Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1976 Sep;73(9):3224–3228. doi: 10.1073/pnas.73.9.3224

Differences among sulfated proteoglycans synthesized in nonchondrogenic cells, presumptive chondroblasts, and chondroblasts.

M Okayama, M Pacifici, H Holtzer
PMCID: PMC430985  PMID: 135259

Abstract

The sulfated proteoglycans synthesized by definitive chondroblasts in cultured 10-day chick vertebral or epiphyseal cartilages were characterized by their sedimentation profile in a sucrose gradient and their susceptibility to chondroitinase ABC (EC 4.2.2.4; chondroitin ABC lyase). These sulfated proteoglycans were indistinguishable from those synthesized by definitive chondroblasts that emerge from older cultures of somites plus notochord or in older cultures of limb buds. The sulfated proteoglycans of these definitive chondroblasts are readily distinguished from those synthesized by their mother cells, the presumptive chondroblasts, or those synthesized by dedifferentiated or bromodeoxyuridine-suppressed chondroblasts. However, the sulfated proteoglycans synthesized by presumptive chondroblasts or by dedifferentiated or bromodeoxyuridine-suppressed chondroblasts cannot be dintinguished by these techniques from those synthesized by (i) blastodisc cells, (ii) fibroblasts, (iii) spinal cord cells, or (iv) skeletal, cardiac, or smooth muscle cells. Addition of glycosaminoglycans or collagen to the medium did not induce somite or limb presumptive chondroblasts to synthesize the chondroblast-unique sulfated proteoglycans. Cells moving from the presumptive chondroblast compartment into the chondroblast compartment acquire not only the option to initiate the synthesis of chondroblast-unique collagen chains, but also the capacity to synthesize chondroblast-unique sulfated proteoglycans.

Full text

PDF
3224

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abbott J., Holtzer H. The loss of phenotypic traits by differentiated cells, V. The effect of 5-bromodeoxyuridine on cloned chondrocytes. Proc Natl Acad Sci U S A. 1968 Apr;59(4):1144–1151. doi: 10.1073/pnas.59.4.1144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abbott J., Mayne R., Holtzer H. Inhibition of cartilage development in organ cultures of chick somites by the thymidine analog, 5-bromo-2'-deoxyuridine. Dev Biol. 1972 Jun;28(2):430–442. doi: 10.1016/0012-1606(72)90024-3. [DOI] [PubMed] [Google Scholar]
  3. Caplan A. I., Rosenberg M. J. Interrelationship between poly (ADP-Rib) synthesis, intracellular NAD levels, and muscle or cartilage differentiation from mesodermal cells of embryonic chick limb. Proc Natl Acad Sci U S A. 1975 May;72(5):1852–1857. doi: 10.1073/pnas.72.5.1852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chacko S., Abbott J., Holtzer S., Holtzer H. The loss of phenotypic traits by differentiated cells. VI. Behavior of the progeny of a single chondrocyte. J Exp Med. 1969 Aug 1;130(2):417–442. doi: 10.1084/jem.130.2.417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chi J. C., Fellini S. A., Holtzer H. Differences among myosins synthesized in non-myogenic cells, presumptive myoblasts, and myoblasts. Proc Natl Acad Sci U S A. 1975 Dec;72(12):4999–5003. doi: 10.1073/pnas.72.12.4999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dienstman S. R., Biehl J., Holtzer S., Holtzer H. Myogenic and chondrogenic lineages in developing limb buds grown in vitro. Dev Biol. 1974 Jul;39(1):83–95. doi: 10.1016/s0012-1606(74)80010-2. [DOI] [PubMed] [Google Scholar]
  7. Ellison M. L., Lash J. W. Environmental enhancement of in vitro chondrogenesis. Dev Biol. 1971 Nov;26(3):486–496. doi: 10.1016/0012-1606(71)90078-9. [DOI] [PubMed] [Google Scholar]
  8. Elzinga M., Maron B. J., Adelstein R. S. Human heart and platelet actins are products of different genes. Science. 1976 Jan 9;191(4222):94–95. doi: 10.1126/science.1246600. [DOI] [PubMed] [Google Scholar]
  9. Fellini S. A., Holtzer H. The localization of skeletal light meromyosin in cells of myogenic cultures. Differentiation. 1976 Aug 3;6(2):71–74. doi: 10.1111/j.1432-0436.1976.tb01471.x. [DOI] [PubMed] [Google Scholar]
  10. Goetinck P. F., Pennypacker J. P., Royal P. D. Proteochondroitin sulfate synthesis and chondrogenic expression. Exp Cell Res. 1974 Aug;87(2):241–248. doi: 10.1016/0014-4827(74)90476-5. [DOI] [PubMed] [Google Scholar]
  11. Gordon J. S., Lash J. W. In vitro chondrogenesis and cell viability. Dev Biol. 1974 Jan;36(1):88–104. doi: 10.1016/0012-1606(74)90193-6. [DOI] [PubMed] [Google Scholar]
  12. Groudine M., Holtzer H., Scherrer K., Therwath A. Lineage-dependent transcription of globin genes. Cell. 1974 Nov;3(3):243–247. doi: 10.1016/0092-8674(74)90138-x. [DOI] [PubMed] [Google Scholar]
  13. HOLTZER H. CONTROL OF CHONDROGENESIS IN THE EMBRYO. Biophys J. 1964 Jan;4:SUPPL239–SUPPL255. doi: 10.1016/s0006-3495(64)86941-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hascall V. C., Sajdera S. W. Physical properties and polydispersity of proteoglycan from bovine nasal cartilage. J Biol Chem. 1970 Oct 10;245(19):4920–4930. [PubMed] [Google Scholar]
  15. Holtzer H., Rubinstein N., Fellini S., Yeoh G., Chi J., Birnbaum J., Okayama M. Lineages, quantal cell cycles, and the generation of cell diversity. Q Rev Biophys. 1975 Nov;8(4):523–557. doi: 10.1017/s0033583500001980. [DOI] [PubMed] [Google Scholar]
  16. Keiser H., Shulman H. J., Sandson J. I. Immunochemistry of cartilage proteoglycan. Immunodiffusion and gel-electrophoretic studies. Biochem J. 1972 Jan;126(1):163–169. doi: 10.1042/bj1260163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kimata K., Okayama M., Ooira A., Suzuki S. Heterogeneity of proteochondroitin sulfates produced by chondrocytes at different stages of cytodifferentiation. J Biol Chem. 1974 Mar 10;249(5):1646–1653. [PubMed] [Google Scholar]
  18. Kosher R. A., Lash J. W., Minor R. R. Environmental enhancement of in vitro chondrogenesis. IV. Stimulation of somite chondrogenesis by exogenous chondromucoprotein. Dev Biol. 1973 Dec;35(2):210–220. doi: 10.1016/0012-1606(73)90018-3. [DOI] [PubMed] [Google Scholar]
  19. LASH J. W., HOMMES F. A., ZILLIKEN F. Induction of cell differentiation. I. The in vitro induction of vertebral cartilage with a low-molecular-weight tissue component. Biochim Biophys Acta. 1962 Jan 29;56:313–319. doi: 10.1016/0006-3002(62)90568-1. [DOI] [PubMed] [Google Scholar]
  20. Linsenmayer T. F., Toole B. P., Trelstad R. L. Temporal and spatial transitions in collagen types during embryonic chick limb development. Dev Biol. 1973 Dec;35(2):232–239. doi: 10.1016/0012-1606(73)90020-1. [DOI] [PubMed] [Google Scholar]
  21. Mayne R., Vail M. S., Miller E. J. Analysis of changes in collagen biosynthesis that occur when chick chondrocytes are grown in 5-bromo-2'-deoxyuridine. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4511–4515. doi: 10.1073/pnas.72.11.4511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Medoff J., Zwilling E. Appearance of myosin in the chick limb bud. Dev Biol. 1972 May;28(1):138–141. doi: 10.1016/0012-1606(72)90132-7. [DOI] [PubMed] [Google Scholar]
  23. Miller E. J. Structural studies on cartilage collagen employing limited cleavage and solubilization with pepsin. Biochemistry. 1972 Dec 19;11(26):4903–4909. doi: 10.1021/bi00776a005. [DOI] [PubMed] [Google Scholar]
  24. Rubinstein N., Chi J., Holtzer H. Coordinated synthesis and degradation of actin and myosin in a variety of myogenic and non-myogenic cells. Exp Cell Res. 1976 Feb;97(2):387–393. doi: 10.1016/0014-4827(76)90630-3. [DOI] [PubMed] [Google Scholar]
  25. 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]
  26. Sajdera S. W., Hascall V. C. Proteinpolysaccharide complex from bovine nasal cartilage. A comparison of low and high shear extraction procedures. J Biol Chem. 1969 Jan 10;244(1):77–87. [PubMed] [Google Scholar]
  27. Searls R. L., Janners M. Y. The stabilization of cartilage properties in the cartilage-forming mesenchyme of the embryonic chick limb. J Exp Zool. 1969 Mar;170(3):365–375. doi: 10.1002/jez.1401700313. [DOI] [PubMed] [Google Scholar]
  28. von der Mark H., von der Mark K., Gay S. Study of differential collagen synthesis during development of the chick embryo by immunofluorescence. I. Preparation of collagen type I and type II specific antibodies and their application to early stages of the chick embryo. Dev Biol. 1976 Feb;48(2):237–249. doi: 10.1016/0012-1606(76)90088-9. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES