Poulsen K T, Armanini M P, Klein R D, Hynes M A, Phillips H S, Rosenthal A
Department of Neuroscience, Genentech, Inc., South San Francisco, California 94080.
Neuron. 1994 Nov;13(5):1245-52. doi: 10.1016/0896-6273(94)90062-0.
The vertebrate ventral midbrain contains 3-4 x 10(4) dopaminergic neurons that influence motor activity, emotional behavior, and cognition. Recently, glial cell line-derived neurotrophic factor (GDNF) was shown to be a potent survival factor for these dopaminergic neurons in culture. However, many midbrain dopaminergic neurons project to targets that do not express GDNF. We report here that transforming growth factors (TGFs) TGF beta 2 and TGF beta 3, which are distantly related to GDNF, also prevent the death of cultured rat embryonic midbrain dopaminergic neurons at picomolar concentrations. Furthermore, we find that TGF beta 2, TGF beta 3, and GDNF are expressed sequentially as local and target-derived trophic factors and that subpopulations of dopaminergic neurons projecting to distinct targets have access to only one of these factors. These findings are consistent with the idea that GDNF, TGF beta 2, and TGF beta 3 are physiological survival factors for developing midbrain dopaminergic neurons and may have applications as therapeutics for Parkinson's disease, a neurodegenerative disorder of dopaminergic neurons.
脊椎动物的腹侧中脑含有3 - 4×10⁴个多巴胺能神经元,这些神经元影响运动活动、情绪行为和认知。最近,胶质细胞系源性神经营养因子(GDNF)被证明是培养中这些多巴胺能神经元的一种有效存活因子。然而,许多中脑多巴胺能神经元投射到不表达GDNF的靶点。我们在此报告,与GDNF有远亲关系的转化生长因子(TGFs)TGFβ2和TGFβ3,在皮摩尔浓度下也能防止培养的大鼠胚胎中脑多巴胺能神经元死亡。此外,我们发现TGFβ2、TGFβ3和GDNF作为局部和靶点源性营养因子依次表达,并且投射到不同靶点的多巴胺能神经元亚群只能接触到这些因子中的一种。这些发现与以下观点一致,即GDNF、TGFβ2和TGFβ3是发育中的中脑多巴胺能神经元的生理性存活因子,并且可能作为治疗帕金森病(一种多巴胺能神经元的神经退行性疾病)的疗法应用。