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Interferon-γ, tumor necrosis factor-α, and transforming growth factor-β inhibit cyclic AMP-induced Schwann cell differentiation

✍ Scribed by Robert P. Lisak; Beverly Bealmear; Joyce A. Benjamins; Anne M. Skoff


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
300 KB
Volume
36
Category
Article
ISSN
0894-1491

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✦ Synopsis


Abstract

Schwann cells differentiate in vivo in response to contact with axons, and cAMP simulates some of these aspects of differentiation in vitro, particularly morphologic changes and expression of certain phenotypic molecules. Unfractionated inflammatory cytokines inhibit cAMP‐induced Schwann cell expression of galactolipids (Gal). We sought to identify which cytokines were responsible for this inhibition and to determine whether other phenotypic indicators of Schwann cell differentiation were also affected. Neonatal rat Schwann cells were incubated in vitro with 1 mM 8 Bromo cAMP (8 Br cAMP) with or without the addition of interleukin‐1α (IL‐1α), IL‐1β, IL‐2, IL‐6, tumor necrosis factor‐α (TNF‐α), interferon‐γ (IFN‐γ), or transforming growth factor‐β (TGF‐β). Cells were then examined for morphologic changes and for expression of surface Gal and low‐affinity nerve growth factor receptor (NGFRp75), employing indirect immunofluorescence. 8 Br cAMP induced Schwann cell upregulation of Gal, downregulation of NGFRp75, and the cells became enlarged and somewhat amorphous and irregular in appearance. Cells treated with IFN‐γ or TNF‐α alone were more bipolar and more evenly distributed on coverslips than were control cells, whereas TGF‐β alone induced elongated cells often in a swirling pattern. None of the cytokines alone induced upregulation of Gal or downregulation of NGFRp75. TNF‐α, IFN‐γ, and TGF‐β inhibited the 8 Br cAMP‐induced morphologic changes, as well as the upregulation of Gal and downregulation of NGFRp75. The other cytokines had no effects on Gal or NGFRp75 expression. Thus, these three cytokines, which are present in inflammatory lesions in the peripheral nervous system, are capable of inhibiting Schwann cell differentiation. GLIA 36:354–363, 2001. © 2001 Wiley‐Liss, Inc.


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