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转化生长因子-β超家族成员生长/分化因子5对中脑多巴胺能神经元的营养和保护作用。

Trophic and protective effects of growth/differentiation factor 5, a member of the transforming growth factor-beta superfamily, on midbrain dopaminergic neurons.

作者信息

Krieglstein K, Suter-Crazzolara C, Hötten G, Pohl J, Unsicker K

机构信息

Department of Anatomy and Cell Biology, University of Heidelberg, Germany.

出版信息

J Neurosci Res. 1995 Dec;42(5):724-32. doi: 10.1002/jnr.490420516.

Abstract

Growth/differentiation factor 5 (GDF5) is a novel member of the transforming growth factor-beta (TGF-beta) superfamily of multifunctional cytokines. We show here that GDF5 is expresed in the developing CNS including the mesencephalon and acts as a neurotrophic, survival promoting molecule for rat dopaminergic midbrain neurons, which degenerate in Parkinson's disease. Recombinant human GDF5 supports dopaminergic neurons, dissected at embryonic day (E) 14 and cultured for 8 days under serum-free conditions, to almost the same extent as TGF-beta 3, and is as effective as glial cell line-derived neurotrophic factor (GDNF), two established trophic factors for midbrain dopaminergic neurons. In contrast to TGF-beta and GDNF, GDF5 augments numbers of astroglial cells in the cultures, suggesting that it may act indirectly and through pathways different from those triggered by TGF-beta and GDNF. GDF5 also protects dopaminergic neurons against the toxicity of N-methylpyridinium ion (MPP+), which selectively damages dopaminergic neurons through mechanisms currently debated in the etiology of Parkinson's disease (PD). GDF5 may therefore now be tested in animal models of PD and might become useful in the treatment of PD.

摘要

生长/分化因子5(GDF5)是多功能细胞因子转化生长因子-β(TGF-β)超家族的一个新成员。我们在此表明,GDF5在包括中脑在内的发育中的中枢神经系统中表达,并作为一种神经营养、促进存活的分子作用于大鼠多巴胺能中脑神经元,这些神经元在帕金森病中会退化。重组人GDF5对在胚胎第14天(E14)分离并在无血清条件下培养8天的多巴胺能神经元的支持程度,几乎与TGF-β3相同,并且与胶质细胞系衍生的神经营养因子(GDNF)一样有效,GDNF是两种已确定的中脑多巴胺能神经元的营养因子。与TGF-β和GDNF不同,GDF5增加了培养物中星形胶质细胞的数量,这表明它可能通过与TGF-β和GDNF触发的途径不同的途径间接发挥作用。GDF5还能保护多巴胺能神经元免受N-甲基吡啶离子(MPP+)的毒性影响,MPP+通过目前在帕金森病(PD)病因学中存在争议的机制选择性地损害多巴胺能神经元。因此,现在可以在PD动物模型中对GDF5进行测试,它可能在PD治疗中发挥作用。

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