Literature DB >> 7085777

Mitogenicity of brain axolemma membranes and soluble factors for dorsal root ganglion Schwann cells.

D Cassel, P M Wood, R P Bunge, L Glaser.   

Abstract

Previous studies in this laboratory have shown that membranes derived from dorsal root ganglia (DRG) neurites are mitogenic for cultured Schwann cells derived from the same source [Salzer et al (1980): J Cell Biol 84:767-778]. Improved procedures are described for preparing Schwann cells derived from dorsal root ganglia that are highly responsive to various mitogens. Under these conditions, the cells respond not only to the neurite mitogen but also to pituitary extracts, dibutyryl cyclic AMP, and cholera toxin that have been shown previously to be good mitogens for Schwann cells derived from sciatic nerve [Raff et al (1978): Cell 15:813-822], thus reconciling discrepancies in the response of these different Schwann cell preparations to mitogens. Searching for a source of membranes more suitable for biochemical characterization of the neurite mitogen, we found that bovine brain axolemma, prepared by the method of DeVries et al [(1977):Brain Res 147:339-352] is highly mitogenic for Schwann cells. The mitotic index of Schwann cells was increased by the addition of axolemma from 0.5%-2% to 30%-50% during 24-h incubation with [3H]thymidine. Half maximal effect was obtained at about 0.4 microgram axolemma protein per microwell containing 2-4 X 10(3) cells. The axolemma mitogen appears to be an integral membrane protein that remains bound to the membrane under various ionic conditions but can be extracted in a partially active form with deoxycholate. Like the DRG neurite mitogen, the mitogenic activity of axolemma was abolished by trypsin treatment. Unlike the neurite preparation, however, the mitogenic activity of axolemma was only partially inactivated by heat treatment (60%-70% inactivation). A significant difference between the mitogenic activity of axolemma membranes and neurite membranes is the fact that axolemma membranes fail to stimulate Schwann cell proliferation in a defined, serum-free medium (N-2), whereas neurites show significant mitogenic activity in this medium. These findings indicate a possible difference between DRG neurites and brain axolemma either in the mitogen itself or surface components responsible for recognition between the membranes and the cells.

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Year:  1982        PMID: 7085777     DOI: 10.1002/jcb.1982.240180405

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  13 in total

1.  The neuronal cell-surface molecule mitogenic for Schwann cells is a heparin-binding protein.

Authors:  N Ratner; D M Hong; M A Lieberman; R P Bunge; L Glaser
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

2.  Release of autocrine growth factor by primary and immortalized Schwann cells.

Authors:  S Porter; L Glaser; R P Bunge
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

Review 3.  Multicellular spheroids. A review on cellular aggregates in cancer research.

Authors:  W Mueller-Klieser
Journal:  J Cancer Res Clin Oncol       Date:  1987       Impact factor: 4.553

4.  Insulin growth factors regulate the mitotic cycle in cultured rat sympathetic neuroblasts.

Authors:  E DiCicco-Bloom; I B Black
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

5.  Control of myogenic differentiation by fibroblast growth factor is mediated by position in the G1 phase of the cell cycle.

Authors:  B Lathrop; K Thomas; L Glaser
Journal:  J Cell Biol       Date:  1985-12       Impact factor: 10.539

6.  Platelet-derived growth factors and fibroblast growth factors are mitogens for rat Schwann cells.

Authors:  J B Davis; P Stroobant
Journal:  J Cell Biol       Date:  1990-04       Impact factor: 10.539

7.  PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division.

Authors:  N Ratner; L Glaser; R P Bunge
Journal:  J Cell Biol       Date:  1984-03       Impact factor: 10.539

8.  Selective induction of tyrosine hydroxylase by cell-cell contact in bovine adrenal chromaffin cells is mimicked by plasma membranes.

Authors:  S Saadat; H Thoenen
Journal:  J Cell Biol       Date:  1986-11       Impact factor: 10.539

9.  Spheroidal aggregate culture of rat liver cells: histotypic reorganization, biomatrix deposition, and maintenance of functional activities.

Authors:  J Landry; D Bernier; C Ouellet; R Goyette; N Marceau
Journal:  J Cell Biol       Date:  1985-09       Impact factor: 10.539

10.  A neuronal cell surface heparan sulfate proteoglycan is required for dorsal root ganglion neuron stimulation of Schwann cell proliferation.

Authors:  N Ratner; R P Bunge; L Glaser
Journal:  J Cell Biol       Date:  1985-09       Impact factor: 10.539

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