Burbach J Peter H, Smits Simone, Smidt Marten P
Rudolf Magnus Institute of Neuroscience, Department of Pharmacology and Anatomy, University Medical Center Utrecht, Utrecht, The Netherlands.
Ann N Y Acad Sci. 2003 Jun;991:61-8. doi: 10.1111/j.1749-6632.2003.tb07463.x.
The development of midbrain dopamine (DA) neurons follows a number of stages marked by distinct events. After preparation of the region by signals that provide induction and patterning, at least two cascades of transcription factors contribute to the fully matured midbrain DA systems. One cascade involving the nuclear receptor Nurr1 is required to synthesize the neurotransmitter DA; the enzyme tyrosine hydroxylase (TH) depends on it. The other cascade involves homeobox genes. Lmx1b and engrailed genes are expressed before the genesis of DA neurons and maintain their expression in these neurons. Lmx1b drives Ptx3, which is the latest transcription factor known to be induced. Its induction coincides with that of TH. Disruption of the function of Ptx3 affects the formation of the substantia nigra (SN) and alters the anatomical organization of the midbrain DA systems. While each cascade contributes to a specific aspect of DA neurons, both cascades are required for survival during development, indicating that the maintenance of DA neurons is delicately dependent on the appropriate activity of multiple transcriptional cascades.
中脑多巴胺(DA)神经元的发育遵循多个以不同事件为标志的阶段。在通过提供诱导和模式化的信号对该区域进行准备之后,至少有两个转录因子级联反应有助于中脑DA系统完全成熟。一个涉及核受体Nurr1的级联反应是合成神经递质DA所必需的;酶酪氨酸羟化酶(TH)依赖于它。另一个级联反应涉及同源盒基因。Lmx1b和engrailed基因在DA神经元产生之前就已表达,并在这些神经元中维持其表达。Lmx1b驱动Ptx3,Ptx3是已知被诱导的最新转录因子。它的诱导与TH的诱导同时发生。Ptx3功能的破坏会影响黑质(SN)的形成,并改变中脑DA系统的解剖结构。虽然每个级联反应都对DA神经元的特定方面有贡献,但两个级联反应在发育过程中对生存都是必需的,这表明DA神经元的维持微妙地依赖于多个转录级联反应的适当活动。