Abstract
Mouse 3T3 cells and their Simian Virus 40-transformed derivatives (3T3SV) were used to assess the relationship of transfromation, cell density, and growth control to the cellular distribution of newly synthesized glycosaminoglycan (GAG). Glucosamine- and galactosamine- containing GAG were labeled equivalently by [3H=A1-glucose regardless of culture type, allowing incorporation into the various GAG to be compared under all conditions studied. Three components of each culture type were examined: the cells, which contain the bulk of newly synthesized GAG and are enriched in chondroitin sulfate and heparan sulfate; cell surface materials released by trypsin, which contain predominantly hyaluronic acid; and the media , which contain predominantly hyaluronic acid and undersulfated chondroitin sulfate. Increased cell density and viral transformation reduce incorporation into GAG relative to the incorporation into other polysaccharides. Transformation, however, does not substantially alter the type or distribution of newly synthesized GAG; the relative amounts and cellular distributions were very similar in 3T3 and 3T3SV cultures growing at similar rates at low densities. On the other hand, increased cell density as well as density-dependent growth inhibition modified the type and distribution of newly synthesized GAG. At high cell densities both cell types showed reduced incorporation into hyaluronate and an increase in cellular GAG due to enhanced labeling of chondroitin sulfate and heparan sulfate. These changes were more marked in confluent 3T3 cultures which also differed in showing substantially more GAG label in the medium and in chondroitin-6-sulfate and heparan sulfate at the cell surface. Since cell density and possibly density- dependent inhibition of growth but not viral transformation are major factors controlling the cellular distribution and type of newly synthesized GAG, differences due to GAG's in the culture behavior of normal and transformed cells may occur only at high cell density. The density-induced GAG alterations most likely involved are increased condroitin-6-sulfate and heparan sulfate and decreased hyaluronic acid at the cell surface.
Full Text
The Full Text of this article is available as a PDF (1.6 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bose S. K., Zlotnick B. J. Growth-and density-dependent inhibition of deoxyglucose transport in Balb 3T3 cells and its absence in cells transformed by murine sarcoma virus. Proc Natl Acad Sci U S A. 1973 Aug;70(8):2374–2378. doi: 10.1073/pnas.70.8.2374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buck C. A., Glick M. C., Warren L. Effect of growth on the glycoproteins from the surface of control and Rous sarcoma virus transformed hamster cells. Biochemistry. 1971 May 25;10(11):2176–2180. doi: 10.1021/bi00787a034. [DOI] [PubMed] [Google Scholar]
- Culp L. A., Black P. H. Contact-inhibited revertant cell lines isolated from simian virus 40-transformed cells. 3. Concanavalin A-selected revertant cells. J Virol. 1972 Apr;9(4):611–620. doi: 10.1128/jvi.9.4.611-620.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Culp L. A. Substrate-attached glycoproteins mediating adhesion of normal and virus-transformed mouse fibroblasts. J Cell Biol. 1974 Oct;63(1):71–83. doi: 10.1083/jcb.63.1.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dulbecco R. Topoinhibition and serum requirement of transformed and untransformed cells. Nature. 1970 Aug 22;227(5260):802–806. doi: 10.1038/227802a0. [DOI] [PubMed] [Google Scholar]
- Gail M. H., Boone C. W. Cell-substrate adhesivity. A determinant of cell motility. Exp Cell Res. 1972 Jan;70(1):33–40. doi: 10.1016/0014-4827(72)90178-4. [DOI] [PubMed] [Google Scholar]
- Gail M. H., Boone C. W. Density inhibition of motility in 3T3 fibroblasts and their SV40 transformants. Exp Cell Res. 1971 Jan;64(1):156–162. doi: 10.1016/0014-4827(71)90206-0. [DOI] [PubMed] [Google Scholar]
- Goggins J. F., Johnson G. S., Pastan I. The effect of dibutyryl cyclic adenosine monophosphate on synthesis of sulfated acid mucopolysaccharides by transformed fibroblasts. J Biol Chem. 1972 Sep 25;247(18):5759–5764. [PubMed] [Google Scholar]
- Goto M., Kataoka Y., Kimura T., Goto K., Sato H. Decrease of saturation density of cells of hamster cell lines after treatment with dextran sulfate. Exp Cell Res. 1973 Dec;82(2):367–374. doi: 10.1016/0014-4827(73)90354-6. [DOI] [PubMed] [Google Scholar]
- Guss J. M., Hukins D. W., Smith P. J., Winter W. T., Arnott S. Hyaluronic acid: molecular conformations and interactions in two sodium salts. J Mol Biol. 1975 Jul 5;95(3):359–384. doi: 10.1016/0022-2836(75)90196-5. [DOI] [PubMed] [Google Scholar]
- Hamerman D., Todaro G. J., Green H. The production of hyaluronate by spontaneously established cell lines and viral transformed lines of fibroblastic origin. Biochim Biophys Acta. 1965 Nov 1;101(3):343–351. doi: 10.1016/0926-6534(65)90013-8. [DOI] [PubMed] [Google Scholar]
- Hök M., Lindahl U., Bäckström G., Malmström A., Fransson L. Biosynthesis of heparin. 3. Formation of iduronic acid residues. J Biol Chem. 1974 Jun 25;249(12):3908–3915. [PubMed] [Google Scholar]
- Isselbacher K. J. Increased uptake of amino acids and 2-deoxy-D-glucose by virus-transformed cells in culture. Proc Natl Acad Sci U S A. 1972 Mar;69(3):585–589. doi: 10.1073/pnas.69.3.585. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson G. S., Pastan I. Role of 3',5'-adenosine monophosphate in regulation of morphology and growth of transformed and normal fibroblasts. J Natl Cancer Inst. 1972 May;48(5):1377–1387. [PubMed] [Google Scholar]
- Kosher R. A., Searls R. L. Sulfated mucopolysaccharide synthesis during the development of Rana pipiens. Dev Biol. 1973 May;32(1):50–68. doi: 10.1016/0012-1606(73)90219-4. [DOI] [PubMed] [Google Scholar]
- Kraemer P. M., Smith D. A. High molecular-weight heparan sulfate from the cell surface. Biochem Biophys Res Commun. 1974 Jan 23;56(2):423–430. doi: 10.1016/0006-291x(74)90859-6. [DOI] [PubMed] [Google Scholar]
- Kraemer P. M., Tobey R. A. Cell-cycle dependent desquamation of heparan sulfate from the cell surface. J Cell Biol. 1972 Dec;55(3):713–717. doi: 10.1083/jcb.55.3.713. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LINKER A., HOFFMAN P., MEYER K., SAMPSON P., KORN E. D. The formation of unsaturated disacharides from mucopoly-saccharides and their cleavage to alpha-keto acid by bacterial enzymes. J Biol Chem. 1960 Nov;235:3061–3065. [PubMed] [Google Scholar]
- Martinez-Palomo A., Braislovsky C., Bernhard W. Ultrastructural modifications of the cell surface and intercellular contacts of some transformed cell strains. Cancer Res. 1969 Apr;29(4):925–937. [PubMed] [Google Scholar]
- Meezan E., Wu H. C., Black P. H., Robbins P. W. Comparative studies on the carbohydrate-containing membrane components of normal and virus-transformed mouse fibroblasts. II. Separation of glycoproteins and glycopeptides by sephadex chromatography. Biochemistry. 1969 Jun;8(6):2518–2524. doi: 10.1021/bi00834a039. [DOI] [PubMed] [Google Scholar]
- Meier S., Hay E. D. Stimulation of extracellular matrix synthesis in the developing cornea by glycosaminoglycans. Proc Natl Acad Sci U S A. 1974 Jun;71(6):2310–2313. doi: 10.1073/pnas.71.6.2310. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Noonan K. D., Burger M. M. Binding of ( 3 H)concanavalin A to normal and transformed cells. J Biol Chem. 1973 Jun 25;248(12):4286–4292. [PubMed] [Google Scholar]
- OYAMA V. I., EAGLE H. Measurement of cell growth in tissue culture with a phenol reagent (folin-ciocalteau). Proc Soc Exp Biol Med. 1956 Feb;91(2):305–307. doi: 10.3181/00379727-91-22245. [DOI] [PubMed] [Google Scholar]
- Pessac B., Defendi V. Cell aggregation: role of acid mucopolysaccharides. Science. 1972 Feb 25;175(4024):898–900. doi: 10.1126/science.175.4024.898. [DOI] [PubMed] [Google Scholar]
- Roblin R., Albert S. O., Gelb N. A., Black P. H. Cell surface changes correlated with density-dependent growth inhibition. Glycosaminoglycan metabolism in 3T3, SV3T3, and con A selected revertant cells. Biochemistry. 1975 Jan 28;14(2):347–357. doi: 10.1021/bi00673a022. [DOI] [PubMed] [Google Scholar]
- STROMINGER J. L. Uridine and guanosine nucleotides of hen oviduct. J Biol Chem. 1962 May;237:1388–1392. [PubMed] [Google Scholar]
- Saito H., Uzman B. G. Production and secretion of chondroitin sulfates and dermatan sulfate by established mammalian cell lines. Biochem Biophys Res Commun. 1971 May 21;43(4):723–728. doi: 10.1016/0006-291x(71)90675-9. [DOI] [PubMed] [Google Scholar]
- Saito H., Yamagata T., Suzuki S. Enzymatic methods for the determination of small quantities of isomeric chondroitin sulfates. J Biol Chem. 1968 Apr 10;243(7):1536–1542. [PubMed] [Google Scholar]
- Sakiyama H., Burge B. W. Comparative studies of the carbohydrate-containing components of 3T3 and simian virus 40 transformed 3T3 mouse fibroblasts. Biochemistry. 1972 Apr 11;11(8):1366–1377. doi: 10.1021/bi00758a007. [DOI] [PubMed] [Google Scholar]
- Satoh C., Duff R., Rapp F., Davidson E. A. Production of mucopolysaccharides by normal and transformed cells. Proc Natl Acad Sci U S A. 1973 Jan;70(1):54–56. doi: 10.1073/pnas.70.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schultz A. R., Culp L. A. Contact-inhibited revertant cell lines isolated from SV40-transformed cells. V. Contact inhibition of sugar transport. Exp Cell Res. 1973 Sep;81(1):95–103. doi: 10.1016/0014-4827(73)90115-8. [DOI] [PubMed] [Google Scholar]
- Schönhöfer P. S., Peters H. D., Karzel K., Dinnendahl V., Westhofen P. Influence of antiphlogistic drugs on prostaglandin E1 stimulated cyclic 3',5'-AMP levels and glycosaminoglycan synthesis in fibroblast tissue cultures. Pol J Pharmacol Pharm. 1974 Jan-Apr;26(1):51–60. [PubMed] [Google Scholar]
- Shapiro S. S., Sherman M. I. Sulfated mucopolysaccharides of midgestation embryonic and extraembryonic tissues of the mouse. Arch Biochem Biophys. 1974 May;162(1):272–280. doi: 10.1016/0003-9861(74)90126-x. [DOI] [PubMed] [Google Scholar]
- Shields R., Pollock K. The adhesion of BHK and PyBHK cells to the substratum. Cell. 1974 Sep;3(1):31–38. doi: 10.1016/0092-8674(74)90034-8. [DOI] [PubMed] [Google Scholar]
- Suzuki S., Saito H., Yamagata T., Anno K., Seno N., Kawai Y., Furuhashi T. Formation of three types of disulfated disaccharides from chondroitin sulfates by chondroitinase digestion. J Biol Chem. 1968 Apr 10;243(7):1543–1550. [PubMed] [Google Scholar]
- Terry A. H., Culp L. A. Substrate-attached glycoproteins from normal and virus-transformed cells. Biochemistry. 1974 Jan 29;13(3):414–425. doi: 10.1021/bi00700a004. [DOI] [PubMed] [Google Scholar]
- Toole B. P., Trelstad R. L. Hyaluronate production and removal during corneal development in the chick. Dev Biol. 1971 Sep;26(1):28–35. doi: 10.1016/0012-1606(71)90104-7. [DOI] [PubMed] [Google Scholar]
- Yamagata T., Saito H., Habuchi O., Suzuki S. Purification and properties of bacterial chondroitinases and chondrosulfatases. J Biol Chem. 1968 Apr 10;243(7):1523–1535. [PubMed] [Google Scholar]
- Yamamoto K., Terayama H. Comparison of cell coat acid mucopolysaccharides of normal liver and various ascites hepatoma cells. Cancer Res. 1973 Oct;33(10):2257–2264. [PubMed] [Google Scholar]