Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1991 Jan 2;112(2):313–322. doi: 10.1083/jcb.112.2.313

Purification and characterization of an 82-kD membrane protein as a neurite outgrowth factor binding protein: possible involvement of NOF binding protein in axonal outgrowth in developing retina

PMCID: PMC2288814  PMID: 1988463

Abstract

Neurite outgrowth factor (NOF) is a glycoprotein isolated from an extract of gizzard that induces neurite outgrowth from cultured retinal or ciliary ganglionic (CG) neurons. We have reported that a glycoprotein of approximately 82 kD solubilized from gizzard muscles binds to NOF (ligand blotting) and inhibits the neurite promoting activity of NOF (inhibition assay). The 82-kD protein (NOF binding protein) was purified from gizzard muscle membranes as a doublet band on SDS-PAGE and a polyclonal antibody was raised against it. An NOF binding protein in developing retina exhibited the same physicochemical properties as that of the gizzard muscle. Quantitative decrease in NOF binding protein in embryonic retinas was observed after day 11 by the inhibition assay, ligand blotting, and immunoblotting, its decrease being parallel with reduction of NOF-induced neurite outgrowth of embryonic retinas. In an immunohistochemical study, the antibody stained only the optic fiber layers of the retinas of 8-d embryos, and this staining was no longer detectable in retinas of 18-d embryos. These results suggest that the 82-kD protein is a novel membrane protein that behaves as an NOF receptor and that the loss of neuritic response of the retinal neurons to NOF reflects a decrease in NOF receptor molecules.

Full Text

The Full Text of this article is available as a PDF (2.9 MB).

Selected References

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

  1. Bordier C. Phase separation of integral membrane proteins in Triton X-114 solution. J Biol Chem. 1981 Feb 25;256(4):1604–1607. [PubMed] [Google Scholar]
  2. Bozyczko D., Horwitz A. F. The participation of a putative cell surface receptor for laminin and fibronectin in peripheral neurite extension. J Neurosci. 1986 May;6(5):1241–1251. doi: 10.1523/JNEUROSCI.06-05-01241.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cohen J., Nurcombe V., Jeffrey P., Edgar D. Developmental loss of functional laminin receptors on retinal ganglion cells is regulated by their target tissue, the optic tectum. Development. 1989 Oct;107(2):381–387. doi: 10.1242/dev.107.2.381. [DOI] [PubMed] [Google Scholar]
  4. Graf J., Iwamoto Y., Sasaki M., Martin G. R., Kleinman H. K., Robey F. A., Yamada Y. Identification of an amino acid sequence in laminin mediating cell attachment, chemotaxis, and receptor binding. Cell. 1987 Mar 27;48(6):989–996. doi: 10.1016/0092-8674(87)90707-0. [DOI] [PubMed] [Google Scholar]
  5. Hayashi Y., Higashida H., Kuo C., Miki N. Antiserum against neurite outgrowth factor in chick gizzard extract and its inhibitory effect on neuritic response in cultured ciliary neurons. J Neurochem. 1984 Feb;42(2):504–512. doi: 10.1111/j.1471-4159.1984.tb02706.x. [DOI] [PubMed] [Google Scholar]
  6. Hayashi Y., Miki N. Purification and characterization of a neurite outgrowth factor from chicken gizzard smooth muscle. J Biol Chem. 1985 Nov 15;260(26):14269–14278. [PubMed] [Google Scholar]
  7. Hayashi Y., Taniura H., Miki N. Interaction of monoclonal antibodies with a neurite outgrowth factor from chicken gizzard extract. Brain Res. 1987 Sep;432(1):11–19. doi: 10.1016/0165-3806(87)90003-4. [DOI] [PubMed] [Google Scholar]
  8. Hopkins J. M., Ford-Holevinski T. S., McCoy J. P., Agranoff B. W. Laminin and optic nerve regeneration in the goldfish. J Neurosci. 1985 Nov;5(11):3030–3038. doi: 10.1523/JNEUROSCI.05-11-03030.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hunter D. D., Shah V., Merlie J. P., Sanes J. R. A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction. Nature. 1989 Mar 16;338(6212):229–234. doi: 10.1038/338229a0. [DOI] [PubMed] [Google Scholar]
  10. Kato S., Negishi K., Hayashi Y., Miki N. Enhancement of neurite outgrowth and aspartate-glutamate uptake systems in retinal explants cultured with chick gizzard extract. J Neurochem. 1983 Apr;40(4):929–938. doi: 10.1111/j.1471-4159.1983.tb08076.x. [DOI] [PubMed] [Google Scholar]
  11. Kleinman H. K., Ogle R. C., Cannon F. B., Little C. D., Sweeney T. M., Luckenbill-Edds L. Laminin receptors for neurite formation. Proc Natl Acad Sci U S A. 1988 Feb;85(4):1282–1286. doi: 10.1073/pnas.85.4.1282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  13. Letourneau P. C., Madsen A. M., Palm S. L., Furcht L. T. Immunoreactivity for laminin in the developing ventral longitudinal pathway of the brain. Dev Biol. 1988 Jan;125(1):135–144. doi: 10.1016/0012-1606(88)90066-8. [DOI] [PubMed] [Google Scholar]
  14. Liesi P. Do neurons in the vertebrate CNS migrate on laminin? EMBO J. 1985 May;4(5):1163–1170. doi: 10.1002/j.1460-2075.1985.tb03755.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Liesi P. Laminin-immunoreactive glia distinguish regenerative adult CNS systems from non-regenerative ones. EMBO J. 1985 Oct;4(10):2505–2511. doi: 10.1002/j.1460-2075.1985.tb03963.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Menko A. S., Boettiger D. Occupation of the extracellular matrix receptor, integrin, is a control point for myogenic differentiation. Cell. 1987 Oct 9;51(1):51–57. doi: 10.1016/0092-8674(87)90009-2. [DOI] [PubMed] [Google Scholar]
  17. Miki N., Hayashi Y., Higashida H. Characterization of chick gizzard extract that promotes neurite outgrowth in cultured ciliary neurons. J Neurochem. 1981 Sep;37(3):627–633. doi: 10.1111/j.1471-4159.1982.tb12533.x. [DOI] [PubMed] [Google Scholar]
  18. Ruoslahti E. Fibronectin and its receptors. Annu Rev Biochem. 1988;57:375–413. doi: 10.1146/annurev.bi.57.070188.002111. [DOI] [PubMed] [Google Scholar]
  19. Ruoslahti E., Pierschbacher M. D. Arg-Gly-Asp: a versatile cell recognition signal. Cell. 1986 Feb 28;44(4):517–518. doi: 10.1016/0092-8674(86)90259-x. [DOI] [PubMed] [Google Scholar]
  20. Taniura H., Hayashi Y., Miki N. An 82-kilodalton membrane protein that inhibits the activity of neurite outgrowth factor. J Neurochem. 1988 May;50(5):1572–1578. doi: 10.1111/j.1471-4159.1988.tb03046.x. [DOI] [PubMed] [Google Scholar]
  21. Tomaselli K. J., Reichardt L. F., Bixby J. L. Distinct molecular interactions mediate neuronal process outgrowth on non-neuronal cell surfaces and extracellular matrices. J Cell Biol. 1986 Dec;103(6 Pt 2):2659–2672. doi: 10.1083/jcb.103.6.2659. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES