Abstract
Glia-promoting factors (GPFs) are brain peptides which stimulate growth of specific macroglial populations in vitro. To identify the cellular sources of GPFs, we examined enriched brain cell cultures and cell lines derived from the nervous system for the production of growth factors. Ameboid microglia secreted astroglia-stimulating peptides, while growing neurons were the best source of the oligodendroglia- stimulating factors. These secretion products co-purified by gel filtration, anion exchange chromatography, and reverse-phase high performance liquid chromatography with GPFs isolated from goldfish and rat brain. Our findings suggest that glial growth in the central nervous system is regulated in part by a signaled release of peptides from specific secretory cells.
Full Text
The Full Text of this article is available as a PDF (775.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bottenstein J. E., Sato G. H. Growth of a rat neuroblastoma cell line in serum-free supplemented medium. Proc Natl Acad Sci U S A. 1979 Jan;76(1):514–517. doi: 10.1073/pnas.76.1.514. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Böhlen P., Stein S., Dairman W., Udenfriend S. Fluorometric assay of proteins in the nanogram range. Arch Biochem Biophys. 1973 Mar;155(1):213–220. doi: 10.1016/s0003-9861(73)80023-2. [DOI] [PubMed] [Google Scholar]
- Giulian D., Allen R. L., Baker T. J., Tomozawa Y. Brain peptides and glial growth. I. Glia-promoting factors as regulators of gliogenesis in the developing and injured central nervous system. J Cell Biol. 1986 Mar;102(3):803–811. doi: 10.1083/jcb.102.3.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giulian D. Isolation of ganglion cells from the retina. Brain Res. 1980 May 5;189(1):135–155. doi: 10.1016/0006-8993(80)90013-x. [DOI] [PubMed] [Google Scholar]
- Giulian D., Iwanij V., Stuckenbrok H. The response of optic tract glia during regeneration of the goldfish visual system. I. Biosynthetic activity within different glial populations after transection of retinal ganglion cell axons. Brain Res. 1985 Jul 22;339(1):87–96. doi: 10.1016/0006-8993(85)90624-9. [DOI] [PubMed] [Google Scholar]
- Giulian D., Iwanij V. The response of optic tract glia during regeneration of the goldfish visual system. II. Tectal factors stimulate optic tract glia. Brain Res. 1985 Jul 22;339(1):97–104. doi: 10.1016/0006-8993(85)90625-0. [DOI] [PubMed] [Google Scholar]
- Giulian D., Lachman L. B. Interleukin-1 stimulation of astroglial proliferation after brain injury. Science. 1985 Apr 26;228(4698):497–499. doi: 10.1126/science.3872478. [DOI] [PubMed] [Google Scholar]
- Giulian D. Peptides from the regenerating central nervous system of goldfish stimulate glia. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3567–3571. doi: 10.1073/pnas.81.11.3567. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Giulian D., Tomozawa Y., Hindman H., Allen R. L. Peptides from regenerating central nervous system promote specific populations of macroglia. Proc Natl Acad Sci U S A. 1985 Jun;82(12):4287–4290. doi: 10.1073/pnas.82.12.4287. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Illert M., Fritz N., Aschoff A., Holländer H. Fluorescent compounds as retrograde tracers compared with horseradish peroxidase (HRP). II. A parametric study in the peripheral motor system of the cat. J Neurosci Methods. 1982 Sep;6(3):199–218. doi: 10.1016/0165-0270(82)90084-x. [DOI] [PubMed] [Google Scholar]
- Lemke G. E., Brockes J. P. Identification and purification of glial growth factor. J Neurosci. 1984 Jan;4(1):75–83. doi: 10.1523/JNEUROSCI.04-01-00075.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lemmon S. K., Riley M. C., Thomas K. A., Hoover G. A., Maciag T., Bradshaw R. A. Bovine fibroblast growth factor: comparison of brain and pituitary preparations. J Cell Biol. 1982 Oct;95(1):162–169. doi: 10.1083/jcb.95.1.162. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leutz A., Schachner M. Epidermal growth factor stimulates DNA-synthesis of astrocytes in primary cerebellar cultures. Cell Tissue Res. 1981;220(2):393–404. doi: 10.1007/BF00210517. [DOI] [PubMed] [Google Scholar]
- Lim R. Glia maturation factor. Curr Top Dev Biol. 1980;16:305–322. [PubMed] [Google Scholar]
- McCarthy K. D., de Vellis J. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue. J Cell Biol. 1980 Jun;85(3):890–902. doi: 10.1083/jcb.85.3.890. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pitas R. E., Innerarity T. L., Weinstein J. N., Mahley R. W. Acetoacetylated lipoproteins used to distinguish fibroblasts from macrophages in vitro by fluorescence microscopy. Arteriosclerosis. 1981 May-Jun;1(3):177–185. doi: 10.1161/01.atv.1.3.177. [DOI] [PubMed] [Google Scholar]
- Schubert D., Heinemann S., Carlisle W., Tarikas H., Kimes B., Patrick J., Steinbach J. H., Culp W., Brandt B. L. Clonal cell lines from the rat central nervous system. Nature. 1974 May 17;249(454):224–227. doi: 10.1038/249224a0. [DOI] [PubMed] [Google Scholar]
- Thiele D. L., Kurosaka M., Lipsky P. E. Phenotype of the accessory cell necessary for mitogen-stimulated T and B cell responses in human peripheral blood: delineation by its sensitivity to the lysosomotropic agent, L-leucine methyl ester. J Immunol. 1983 Nov;131(5):2282–2290. [PubMed] [Google Scholar]
