Goulding Susan R, Anantha Jayanth, Collins Louise M, Sullivan Aideen M, O'Keeffe Gerard W
Department of Anatomy and Neuroscience, and Cork Neuroscience Centre, University College Cork, Cork, Ireland.
Department of Anatomy and Neuroscience, and Cork Neuroscience Centre; Department of Physiology, University College Cork, Cork, Ireland.
Neural Regen Res. 2022 Jan;17(1):38-44. doi: 10.4103/1673-5374.314290.
Parkinson's disease is the most common movement disorder worldwide, affecting over 6 million people. It is an age-related disease, occurring in 1% of people over the age of 60, and 3% of the population over 80 years. The disease is characterized by the progressive loss of midbrain dopaminergic neurons from the substantia nigra, and their axons, which innervate the striatum, resulting in the characteristic motor and non-motor symptoms of Parkinson's disease. This is paralleled by the intracellular accumulation of α-synuclein in several regions of the nervous system. Current therapies are solely symptomatic and do not stop or slow disease progression. One promising disease-modifying strategy to arrest the loss of dopaminergic neurons is the targeted delivery of neurotrophic factors to the substantia nigra or striatum, to protect the remaining dopaminergic neurons of the nigrostriatal pathway. However, clinical trials of two well-established neurotrophic factors, glial cell line-derived neurotrophic factor and neurturin, have failed to meet their primary end-points. This failure is thought to be at least partly due to the downregulation by α-synuclein of Ret, the common co-receptor of glial cell line-derived neurorophic factor and neurturin. Growth/differentiation factor 5 is a member of the bone morphogenetic protein family of neurotrophic factors, that signals through the Ret-independent canonical Smad signaling pathway. Here, we review the evidence for the neurotrophic potential of growth/differentiation factor 5 in in vitro and in vivo models of Parkinson's disease. We discuss new work on growth/differentiation factor 5's mechanisms of action, as well as data showing that viral delivery of growth/differentiation factor 5 to the substantia nigra is neuroprotective in the α-synuclein rat model of Parkinson's disease. These data highlight the potential for growth/differentiation factor 5 as a disease-modifying therapy for Parkinson's disease.
帕金森病是全球最常见的运动障碍疾病,影响着超过600万人。它是一种与年龄相关的疾病,在60岁以上的人群中发病率为1%,在80岁以上的人群中发病率为3%。该疾病的特征是中脑黑质多巴胺能神经元及其支配纹状体的轴突逐渐丧失,导致帕金森病典型的运动和非运动症状。与此同时,α-突触核蛋白在神经系统的多个区域细胞内积聚。目前的治疗方法仅仅是对症治疗,无法阻止或减缓疾病进展。一种有前景的疾病修饰策略是将神经营养因子靶向递送至黑质或纹状体,以保护黑质纹状体通路中剩余的多巴胺能神经元,从而阻止多巴胺能神经元的丧失。然而,两种成熟的神经营养因子——胶质细胞源性神经营养因子和神经营养素的临床试验均未达到其主要终点。这种失败至少部分归因于α-突触核蛋白对胶质细胞源性神经营养因子和神经营养素的共同共受体Ret的下调。生长/分化因子5是神经营养因子骨形态发生蛋白家族的成员,通过不依赖Ret的经典Smad信号通路发挥作用。在此,我们综述了生长/分化因子5在帕金森病体外和体内模型中神经营养潜力的证据。我们讨论了关于生长/分化因子5作用机制的新研究,以及表明将生长/分化因子5通过病毒递送至黑质在帕金森病α-突触核蛋白大鼠模型中具有神经保护作用的数据。这些数据突出了生长/分化因子5作为帕金森病疾病修饰疗法的潜力。