Strelau J, Schober A, Sullivan A, Schilling L, Unsicker K
Neuroanatomy and Interdisciplinary Center for Neurosciences (IZN), University of Heidelberg, Germany.
J Neural Transm Suppl. 2003(65):197-203. doi: 10.1007/978-3-7091-0643-3_12.
This review summarizes the evidence that GDF-15, a recently discovered member of the TGF-beta superfamily, is a trophic factor for nigral dopamine neurons, both in vitro and in vivo. Specifically, GDF-15 promotes survival and differentiation of embryonic rat dopaminergic neurons, but not of other neuron populations, with the exception of serotonergic raphe neurons. The neurotrophic effect of GDF-15 seems to be direct and not mediated through glial cells. In the rat 6-hydroxydopamine model of parkinsonism GDF-15 rescues intoxicated dopaminergic neurons and abolishes abnormal turning behavior. The most prominent site of synthesis of GDF-15 within the brain is the choroid plexus, which secretes GDF-15 into the cerebrospinal fluid, from where the molecule can penetrate through the ependymal layer into the parenchyma. Analysis of mouse mutants lacking GDF-15 will reveal whether the endogenous factor also has a role in promoting embryonic and protecting lesioned nigral dopamine neurons.
生长分化因子15(GDF - 15)是转化生长因子β(TGF - β)超家族最近发现的成员,在体外和体内均为黑质多巴胺能神经元的营养因子。具体而言,GDF - 15可促进胚胎大鼠多巴胺能神经元的存活和分化,但除了血清素能中缝神经元外,对其他神经元群体无此作用。GDF - 15的神经营养作用似乎是直接的,并非通过胶质细胞介导。在大鼠帕金森病6 - 羟基多巴胺模型中,GDF - 15可挽救中毒的多巴胺能神经元并消除异常旋转行为。脑内GDF - 15最主要的合成部位是脉络丛,其将GDF - 15分泌到脑脊液中,该分子可从脑脊液穿过室管膜层进入脑实质。对缺乏GDF - 15的小鼠突变体进行分析,将揭示内源性因子是否在促进胚胎黑质多巴胺能神经元生长及保护受损神经元方面也发挥作用。