Growth/differentiation factor-15/macrophage inhibitory cytokine-1 is a novel trophic factor for midbrain dopaminergic neurons in vivo
Transforming growth factor-βs (TGF-βs) constitute an expanding family of multifunctional cytokines with prominent roles in development, cell proliferation, differentiation, and repair. We have cloned, expressed, and raised antibodies against a distant member of the TGF-βs, growth/differentiation fac...
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| Hauptverfasser: | , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
1 December 2000
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| In: |
The journal of neuroscience
Year: 2000, Jahrgang: 20, Heft: 23, Pages: 8597-8603 |
| ISSN: | 1529-2401 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: http://www.jneurosci.org/content/20/23/8597
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| Verfasserangaben: | Jens Strelau, Aideen Sullivan, Martina Böttner, Paul Lingor, Elisabeth Falkenstein, Clemens Suter-Crazzolara, Dagmar Galter, Jozsef Jaszai, Kerstin Krieglstein, and Klaus Unsicker |
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| 245 | 1 | 0 | |a Growth/differentiation factor-15/macrophage inhibitory cytokine-1 is a novel trophic factor for midbrain dopaminergic neurons in vivo |c Jens Strelau, Aideen Sullivan, Martina Böttner, Paul Lingor, Elisabeth Falkenstein, Clemens Suter-Crazzolara, Dagmar Galter, Jozsef Jaszai, Kerstin Krieglstein, and Klaus Unsicker |
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| 500 | |a Von den Autoren angegeben als: "GDF-15/MIC-1 is a novel trophic factor for midbrain dopaminergic neurons in vivo" | ||
| 520 | |a Transforming growth factor-βs (TGF-βs) constitute an expanding family of multifunctional cytokines with prominent roles in development, cell proliferation, differentiation, and repair. We have cloned, expressed, and raised antibodies against a distant member of the TGF-βs, growth/differentiation factor-15 (GDF-15). GDF-15 is identical to macrophage inhibitory cytokine-1 (MIC-1). GDF-15/MIC-1 mRNA and protein are widely distributed in the developing and adult CNS and peripheral nervous systems, including choroid plexus and CSF. GDF-15/MIC-1 is a potent survival promoting and protective factor for cultured and iron-intoxicated dopaminergic (DAergic) neurons cultured from the embryonic rat midbrain floor. The trophic effect of GDF-15/MIC-1 was not accompanied by an increase in cell proliferation and astroglial maturation, suggesting that GDF-15/MIC-1 probably acts directly on neurons. GDF-15/MIC-1 also protects 6-hydroxydopamine (6-OHDA)-lesioned nigrostriatal DAergic neurons in vivo. Unilateral injections of GDF-15/MIC-1 into the medial forebrain bundle just above the substantia nigra (SN) and into the left ventricle (20 μg each) immediately before a 6-OHDA injection (8 μg) prevented 6-OHDA-induced rotational behavior and significantly reduced losses of DAergic neurons in the SN. This protection was evident for at least 1 month. Administration of 5 μg of GDF-15/MIC-1 in the same paradigm also provided significant neuroprotection. GDF-15/MIC-1 also promoted the serotonergic phenotype of cultured raphe neurons but did not support survival of rat motoneurons. Thus, GDF-15/MIC-1 is a novel neurotrophic factor with prominent effects on DAergic and serotonergic neurons. GDF-15/MIC-1 may therefore have a potential for the treatment of Parkinson's disease and disorders of the serotonergic system. | ||
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| 650 | 4 | |a dopaminergic neurons | |
| 650 | 4 | |a GDF-15/MIC-1 | |
| 650 | 4 | |a neurotrophic factor | |
| 650 | 4 | |a Parkinson's disease | |
| 650 | 4 | |a TGF-β | |
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