Department of Anatomy, University of Helsinki, 00014 Helsinki, Finland.
Department of Anatomy, University of Helsinki, 00014 Helsinki, Finland
J Neurosci. 2020 Aug 5;40(32):6146-6164. doi: 10.1523/JNEUROSCI.2636-19.2020. Epub 2020 Jul 6.
Cerebral dopamine neurotrophic factor (CDNF) protects dopaminergic neurons against toxic damage in the rodent brain and is in clinical trials to treat Parkinson's disease patients. Yet the underlying mechanism is poorly understood. To examine its significance for neural circuits and behavior, we examined the development of neurotransmitter systems from larval to male adult mutant zebrafish lacking Although a lack of did not affect overall brain dopamine levels, dopaminergic neuronal clusters showed significant abnormalities. The number of histamine neurons that surround the dopaminergic neurons was significantly reduced. Expression of in the brain was elevated in mutants throughout their lifespan. There were abnormally few GABA neurons in the hypothalamus in the mutant larvae, and expression of glutamate decarboxylase was reduced throughout the brain. mutant adults showed a range of behavioral phenotypes, including increased sensitivity to pentylenetetrazole-induced seizures. Shoaling behavior of mutant adults was abnormal, and they did not display social attraction to conspecifics. CDNF plays a profound role in shaping the neurotransmitter circuit structure, seizure susceptibility, and complex behaviors in zebrafish. These findings are informative for dissecting the diverse functions of this poorly understood factor in human conditions related to Parkinson's disease and complex behaviors. A zebrafish lacking cdnf grows normally and shows no overt morphologic phenotype throughout the life span. Remarkably, impaired social cohesion and increased seizure susceptibility were found in adult KO fish conceivably associated with significant changes of dopaminergic, GABAergic, and histaminergic systems in selective brain areas. These findings suggest that cdnf has broad effects on regulating neurogenesis and maturation of transmitter-specific neuronal types during development and throughout adulthood, rather than ones restricted to the dopaminergic systems.
脑源性神经营养因子 (CDNF) 可保护啮齿动物大脑中的多巴胺能神经元免受毒性损伤,并且正处于临床试验阶段,以治疗帕金森病患者。然而,其潜在机制尚不清楚。为了研究其对神经回路和行为的意义,我们检查了缺乏 的幼鱼到雄性成年突变斑马鱼的神经递质系统的发育情况。尽管缺乏 并不影响大脑多巴胺的总体水平,但多巴胺能神经元簇显示出明显的异常。围绕多巴胺能神经元的组胺神经元数量显著减少。在整个生命周期中, 突变体大脑中的 表达升高。突变体幼虫下丘脑的 GABA 神经元数量异常少,整个大脑中的谷氨酸脱羧酶表达减少。 突变体成年鱼表现出多种行为表型,包括对戊四氮诱导的癫痫发作的敏感性增加。突变体成年鱼的聚群行为异常,它们对同种的社交吸引力降低。CDNF 在塑造斑马鱼的神经递质回路结构、癫痫易感性和复杂行为方面发挥着深远的作用。这些发现为解析该因素在与帕金森病和复杂行为相关的人类疾病中的多种功能提供了信息。缺乏 cdnf 的斑马鱼在整个生命周期内正常生长,没有明显的形态表型。值得注意的是,在成年 KO 鱼中发现了社交凝聚力受损和癫痫易感性增加,这可能与选择性大脑区域中多巴胺能、GABA 能和组胺能系统的显著变化有关。这些发现表明,cdnf 对调节神经发生和发育过程中特定神经递质类型的成熟具有广泛的影响,而不仅仅局限于多巴胺能系统。