Abstract
Several sugar structures have been reported to be necessary for haemopoiesis. We analysed the haematological phenotypes of transgenic mice expressing beta-1,4 N-acetylglucosaminyltransferase III (GnT-III), which forms bisecting N-acetylglucosamine on asparagine-linked oligosaccharides. In the transgenic mice, the GnT-III activity was elevated in bone marrow, spleen and peripheral blood and in isolated mononuclear cells from these tissues, whereas no activity was found in these tissues of wild-type mice. Stromal cells after long-term cultures of transgenic-derived bone marrow and spleen cells also showed elevated GnT-III activity, compared with an undetectable activity in wild-type stromal cells. As judged by HPLC analysis, lectin blotting and lectin cytotoxicity assay, bisecting GlcNAc residues were increased on both blood cells and stromal cells from bone marrow and spleen in transgenic mice. The transgenic mice displayed spleen atrophy, hypocellular bone marrow and pancytopenia. Bone marrow cells and spleen cells from transgenic mice produced fewer haemopoietic colonies. After lethal irradiation followed by bone marrow transplantation, transgenic recipient mice showed pancytopenia compared with wild-type recipient mice. Bone marrow cells from transgenic donors gave haematological reconstitution at the same level as wild-type donor cells. In addition, non-adherent cell production was decreased in long-term bone marrow cell cultures of transgenic mice. Collectively these results indicate that the stroma-supported haemopoiesis is compromised in transgenic mice expressing GnT-III, providing the first demonstration that the N-glycans have some significant roles in stroma-dependent haemopoiesis.
Full Text
The Full Text of this article is available as a PDF (622.0 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aizawa S., Tavassoli M. Kinetics of inhibition of CFU-C homing in long-term marrow culture. Exp Hematol. 1988 Mar;16(3):217–220. [PubMed] [Google Scholar]
- Aizawa S., Tavassoli M. Molecular basis of the recognition of intravenously transplanted hemopoietic cells by bone marrow. Proc Natl Acad Sci U S A. 1988 May;85(9):3180–3183. doi: 10.1073/pnas.85.9.3180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bhaumik M., Seldin M. F., Stanley P. Cloning and chromosomal mapping of the mouse Mgat3 gene encoding N-acetylglucosaminyltransferase III. Gene. 1995 Oct 27;164(2):295–300. doi: 10.1016/0378-1119(95)00260-d. [DOI] [PubMed] [Google Scholar]
- Cummings R. D., Kornfeld S. Characterization of the structural determinants required for the high affinity interaction of asparagine-linked oligosaccharides with immobilized Phaseolus vulgaris leukoagglutinating and erythroagglutinating lectins. J Biol Chem. 1982 Oct 10;257(19):11230–11234. [PubMed] [Google Scholar]
- Fujii S., Nishiura T., Nishikawa A., Miura R., Taniguchi N. Structural heterogeneity of sugar chains in immunoglobulin G. Conformation of immunoglobulin G molecule and substrate specificities of glycosyltransferases. J Biol Chem. 1990 Apr 15;265(11):6009–6018. [PubMed] [Google Scholar]
- Gallatin M., St John T. P., Siegelman M., Reichert R., Butcher E. C., Weissman I. L. Lymphocyte homing receptors. Cell. 1986 Mar 14;44(5):673–680. doi: 10.1016/0092-8674(86)90832-9. [DOI] [PubMed] [Google Scholar]
- Ioffe E., Stanley P. Mice lacking N-acetylglucosaminyltransferase I activity die at mid-gestation, revealing an essential role for complex or hybrid N-linked carbohydrates. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):728–732. doi: 10.1073/pnas.91.2.728. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kobata A., Yamashita K. Affinity chromatography of oligosaccharides on E4-phytohemagglutinin-agarose column. Methods Enzymol. 1989;179:46–54. doi: 10.1016/0076-6879(89)79112-6. [DOI] [PubMed] [Google Scholar]
- Kornfeld R., Ferris C. Interaction of immunoglobulin glycopeptides with concanavalin A. J Biol Chem. 1975 Apr 10;250(7):2614–2619. [PubMed] [Google Scholar]
- Kumar R., Yang J., Larsen R. D., Stanley P. Cloning and expression of N-acetylglucosaminyltransferase I, the medial Golgi transferase that initiates complex N-linked carbohydrate formation. Proc Natl Acad Sci U S A. 1990 Dec;87(24):9948–9952. doi: 10.1073/pnas.87.24.9948. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lasky L. A. Selectins: interpreters of cell-specific carbohydrate information during inflammation. Science. 1992 Nov 6;258(5084):964–969. doi: 10.1126/science.1439808. [DOI] [PubMed] [Google Scholar]
- Long M. W. Blood cell cytoadhesion molecules. Exp Hematol. 1992 Mar;20(3):288–301. [PubMed] [Google Scholar]
- Metzler M., Gertz A., Sarkar M., Schachter H., Schrader J. W., Marth J. D. Complex asparagine-linked oligosaccharides are required for morphogenic events during post-implantation development. EMBO J. 1994 May 1;13(9):2056–2065. doi: 10.1002/j.1460-2075.1994.tb06480.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miyoshi E., Ihara Y., Hayashi N., Fusamoto H., Kamada T., Taniguchi N. Transfection of N-acetylglucosaminyltransferase III gene suppresses expression of hepatitis B virus in a human hepatoma cell line, HB611. J Biol Chem. 1995 Nov 24;270(47):28311–28315. doi: 10.1074/jbc.270.47.28311. [DOI] [PubMed] [Google Scholar]
- Narasimhan S. Control of glycoprotein synthesis. UDP-GlcNAc:glycopeptide beta 4-N-acetylglucosaminyltransferase III, an enzyme in hen oviduct which adds GlcNAc in beta 1-4 linkage to the beta-linked mannose of the trimannosyl core of N-glycosyl oligosaccharides. J Biol Chem. 1982 Sep 10;257(17):10235–10242. [PubMed] [Google Scholar]
- Nishikawa A., Fujii S., Sugiyama T., Taniguchi N. A method for the determination of N-acetylglucosaminyltransferase III activity in rat tissues involving HPLC. Anal Biochem. 1988 May 1;170(2):349–354. doi: 10.1016/0003-2697(88)90641-0. [DOI] [PubMed] [Google Scholar]
- Nishikawa A., Ihara Y., Hatakeyama M., Kangawa K., Taniguchi N. Purification, cDNA cloning, and expression of UDP-N-acetylglucosamine: beta-D-mannoside beta-1,4N-acetylglucosaminyltransferase III from rat kidney. J Biol Chem. 1992 Sep 5;267(25):18199–18204. [PubMed] [Google Scholar]
- Okada Y., Spiro R. G. Isolation and characterization of three major glycoproteins from thyroid plasma membranes. J Biol Chem. 1980 Sep 25;255(18):8865–8872. [PubMed] [Google Scholar]
- Sarkar M., Hull E., Nishikawa Y., Simpson R. J., Moritz R. L., Dunn R., Schachter H. Molecular cloning and expression of cDNA encoding the enzyme that controls conversion of high-mannose to hybrid and complex N-glycans: UDP-N-acetylglucosamine: alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I. Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):234–238. doi: 10.1073/pnas.88.1.234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stanley P. Selection of specific wheat germ agglutinin-resistant (WgaR) phenotypes from Chinese hamster ovary cell populations containing numerous lecR genotypes. Mol Cell Biol. 1981 Aug;1(8):687–696. doi: 10.1128/mcb.1.8.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stoolman L. M., Rosen S. D. Possible role for cell-surface carbohydrate-binding molecules in lymphocyte recirculation. J Cell Biol. 1983 Mar;96(3):722–729. doi: 10.1083/jcb.96.3.722. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sullenbarger B. A., Petitt M. S., Chong P., Long M. W., Wicha M. S. Murine granulocytic cell adhesion to bone marrow hemonectin is mediated by mannose and galactose. Blood. 1995 Jul 1;86(1):135–140. [PubMed] [Google Scholar]
- Taniguchi N., Yoshimura M., Miyoshi E., Ihara Y., Nishikawa A., Fujii S. Remodeling of cell surface glycoproteins by N-acetylglucosaminyltransferase III gene transfection: modulation of metastatic potentials and down regulation of hepatitis B virus replication. Glycobiology. 1996 Oct;6(7):691–694. doi: 10.1093/glycob/6.7.691. [DOI] [PubMed] [Google Scholar]
- Tokugawa K., Oguri S., Takeuchi M. Large scale preparation of PA-oligosaccharides from glycoproteins using an improved extraction method. Glycoconj J. 1996 Feb;13(1):53–56. [PubMed] [Google Scholar]
- Yamashita K., Hitoi A., Kobata A. Structural determinants of Phaseolus vulgaris erythroagglutinating lectin for oligosaccharides. J Biol Chem. 1983 Dec 25;258(24):14753–14755. [PubMed] [Google Scholar]
- Yoshimura M., Ihara Y., Matsuzawa Y., Taniguchi N. Aberrant glycosylation of E-cadherin enhances cell-cell binding to suppress metastasis. J Biol Chem. 1996 Jun 7;271(23):13811–13815. doi: 10.1074/jbc.271.23.13811. [DOI] [PubMed] [Google Scholar]
- Yoshimura M., Ihara Y., Ohnishi A., Ijuhin N., Nishiura T., Kanakura Y., Matsuzawa Y., Taniguchi N. Bisecting N-acetylglucosamine on K562 cells suppresses natural killer cytotoxicity and promotes spleen colonization. Cancer Res. 1996 Jan 15;56(2):412–418. [PubMed] [Google Scholar]
- Yoshimura M., Nishikawa A., Ihara Y., Nishiura T., Nakao H., Kanayama Y., Matuzawa Y., Taniguchi N. High expression of UDP-N-acetylglucosamine: beta-D mannoside beta-1,4-N-acetylglucosaminyltransferase III (GnT-III) in chronic myelogenous leukemia in blast crisis. Int J Cancer. 1995 Feb 8;60(4):443–449. doi: 10.1002/ijc.2910600404. [DOI] [PubMed] [Google Scholar]
- Yoshimura M., Nishikawa A., Ihara Y., Taniguchi S., Taniguchi N. Suppression of lung metastasis of B16 mouse melanoma by N-acetylglucosaminyltransferase III gene transfection. Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8754–8758. doi: 10.1073/pnas.92.19.8754. [DOI] [PMC free article] [PubMed] [Google Scholar]