Abstract
Gastric surface mucous cells originate from progenitor cells at the isthmus of the gastric gland, from where the cells migrate to the luminal surface. With migration they form secretory granules and express TGF alpha. We found that proprotein-processing endoprotease furin-positive cells were layered around the upper one fourth of the gastric glands of adult rats, whereas they were distributed along an outer epithelial layer in fetal rats. Because the furin-positive cell layer was localized from the upper cell proliferating zone to the less proliferating pit-cell region in the gastric gland unit, we examined the role of furin in the growth and differentiation of surface mucous cells by using the cell line, GSM06. This cell line is derived from the gastric surface mucous cells of transgenic mice harboring the temperature-sensitive simian virus 40 T antigen. At T antigen-active temperature (33 degrees C), the cells grew to confluency, whereas at T antigen-inactive temperature (39 degrees C), the cells ceased growing. At 33 degrees C, the cells exhibited a high level of furin expression with a negligible level of periodic acid Schiff (PAS)-positive materials and a low level of TGF alpha. In contrast, at 39 degrees C the cells produced a high level of PAS-positive materials, TGF alpha, and secretory granules, with a negligible level of furin expression. To further examine the role of furin, we established a GSM06 cell line introduced with either a sense or an antisense furin cDNA. The cells with sense furin expression produced fewer PAS-positive materials and a low level of TGF alpha even at 39 degrees C, whereas the cells with antisense furin expression exhibited more PAS-positive materials and TGF alpha even at 33 degrees C. When furin expression was suppressed by its antisense oligonucleotide, the cell growth was retarded with enhanced expression of the differentiated characteristics. Thus, we conclude that furin is instrumental in controlling the growth of the surface mucous cells.
Full Text
The Full Text of this article is available as a PDF (535.3 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allen A., Flemström G., Garner A., Kivilaakso E. Gastroduodenal mucosal protection. Physiol Rev. 1993 Oct;73(4):823–857. doi: 10.1152/physrev.1993.73.4.823. [DOI] [PubMed] [Google Scholar]
- Beauchamp R. D., Barnard J. A., McCutchen C. M., Cherner J. A., Coffey R. J., Jr Localization of transforming growth factor alpha and its receptor in gastric mucosal cells. Implications for a regulatory role in acid secretion and mucosal renewal. J Clin Invest. 1989 Sep;84(3):1017–1023. doi: 10.1172/JCI114223. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boland C. R., Kraus E. R., Scheiman J. M., Black C., Deshmukh G. D., Dobbins W. O., 3rd Characterization of mucous cell synthetic functions in a new primary canine gastric mucous cell culture system. Am J Physiol. 1990 May;258(5 Pt 1):G774–G787. doi: 10.1152/ajpgi.1990.258.5.G774. [DOI] [PubMed] [Google Scholar]
- Bravo D. A., Gleason J. B., Sanchez R. I., Roth R. A., Fuller R. S. Accurate and efficient cleavage of the human insulin proreceptor by the human proprotein-processing protease furin. Characterization and kinetic parameters using the purified, secreted soluble protease expressed by a recombinant baculovirus. J Biol Chem. 1994 Oct 14;269(41):25830–25837. [PubMed] [Google Scholar]
- Bresnahan P. A., Leduc R., Thomas L., Thorner J., Gibson H. L., Brake A. J., Barr P. J., Thomas G. Human fur gene encodes a yeast KEX2-like endoprotease that cleaves pro-beta-NGF in vivo. J Cell Biol. 1990 Dec;111(6 Pt 2):2851–2859. doi: 10.1083/jcb.111.6.2851. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen M. C., Lee A. T., Karnes W. E., Avedian D., Martin M., Sorvillo J. M., Soll A. H. Paracrine control of gastric epithelial cell growth in culture by transforming growth factor-alpha. Am J Physiol. 1993 Feb;264(2 Pt 1):G390–G396. doi: 10.1152/ajpgi.1993.264.2.G390. [DOI] [PubMed] [Google Scholar]
- Chen M. C., Lee A. T., Soll A. H. Mitogenic response of canine fundic epithelial cells in short-term culture to transforming growth factor alpha and insulinlike growth factor I. J Clin Invest. 1991 May;87(5):1716–1723. doi: 10.1172/JCI115189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dempsey P. J., Goldenring J. R., Soroka C. J., Modlin I. M., McClure R. W., Lind C. D., Ahlquist D. A., Pittelkow M. R., Lee D. C., Sandgren E. P. Possible role of transforming growth factor alpha in the pathogenesis of Ménétrier's disease: supportive evidence form humans and transgenic mice. Gastroenterology. 1992 Dec;103(6):1950–1963. doi: 10.1016/0016-5085(92)91455-d. [DOI] [PubMed] [Google Scholar]
- Derynck R., Roberts A. B., Winkler M. E., Chen E. Y., Goeddel D. V. Human transforming growth factor-alpha: precursor structure and expression in E. coli. Cell. 1984 Aug;38(1):287–297. doi: 10.1016/0092-8674(84)90550-6. [DOI] [PubMed] [Google Scholar]
- Dohi T., Nakasuji M., Nakanishi K., Yasugi E., Yuyama Y., Sugiyama N., Tabuchi Y., Horiuchi T., Oshima M. Biochemical bases in differentiation of a mouse cell line GSM06 to gastric surface cells. Biochim Biophys Acta. 1996 Feb 9;1289(1):71–78. doi: 10.1016/0304-4165(95)00138-7. [DOI] [PubMed] [Google Scholar]
- Dubois C. M., Laprise M. H., Blanchette F., Gentry L. E., Leduc R. Processing of transforming growth factor beta 1 precursor by human furin convertase. J Biol Chem. 1995 May 5;270(18):10618–10624. doi: 10.1074/jbc.270.18.10618. [DOI] [PubMed] [Google Scholar]
- Frederiksen K., Jat P. S., Valtz N., Levy D., McKay R. Immortalization of precursor cells from the mammalian CNS. Neuron. 1988 Aug;1(6):439–448. doi: 10.1016/0896-6273(88)90175-4. [DOI] [PubMed] [Google Scholar]
- Fukamachi H., Ichinose M., Ishihama S., Tsukada S., Yasugi S., Shiokawa K., Furihata C., Yonezawa S., Miki K. Fetal rat glandular stomach epithelial cells differentiate into surface mucous cells which express cathepsin E in the absence of mesenchymal cells in primary culture. Differentiation. 1994 Apr;56(1-2):83–89. doi: 10.1046/j.1432-0436.1994.56120083.x. [DOI] [PubMed] [Google Scholar]
- Goddard P. J., Kao Y. C., Lichtenberger L. M. Luminal surface hydrophobicity of canine gastric mucosa is dependent on a surface mucous gel. Gastroenterology. 1990 Feb;98(2):361–370. doi: 10.1016/0016-5085(90)90826-m. [DOI] [PubMed] [Google Scholar]
- Hatsuzawa K., Hosaka M., Nakagawa T., Nagase M., Shoda A., Murakami K., Nakayama K. Structure and expression of mouse furin, a yeast Kex2-related protease. Lack of processing of coexpressed prorenin in GH4C1 cells. J Biol Chem. 1990 Dec 25;265(36):22075–22078. [PubMed] [Google Scholar]
- Hatta K., Nose A., Nagafuchi A., Takeichi M. Cloning and expression of cDNA encoding a neural calcium-dependent cell adhesion molecule: its identity in the cadherin gene family. J Cell Biol. 1988 Mar;106(3):873–881. doi: 10.1083/jcb.106.3.873. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Helander H. F. Ultrastructure and function of gastric mucoid and zymogen cells in the rat during development. Gastroenterology. 1969 Jan;56(1):53–70. [PubMed] [Google Scholar]
- Helander H. F. Ultrastructure and function of gastric parietal cells in the rat during development. Gastroenterology. 1969 Jan;56(1):35–52. [PubMed] [Google Scholar]
- Hormi K., Onolfo J. P., Gres L., Lebraud V., Lehy T. Developmental expression of transforming growth factor-alpha in the upper digestive tract and pancreas of the rat. Regul Pept. 1995 Jan 5;55(1):67–77. doi: 10.1016/0167-0115(94)00093-d. [DOI] [PubMed] [Google Scholar]
- Jat P. S., Noble M. D., Ataliotis P., Tanaka Y., Yannoutsos N., Larsen L., Kioussis D. Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5096–5100. doi: 10.1073/pnas.88.12.5096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson L. R. Functional development of the stomach. Annu Rev Physiol. 1985;47:199–215. doi: 10.1146/annurev.ph.47.030185.001215. [DOI] [PubMed] [Google Scholar]
- Johnson L. R. Regulation of gastrointestinal mucosal growth. Physiol Rev. 1988 Apr;68(2):456–502. doi: 10.1152/physrev.1988.68.2.456. [DOI] [PubMed] [Google Scholar]
- Karam S. M., Leblond C. P. Dynamics of epithelial cells in the corpus of the mouse stomach. I. Identification of proliferative cell types and pinpointing of the stem cell. Anat Rec. 1993 Jun;236(2):259–279. doi: 10.1002/ar.1092360202. [DOI] [PubMed] [Google Scholar]
- Karam S. M., Leblond C. P. Dynamics of epithelial cells in the corpus of the mouse stomach. II. Outward migration of pit cells. Anat Rec. 1993 Jun;236(2):280–296. doi: 10.1002/ar.1092360203. [DOI] [PubMed] [Google Scholar]
- Kayo T., Konda Y., Tanaka S., Takata K., Koizumi A., Takeuchi T. Developmental expression of proprotein-processing endoprotease furin in rat pancreatic islets. Endocrinology. 1996 Nov;137(11):5126–5134. doi: 10.1210/endo.137.11.8895387. [DOI] [PubMed] [Google Scholar]
- Kayo T., Sawada Y., Suzuki Y., Suda M., Tanaka S., Konda Y., Miyazaki J., Takeuchi T. Proprotein-processing endoprotease furin decreases regulated secretory pathway-specific proteins in the pancreatic beta cell line MIN6. J Biol Chem. 1996 May 3;271(18):10731–10737. doi: 10.1074/jbc.271.18.10731. [DOI] [PubMed] [Google Scholar]
- Kelly S. M., Hunter J. O. Epidermal growth factor stimulates synthesis and secretion of mucus glycoproteins in human gastric mucosa. Clin Sci (Lond) 1990 Nov;79(5):425–427. doi: 10.1042/cs0790425. [DOI] [PubMed] [Google Scholar]
- Komada M., Hatsuzawa K., Shibamoto S., Ito F., Nakayama K., Kitamura N. Proteolytic processing of the hepatocyte growth factor/scatter factor receptor by furin. FEBS Lett. 1993 Aug 9;328(1-2):25–29. doi: 10.1016/0014-5793(93)80958-w. [DOI] [PubMed] [Google Scholar]
- Marchand P., Tang J., Johnson G. D., Bond J. S. COOH-terminal proteolytic processing of secreted and membrane forms of the alpha subunit of the metalloprotease meprin A. Requirement of the I domain for processing in the endoplasmic reticulum. J Biol Chem. 1995 Mar 10;270(10):5449–5456. doi: 10.1074/jbc.270.10.5449. [DOI] [PubMed] [Google Scholar]
- Matuoka K., Tanaka M., Mitsui Y., Murota S. I. Cultured rabbit gastric epithelial cells producing prostaglandin I2. Gastroenterology. 1983 Mar;84(3):498–505. [PubMed] [Google Scholar]
- Molloy S. S., Thomas L., VanSlyke J. K., Stenberg P. E., Thomas G. Intracellular trafficking and activation of the furin proprotein convertase: localization to the TGN and recycling from the cell surface. EMBO J. 1994 Jan 1;13(1):18–33. doi: 10.1002/j.1460-2075.1994.tb06231.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murayama Y., Miyagawa J., Higashiyama S., Kondo S., Yabu M., Isozaki K., Kayanoki Y., Kanayama S., Shinomura Y., Taniguchi N. Localization of heparin-binding epidermal growth factor-like growth factor in human gastric mucosa. Gastroenterology. 1995 Oct;109(4):1051–1059. doi: 10.1016/0016-5085(95)90562-6. [DOI] [PubMed] [Google Scholar]
- Nasim M. M., Thomas D. M., Alison M. R., Filipe M. I. Transforming growth factor alpha expression in normal gastric mucosa, intestinal metaplasia, dysplasia and gastric carcinoma--an immunohistochemical study. Histopathology. 1992 Apr;20(4):339–343. doi: 10.1111/j.1365-2559.1992.tb00991.x. [DOI] [PubMed] [Google Scholar]
- Pandiella A., Massagué J. Cleavage of the membrane precursor for transforming growth factor alpha is a regulated process. Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1726–1730. doi: 10.1073/pnas.88.5.1726. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pei D., Weiss S. J. Furin-dependent intracellular activation of the human stromelysin-3 zymogen. Nature. 1995 May 18;375(6528):244–247. doi: 10.1038/375244a0. [DOI] [PubMed] [Google Scholar]
- Rutten M. J., Dempsey P. J., Luttropp C. A., Hawkey M. A., Sheppard B. C., Crass R. A., Deveney C. W., Coffey R. J., Jr Identification of an EGF/TGF-alpha receptor in primary cultures of guinea pig gastric mucous epithelial cells. Am J Physiol. 1996 Apr;270(4 Pt 1):G604–G612. doi: 10.1152/ajpgi.1996.270.4.G604. [DOI] [PubMed] [Google Scholar]
- Sato H., Takino T., Okada Y., Cao J., Shinagawa A., Yamamoto E., Seiki M. A matrix metalloproteinase expressed on the surface of invasive tumour cells. Nature. 1994 Jul 7;370(6484):61–65. doi: 10.1038/370061a0. [DOI] [PubMed] [Google Scholar]
- Sharp R., Babyatsky M. W., Takagi H., Tågerud S., Wang T. C., Bockman D. E., Brand S. J., Merlino G. Transforming growth factor alpha disrupts the normal program of cellular differentiation in the gastric mucosa of transgenic mice. Development. 1995 Jan;121(1):149–161. doi: 10.1242/dev.121.1.149. [DOI] [PubMed] [Google Scholar]
- Soll A. H., Amirian D. A., Thomas L. P., Reedy T. J., Elashoff J. D. Gastrin receptors on isolated canine parietal cells. J Clin Invest. 1984 May;73(5):1434–1447. doi: 10.1172/JCI111348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sottili M., Sternini C., Brecha N. C., Lezoche E., Walsh J. H. Transforming growth factor alpha receptor binding sites in the canine gastrointestinal tract. Gastroenterology. 1992 Nov;103(5):1427–1436. doi: 10.1016/0016-5085(92)91161-v. [DOI] [PubMed] [Google Scholar]
- Sugiyama N., Tabuchi Y., Horiuchi T., Obinata M., Furusawa M. Establishment of gastric surface mucous cell lines from transgenic mice harboring temperature-sensitive simian virus 40 large T-antigen gene. Exp Cell Res. 1993 Dec;209(2):382–387. doi: 10.1006/excr.1993.1324. [DOI] [PubMed] [Google Scholar]
- Tabuchi Y., Sugiyama N., Horiuchi T., Furuhama K., Furusawa M. Biological characterization of gastric surface mucous cell line GSM06 from transgenic mice harboring temperature-sensitive simian virus 40 large T-antigen gene. Digestion. 1996;57(2):141–148. doi: 10.1159/000201328. [DOI] [PubMed] [Google Scholar]
- Takahashi M., Ota S., Shimada T., Hamada E., Kawabe T., Okudaira T., Matsumura M., Kaneko N., Terano A., Nakamura T. Hepatocyte growth factor is the most potent endogenous stimulant of rabbit gastric epithelial cell proliferation and migration in primary culture. J Clin Invest. 1995 May;95(5):1994–2003. doi: 10.1172/JCI117884. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takahashi S., Nakagawa T., Banno T., Watanabe T., Murakami K., Nakayama K. Localization of furin to the trans-Golgi network and recycling from the cell surface involves Ser and Tyr residues within the cytoplasmic domain. J Biol Chem. 1995 Nov 24;270(47):28397–28401. doi: 10.1074/jbc.270.47.28397. [DOI] [PubMed] [Google Scholar]
- Terano A., Ivey K. J., Stachura J., Sekhon S., Hosojima H., McKenzie W. N., Jr, Krause W. J., Wyche J. H. Cell culture of rat gastric fundic mucosa. Gastroenterology. 1982 Dec;83(6):1280–1291. [PubMed] [Google Scholar]
- Thomas D. M., Nasim M. M., Gullick W. J., Alison M. R. Immunoreactivity of transforming growth factor alpha in the normal adult gastrointestinal tract. Gut. 1992 May;33(5):628–631. doi: 10.1136/gut.33.5.628. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsuda T., Yoshida K., Tsujino T., Nakayama H., Kajiyama G., Tahara E. Coexpression of platelet-derived growth factor (PDGF) A-chain and PDGF receptor genes in human gastric carcinomas. Jpn J Cancer Res. 1989 Sep;80(9):813–817. doi: 10.1111/j.1349-7006.1989.tb01719.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waga S., Stillman B. Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro. Nature. 1994 May 19;369(6477):207–212. doi: 10.1038/369207a0. [DOI] [PubMed] [Google Scholar]
- Wijsman J. H., Van Dierendonck J. H., Keijzer R., van de Velde C. J., Cornelisse C. J. Immunoreactivity of proliferating cell nuclear antigen compared with bromodeoxyuridine incorporation in normal and neoplastic rat tissue. J Pathol. 1992 Sep;168(1):75–83. doi: 10.1002/path.1711680113. [DOI] [PubMed] [Google Scholar]
- van der Krol A. R., Mol J. N., Stuitje A. R. Modulation of eukaryotic gene expression by complementary RNA or DNA sequences. Biotechniques. 1988 Nov-Dec;6(10):958–976. [PubMed] [Google Scholar]