, H S Wiley 3, R J Coffey Jr 1
PMCID: PMC2363033  PMID: 10362109

Abstract

Colonic enterocytes, like many epithelial cells in vivo, are polarized with functionally distinct apical and basolateral membrane domains. The aims of this study were to characterize the endogenous epidermal growth factor (EGF)-like ligands expressed in two polarizing colon cancer cell lines, HCA-7 Colony 29 (HCA-7) and Caco-2, and to examine the effects of cell polarity on EGF receptor-mediated mitogenesis. HCA-7 and Caco-2 cells were grown on plastic, or as a polarized monolayer on Transwell filters. Cell proliferation was measured by 3H-thymidine incorporation and EGF receptor (EGFR) binding was assessed by Scatchard analysis. EGFR ligand expression was determined by Northern blot analysis, reverse transcription polymerase chain reaction, metabolic labelling and confocal microscopy. We found that amphiregulin (AR) was the most abundant EGFR ligand expressed in HCA-7 and Caco-2 cells. AR was localized to the basolateral surface and detected in basolateral-conditioned medium. Basolateral administration of neutralizing AR antibodies significantly reduced basal DNA replication. A single class of high-affinity EGFRs was detected in the basolateral compartment, whereas the apical compartment of polarized cells, and cells cultured on plastic, displayed two classes of receptor affinity. Basolateral administration of transforming growth factor alpha (TGF-α) or an EGFR neutralizing antibody also resulted in a dose-dependent stimulation or attenuation, respectively, of DNA replication. However, no mitogenic response was observed when these agents were added to the apical compartment or to confluent cells cultured on plastic. We conclude that amphiregulin acts as an autocrine growth factor in HCA-7 and Caco-2 cells, and EGFR ligand-induced proliferation is influenced by cellular polarity. © 1999 Cancer Research Campaign

Keywords: EGFR, polarized cells, colon cancer cell lines, ligand and proliferation

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Selected References

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  1. Amemiya K., Kurachi H., Adachi H., Morishige K. I., Adachi K., Imai T., Miyake A. Involvement of epidermal growth factor (EGF)/EGF receptor autocrine and paracrine mechanism in human trophoblast cells: functional differentiation in vitro. J Endocrinol. 1994 Nov;143(2):291–301. doi: 10.1677/joe.0.1430291. [DOI] [PubMed] [Google Scholar]
  2. Auricchio A., di Domenico M., Castoria G., Bilancio A., Migliaccio A. Epidermal growth factor induces protein tyrosine phosphorylation and association of p190 with ras-GTP-ase activating protein in Caco-2 cells. FEBS Lett. 1994 Oct 10;353(1):16–20. doi: 10.1016/0014-5793(94)00987-2. [DOI] [PubMed] [Google Scholar]
  3. Bannykh S. I., Balch W. E. Membrane dynamics at the endoplasmic reticulum-Golgi interface. J Cell Biol. 1997 Jul 14;138(1):1–4. doi: 10.1083/jcb.138.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Basson M. D., Beidler D. R., Turowski G., Zarif A., Modlin I. M., Jena B. P., Madri J. A. Effect of tyrosine kinase inhibition on basal and epidermal growth factor-stimulated human Caco-2 enterocyte sheet migration and proliferation. J Cell Physiol. 1994 Sep;160(3):491–501. doi: 10.1002/jcp.1041600312. [DOI] [PubMed] [Google Scholar]
  5. Basson M. D., Modlin I. M., Madri J. A. Human enterocyte (Caco-2) migration is modulated in vitro by extracellular matrix composition and epidermal growth factor. J Clin Invest. 1992 Jul;90(1):15–23. doi: 10.1172/JCI115828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bellot F., Moolenaar W., Kris R., Mirakhur B., Verlaan I., Ullrich A., Schlessinger J., Felder S. High-affinity epidermal growth factor binding is specifically reduced by a monoclonal antibody, and appears necessary for early responses. J Cell Biol. 1990 Feb;110(2):491–502. doi: 10.1083/jcb.110.2.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bishop W. P., Wen J. T. Regulation of Caco-2 cell proliferation by basolateral membrane epidermal growth factor receptors. Am J Physiol. 1994 Nov;267(5 Pt 1):G892–G900. doi: 10.1152/ajpgi.1994.267.5.G892. [DOI] [PubMed] [Google Scholar]
  8. Brown C. L., Meise K. S., Plowman G. D., Coffey R. J., Dempsey P. J. Cell surface ectodomain cleavage of human amphiregulin precursor is sensitive to a metalloprotease inhibitor. Release of a predominant N-glycosylated 43-kDa soluble form. J Biol Chem. 1998 Jul 3;273(27):17258–17268. doi: 10.1074/jbc.273.27.17258. [DOI] [PubMed] [Google Scholar]
  9. Chen P., Gupta K., Wells A. Cell movement elicited by epidermal growth factor receptor requires kinase and autophosphorylation but is separable from mitogenesis. J Cell Biol. 1994 Feb;124(4):547–555. doi: 10.1083/jcb.124.4.547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Chinery R., Cox H. M. Modulation of epidermal growth factor effects on epithelial ion transport by intestinal trefoil factor. Br J Pharmacol. 1995 May;115(1):77–80. doi: 10.1111/j.1476-5381.1995.tb16322.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Coffey R. J., Hawkey C. J., Damstrup L., Graves-Deal R., Daniel V. C., Dempsey P. J., Chinery R., Kirkland S. C., DuBois R. N., Jetton T. L. Epidermal growth factor receptor activation induces nuclear targeting of cyclooxygenase-2, basolateral release of prostaglandins, and mitogenesis in polarizing colon cancer cells. Proc Natl Acad Sci U S A. 1997 Jan 21;94(2):657–662. doi: 10.1073/pnas.94.2.657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cook P. W., Pittelkow M. R., Keeble W. W., Graves-Deal R., Coffey R. J., Jr, Shipley G. D. Amphiregulin messenger RNA is elevated in psoriatic epidermis and gastrointestinal carcinomas. Cancer Res. 1992 Jun 1;52(11):3224–3227. [PubMed] [Google Scholar]
  13. Culouscou J. M., Remacle-Bonnet M., Carlton G. W., Plowman G. D., Shoyab M. Colorectum cell-derived growth factor (CRDGF) is homologous to amphiregulin, a member of the epidermal growth factor family. Growth Factors. 1992;7(3):195–205. doi: 10.3109/08977199209046924. [DOI] [PubMed] [Google Scholar]
  14. Danielson P. E., Forss-Petter S., Brow M. A., Calavetta L., Douglass J., Milner R. J., Sutcliffe J. G. p1B15: a cDNA clone of the rat mRNA encoding cyclophilin. DNA. 1988 May;7(4):261–267. doi: 10.1089/dna.1988.7.261. [DOI] [PubMed] [Google Scholar]
  15. Defize L. H., Boonstra J., Meisenhelder J., Kruijer W., Tertoolen L. G., Tilly B. C., Hunter T., van Bergen en Henegouwen P. M., Moolenaar W. H., de Laat S. W. Signal transduction by epidermal growth factor occurs through the subclass of high affinity receptors. J Cell Biol. 1989 Nov;109(5):2495–2507. doi: 10.1083/jcb.109.5.2495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Dempsey P. J., Coffey R. J. Basolateral targeting and efficient consumption of transforming growth factor-alpha when expressed in Madin-Darby canine kidney cells. J Biol Chem. 1994 Jun 17;269(24):16878–16889. [PubMed] [Google Scholar]
  17. Dobner P. R., Kawasaki E. S., Yu L. Y., Bancroft F. C. Thyroid or glucocorticoid hormone induces pre-growth-hormone mRNA and its probable nuclear precursor in rat pituitary cells. Proc Natl Acad Sci U S A. 1981 Apr;78(4):2230–2234. doi: 10.1073/pnas.78.4.2230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Feldman H. A. Mathematical theory of complex ligand-binding systems of equilibrium: some methods for parameter fitting. Anal Biochem. 1972 Aug;48(2):317–338. doi: 10.1016/0003-2697(72)90084-x. [DOI] [PubMed] [Google Scholar]
  19. Fowler K. J., Walker F., Alexander W., Hibbs M. L., Nice E. C., Bohmer R. M., Mann G. B., Thumwood C., Maglitto R., Danks J. A. A mutation in the epidermal growth factor receptor in waved-2 mice has a profound effect on receptor biochemistry that results in impaired lactation. Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1465–1469. doi: 10.1073/pnas.92.5.1465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Fuller S. D., Simons K. Transferrin receptor polarity and recycling accuracy in "tight" and "leaky" strains of Madin-Darby canine kidney cells. J Cell Biol. 1986 Nov;103(5):1767–1779. doi: 10.1083/jcb.103.5.1767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Gex-Fabry M., DeLisi C. Regulation of interacting populations during endocytosis: models of growth factor-tumor promoter dynamics. Am J Physiol. 1986 Jun;250(6 Pt 2):R1123–R1132. doi: 10.1152/ajpregu.1986.250.6.R1123. [DOI] [PubMed] [Google Scholar]
  22. Gilbert T., Le Bivic A., Quaroni A., Rodriguez-Boulan E. Microtubular organization and its involvement in the biogenetic pathways of plasma membrane proteins in Caco-2 intestinal epithelial cells. J Cell Biol. 1991 Apr;113(2):275–288. doi: 10.1083/jcb.113.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Halter S. A., Dempsey P., Matsui Y., Stokes M. K., Graves-Deal R., Hogan B. L., Coffey R. J. Distinctive patterns of hyperplasia in transgenic mice with mouse mammary tumor virus transforming growth factor-alpha. Characterization of mammary gland and skin proliferations. Am J Pathol. 1992 May;140(5):1131–1146. [PMC free article] [PubMed] [Google Scholar]
  24. Hobert M., Carlin C. Cytoplasmic juxtamembrane domain of the human EGF receptor is required for basolateral localization in MDCK cells. J Cell Physiol. 1995 Mar;162(3):434–446. doi: 10.1002/jcp.1041620316. [DOI] [PubMed] [Google Scholar]
  25. Johnson G. R., Saeki T., Gordon A. W., Shoyab M., Salomon D. S., Stromberg K. Autocrine action of amphiregulin in a colon carcinoma cell line and immunocytochemical localization of amphiregulin in human colon. J Cell Biol. 1992 Aug;118(3):741–751. doi: 10.1083/jcb.118.3.741. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Kirkland S. C. Dome formation by a human colonic adenocarcinoma cell line (HCA-7). Cancer Res. 1985 Aug;45(8):3790–3795. [PubMed] [Google Scholar]
  27. Li S., Plowman G. D., Buckley S. D., Shipley G. D. Heparin inhibition of autonomous growth implicates amphiregulin as an autocrine growth factor for normal human mammary epithelial cells. J Cell Physiol. 1992 Oct;153(1):103–111. doi: 10.1002/jcp.1041530114. [DOI] [PubMed] [Google Scholar]
  28. Luetteke N. C., Phillips H. K., Qiu T. H., Copeland N. G., Earp H. S., Jenkins N. A., Lee D. C. The mouse waved-2 phenotype results from a point mutation in the EGF receptor tyrosine kinase. Genes Dev. 1994 Feb 15;8(4):399–413. doi: 10.1101/gad.8.4.399. [DOI] [PubMed] [Google Scholar]
  29. Maratos-Flier E., Kao C. Y., Verdin E. M., King G. L. Receptor-mediated vectorial transcytosis of epidermal growth factor by Madin-Darby canine kidney cells. J Cell Biol. 1987 Oct;105(4):1595–1601. doi: 10.1083/jcb.105.4.1595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Martinez-Palomo A., Meza I., Beaty G., Cereijido M. Experimental modulation of occluding junctions in a cultured transporting epithelium. J Cell Biol. 1980 Dec;87(3 Pt 1):736–745. doi: 10.1083/jcb.87.3.736. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Mayo K. H., Nunez M., Burke C., Starbuck C., Lauffenburger D., Savage C. R., Jr Epidermal growth factor receptor binding is not a simple one-step process. J Biol Chem. 1989 Oct 25;264(30):17838–17844. [PubMed] [Google Scholar]
  32. Melton D. A., Krieg P. A., Rebagliati M. R., Maniatis T., Zinn K., Green M. R. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 1984 Sep 25;12(18):7035–7056. doi: 10.1093/nar/12.18.7035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Milovic V., Deubner C., Zeuzem S., Piiper A., Caspary W. F., Stein J. EGF stimulates polyamine uptake in Caco-2 cells. Biochem Biophys Res Commun. 1995 Jan 26;206(3):962–968. doi: 10.1006/bbrc.1995.1136. [DOI] [PubMed] [Google Scholar]
  34. Pesonen M., Simons K. Transepithelial transport of a viral membrane glycoprotein implanted into the apical plasma membrane of Madin-Darby canine kidney cells. II. Immunological quantitation. J Cell Biol. 1983 Sep;97(3):638–643. doi: 10.1083/jcb.97.3.638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Qi C. F., Liscia D. S., Normanno N., Merlo G., Johnson G. R., Gullick W. J., Ciardiello F., Saeki T., Brandt R., Kim N. Expression of transforming growth factor alpha, amphiregulin and cripto-1 in human breast carcinomas. Br J Cancer. 1994 May;69(5):903–910. doi: 10.1038/bjc.1994.174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Traverse S., Seedorf K., Paterson H., Marshall C. J., Cohen P., Ullrich A. EGF triggers neuronal differentiation of PC12 cells that overexpress the EGF receptor. Curr Biol. 1994 Aug 1;4(8):694–701. doi: 10.1016/s0960-9822(00)00154-8. [DOI] [PubMed] [Google Scholar]
  37. Wofsy C., Goldstein B., Lund K., Wiley H. S. Implications of epidermal growth factor (EGF) induced egf receptor aggregation. Biophys J. 1992 Jul;63(1):98–110. doi: 10.1016/S0006-3495(92)81572-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Ziober B. L., Willson J. K., Hymphrey L. E., Childress-Fields K., Brattain M. G. Autocrine transforming growth factor-alpha is associated with progression of transformed properties in human colon cancer cells. J Biol Chem. 1993 Jan 5;268(1):691–698. [PubMed] [Google Scholar]

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