Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1985 Sep 1;101(3):1071–1077. doi: 10.1083/jcb.101.3.1071

Isolation of an adhesion-mediating protein from chick neural retina adherons

PMCID: PMC2113697  PMID: 2993313

Abstract

Adherons are high molecular weight glycoprotein complexes which are released into the growth medium of cultured cells. They mediate the adhesive interactions of many cell types, including those of embryonic chick neural retina. The cell surface receptor for chick neural retina adherons has been purified, and shown to be a heparan sulfate proteoglycan (Schubert, D., and M. LaCorbiere, 1985, J. Cell Biol., 100:56-63). This paper describes the isolation and characterization of a protein in neural retina adherons which interacts specifically with the cell surface receptor. The 20,000-mol-wt protein, called retinal purpurin (RP), stimulates neural retina cell-substratum adhesion and prolongs the survival of neural retina cells in culture. The RP protein interacts with heparin and heparan sulfate, but not with other glycosaminoglycans. Monovalent antibodies against RP inhibit RP-cell adhesion as well as adheron-cell interactions. The RP protein is found in neural retina, but not in other tissues such as brain and muscle. These data suggest that RP plays a role in both the survival and adhesive interactions of neural retina cells.

Full Text

The Full Text of this article is available as a PDF (789.9 KB).

Selected References

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

  1. Adler R., Lindsey J. D., Elsner C. L. Expression of cone-like properties by chick embryo neural retina cells in glial-free monolayer cultures. J Cell Biol. 1984 Sep;99(3):1173–1178. doi: 10.1083/jcb.99.3.1173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anderson C. W., Baum P. R., Gesteland R. F. Processing of adenovirus 2-induced proteins. J Virol. 1973 Aug;12(2):241–252. doi: 10.1128/jvi.12.2.241-252.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barbin G., Manthorpe M., Varon S. Purification of the chick eye ciliary neuronotrophic factor. J Neurochem. 1984 Nov;43(5):1468–1478. doi: 10.1111/j.1471-4159.1984.tb05410.x. [DOI] [PubMed] [Google Scholar]
  4. Brockes J. P., Lemke G. E., Balzer D. R., Jr Purification and preliminary characterization of a glial growth factor from the bovine pituitary. J Biol Chem. 1980 Sep 25;255(18):8374–8377. [PubMed] [Google Scholar]
  5. Böhlen P., Baird A., Esch F., Ling N., Gospodarowicz D. Isolation and partial molecular characterization of pituitary fibroblast growth factor. Proc Natl Acad Sci U S A. 1984 Sep;81(17):5364–5368. doi: 10.1073/pnas.81.17.5364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Carney D. H., Cunningham D. D. Initiation of check cell division by trypsin action at the cell surface. Nature. 1977 Aug 18;268(5621):602–606. doi: 10.1038/268602a0. [DOI] [PubMed] [Google Scholar]
  7. Cole G. J., Glaser L. Cell-substratum adhesion in embryonic chick central nervous system is mediated by a 170,000-mol-wt neural-specific polypeptide. J Cell Biol. 1984 Nov;99(5):1605–1612. doi: 10.1083/jcb.99.5.1605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cole G. J., Glaser L. Identification of novel neural- and neural retina-specific antigens with a monoclonal antibody. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2260–2264. doi: 10.1073/pnas.81.7.2260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cole G. J., Glaser L. Inhibition of embryonic neural retina cell-substratum adhesion with a monoclonal antibody. J Biol Chem. 1984 Apr 10;259(7):4031–4034. [PubMed] [Google Scholar]
  10. Cole G. J., Schubert D., Glaser L. Cell-substratum adhesion in chick neural retina depends upon protein-heparan sulfate interactions. J Cell Biol. 1985 Apr;100(4):1192–1199. doi: 10.1083/jcb.100.4.1192. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Conn G., Hatcher V. B. The isolation and purification of two anionic endothelial cell growth factors from human brain. Biochem Biophys Res Commun. 1984 Oct 15;124(1):262–268. doi: 10.1016/0006-291x(84)90946-x. [DOI] [PubMed] [Google Scholar]
  12. D'Amore P. A., Klagsbrun M. Endothelial cell mitogens derived from retina and hypothalamus: biochemical and biological similarities. J Cell Biol. 1984 Oct;99(4 Pt 1):1545–1549. doi: 10.1083/jcb.99.4.1545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Edgar D., Timpl R., Thoenen H. The heparin-binding domain of laminin is responsible for its effects on neurite outgrowth and neuronal survival. EMBO J. 1984 Jul;3(7):1463–1468. doi: 10.1002/j.1460-2075.1984.tb01997.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Farmbrough D. M., Fujimura F., Bonner J. Quantitative distribution of histone components in the pea plant. Biochemistry. 1968 Feb;7(2):575–585. doi: 10.1021/bi00842a010. [DOI] [PubMed] [Google Scholar]
  15. Folkman J., Moscona A. Role of cell shape in growth control. Nature. 1978 Jun 1;273(5661):345–349. doi: 10.1038/273345a0. [DOI] [PubMed] [Google Scholar]
  16. Gordon J. R., Bernfield M. R. The basal lamina of the postnatal mammary epithelium contains glycosaminoglycans in a precise ultrastructural organization. Dev Biol. 1980 Jan;74(1):118–135. doi: 10.1016/0012-1606(80)90056-1. [DOI] [PubMed] [Google Scholar]
  17. Grunwald G. B., Pratt R. S., Lilien J. Enzymic dissection of embryonic cell adhesive mechanisms. III. Immunological identification of a component of the calcium-dependent adhesive system of embryonic chick neural retina cells. J Cell Sci. 1982 Jun;55:69–83. doi: 10.1242/jcs.55.1.69. [DOI] [PubMed] [Google Scholar]
  18. Hausman R. E., Moscona A. A. Isolation of retina-specific cell-aggregating factor from membranes of embryonic neural retina tissue. Proc Natl Acad Sci U S A. 1976 Oct;73(10):3594–3598. doi: 10.1073/pnas.73.10.3594. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. MacCallum D. K., Lillie J. H., Scaletta L. J., Occhino J. C., Frederick W. G., Ledbetter S. R. Bovine corneal endothelium in vitro. Elaboration and organization and of a basement membrane. Exp Cell Res. 1982 May;139(1):1–13. doi: 10.1016/0014-4827(82)90313-5. [DOI] [PubMed] [Google Scholar]
  20. Maciag T., Mehlman T., Friesel R., Schreiber A. B. Heparin binds endothelial cell growth factor, the principal endothelial cell mitogen in bovine brain. Science. 1984 Aug 31;225(4665):932–935. doi: 10.1126/science.6382607. [DOI] [PubMed] [Google Scholar]
  21. Marchase R. B., Harges P., Jakoi E. R. Ligatin from embryonic chick neural retina inhibits retinal cell adhesion. Dev Biol. 1981 Aug;86(1):250–255. doi: 10.1016/0012-1606(81)90337-7. [DOI] [PubMed] [Google Scholar]
  22. Merrell R., Gottlieb D. I., Glaser L. Embryonal cell surface recognition. Extraction of an active plasma membrane component. J Biol Chem. 1975 Jul 25;250(14):5655–5659. [PubMed] [Google Scholar]
  23. Nishi R., Berg D. K. Two components from eye tissue that differentially stimulate the growth and development of ciliary ganglion neurons in cell culture. J Neurosci. 1981 May;1(5):505–513. doi: 10.1523/JNEUROSCI.01-05-00505.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Otsuka H., Moskowitz M. Difference in transport of leucine in attached and suspended 3T3 cells. J Cell Physiol. 1975 Jun;85(3):665–673. doi: 10.1002/jcp.1040850319. [DOI] [PubMed] [Google Scholar]
  25. Schubert D., LaCorbiere M. Isolation of a cell-surface receptor for chick neural retina adherons. J Cell Biol. 1985 Jan;100(1):56–63. doi: 10.1083/jcb.100.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schubert D., LaCorbiere M., Klier F. G., Birdwell C. A role for adherons in neural retina cell adhesion. J Cell Biol. 1983 Apr;96(4):990–998. doi: 10.1083/jcb.96.4.990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Schubert D., LaCorbiere M., Klier F. G., Birdwell C. The structure and function of myoblast adherons. Cold Spring Harb Symp Quant Biol. 1983;48(Pt 2):539–549. doi: 10.1101/sqb.1983.048.01.058. [DOI] [PubMed] [Google Scholar]
  28. Schubert D., LaCorbiere M. Properties of extracellular adhesion-mediating particles in myoblast clone and its adhesion-deficient variant. J Cell Biol. 1982 Jul;94(1):108–114. doi: 10.1083/jcb.94.1.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Thiery J. P., Brackenbury R., Rutishauser U., Edelman G. M. Adhesion among neural cells of the chick embryo. II. Purification and characterization of a cell adhesion molecule from neural retina. J Biol Chem. 1977 Oct 10;252(19):6841–6845. [PubMed] [Google Scholar]
  30. Wray W., Boulikas T., Wray V. P., Hancock R. Silver staining of proteins in polyacrylamide gels. Anal Biochem. 1981 Nov 15;118(1):197–203. doi: 10.1016/0003-2697(81)90179-2. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES