Literature DB >> 2277078

Schwann cell proliferation in vitro is under negative autocrine control.

D Muir1, S Varon, M Manthorpe.   

Abstract

In healthy adult peripheral nerve, Schwann cells are believed to be generally quiescent. Similarly, cultures of isolated rat sciatic nerve Schwann cells hardly proliferate in serum-supplemented medium. The possibility that Schwann cells negatively regulate their own proliferation was supported by the demonstration that conditioned media from Schwann cell cultures inhibited the proliferation of mitogen-stimulated test cultures. The inhibition could be complete, was dose dependent, and was exhibited when the test Schwann cells were under the influence of different types of mitogens such as cholera toxin, laminin, and living neurons. The inhibition of proliferation was completely reversible and a rapid doubling of cell number resulted when treatment with conditioned medium was withdrawn from mitogen-stimulated Schwann cells. Conditioned medium from cholera toxin-stimulated and immortalized Schwann cell cultures contained less antiproliferative activity than that found in medium from quiescent Schwann cell cultures. However, media conditioned by two actively proliferating rat Schwannoma cell lines were rich sources of antiproliferative activity for Schwann cells. Unlike the mitogen-stimulated Schwann cells, whose proliferation could be inhibited completely, the immortalized and transformed Schwann cell types were nearly unresponsive to the antiproliferative activity. The antiproliferative activity in Schwann and Schwannoma cell conditioned media was submitted to gel filtration and SDS-PAGE. The activity exists in at least two distinct forms: (a) a high molecular weight complex with an apparent molecular mass greater than 1,000 kD, and (b) a lower molecular weight form having a molecular mass of 55 kD. The active 55-kD form could be derived from the high molecular weight form by gel filtration performed under dissociating conditions. The 55-kD form was further purified to electrophoretic homogeneity. These results suggest that Schwann cells produce an autocrine factor, which we designate as a "neural antiproliferative protein," which completely inhibits the in vitro proliferation of Schwann cells but not that of immortalized Schwann cells or Schwannoma lines.

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Year:  1990        PMID: 2277078      PMCID: PMC2116433          DOI: 10.1083/jcb.111.6.2663

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  27 in total

1.  Separation of functional Schwann cells and neurons from normal peripheral nerve tissue.

Authors:  P M Wood
Journal:  Brain Res       Date:  1976-10-22       Impact factor: 3.252

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Authors:  H Towbin; T Staehelin; J Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

3.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

4.  Studies on cultured rat Schwann cells. I. Establishment of purified populations from cultures of peripheral nerve.

Authors:  J P Brockes; K L Fields; M C Raff
Journal:  Brain Res       Date:  1979-04-06       Impact factor: 3.252

5.  An enzyme-linked immunosorbent assay for bromodeoxyuridine incorporation using fixed microcultures.

Authors:  D Muir; S Varon; M Manthorpe
Journal:  Anal Biochem       Date:  1990-03       Impact factor: 3.365

6.  Purification of mouse Schwann cells using neurite-induced proliferation in serum-free monolayer culture.

Authors:  M Manthorpe; S Skaper; S Varon
Journal:  Brain Res       Date:  1980-09-08       Impact factor: 3.252

7.  Studies of Schwann cell proliferation. I. An analysis in tissue culture of proliferation during development, Wallerian degeneration, and direct injury.

Authors:  J L Salzer; R P Bunge
Journal:  J Cell Biol       Date:  1980-03       Impact factor: 10.539

8.  Growth control in cultured 3T3 fibroblasts. Assays of cell proliferation and demonstration of a growth inhibitory activity.

Authors:  P A Steck; P G Voss; J L Wang
Journal:  J Cell Biol       Date:  1979-12       Impact factor: 10.539

9.  Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.

Authors:  K D McCarthy; J de Vellis
Journal:  J Cell Biol       Date:  1980-06       Impact factor: 10.539

10.  Studies of Schwann cell proliferation. III. Evidence for the surface localization of the neurite mitogen.

Authors:  J L Salzer; R P Bunge; L Glaser
Journal:  J Cell Biol       Date:  1980-03       Impact factor: 10.539

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  6 in total

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Authors:  C Meier; E Parmantier; A Brennan; R Mirsky; K R Jessen
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

2.  Early mutation of the neu (erbB-2) gene during ethylnitrosourea-induced oncogenesis in the rat Schwann cell lineage.

Authors:  L A Ballering; J Lyons; M F Rajewsky
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-15       Impact factor: 11.205

3.  Differences in proliferation and invasion by normal, transformed and NF1 Schwann cell cultures are influenced by matrix metalloproteinase expression.

Authors:  D Muir
Journal:  Clin Exp Metastasis       Date:  1995-07       Impact factor: 5.150

4.  The effects of cAMP on differentiation of cultured Schwann cells: progression from an early phenotype (04+) to a myelin phenotype (P0+, GFAP-, N-CAM-, NGF-receptor-) depends on growth inhibition.

Authors:  L Morgan; K R Jessen; R Mirsky
Journal:  J Cell Biol       Date:  1991-02       Impact factor: 10.539

5.  Satellite cell proliferation in the adult rat trigeminal ganglion results from the release of a mitogenic protein from explanted sensory neurons.

Authors:  J Y Wen; C M Morshead; D van der Kooy
Journal:  J Cell Biol       Date:  1994-03       Impact factor: 10.539

6.  A role for TGF-beta in oligodendrocyte differentiation.

Authors:  R D McKinnon; G Piras; J A Ida; M Dubois-Dalcq
Journal:  J Cell Biol       Date:  1993-06       Impact factor: 10.539

  6 in total

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