Walter I B
Institut d'Histologie et d'Embryologie, Faculté de Médecine, Université de Lausanne, Switzerland.
Eur J Neurosci. 1996 Mar;8(3):455-66. doi: 10.1111/j.1460-9568.1996.tb01229.x.
Apart from several growth factors which play a crucial role in the survival and development of the central and peripheral nervous systems, thyroid hormones can affect different processes involved in the differentiation and maturation of neurons. The present study was initiated to determine whether triiodothyronine (T3) affects the survival and neurite outgrowth of primary sensory neurons in vitro. Dorsal root ganglia (DRG) from 19-day-old embryos or newborn rats were plated in explant or dissociated cell cultures. The effect of T3 on neuron survival was tested, either in mixed DRG cell cultures, where neurons grow with non-neuronal cells, or in neuron-enriched cultures where non-neuronal cells were eliminated at the outset. T3, in physiological concentrations, promoted the growth of neurons in mixed DRG cell cultures as well as in neuron-enriched cultures without added nerve growth factor (NGF). Since neuron survival in neuron-enriched cultures cannot be promoted by endogenous neurotrophic factors synthesized by non-neuronal cells, the increased number of surviving neurons was due to a direct trophic action of T3. Another trophic effect was revealed in this study: T3 sustained the neurite outgrowth of sensory neurons in DRG explants. The stimulatory effect of T3 on nerve fibre outgrowth was considerably reduced when non-neuronal cell proliferation was inhibited by the antimitotic agent cytosine arabinoside, and was completely suppressed when the great majority of non-neuronal cells were eliminated in neuron-enriched cultures. These results indicate that the stimulatory effect of T3 on neurite outgrowth is mediated through non-neuronal cells. It is conceivable that T3 up-regulates Schwann cell expression of a neurotrophic factor, which in turn stimulates axon growth of sensory neurons. Together, these results demonstrate that T3 promotes both survival and neurite outgrowth of primary sensory neurons in DRG cell cultures. The trophic actions of T3 on neuron survival and neurite outgrowth operate under two different pathways.
除了几种在中枢和外周神经系统的存活和发育中起关键作用的生长因子外,甲状腺激素还可影响神经元分化和成熟过程中的不同环节。本研究旨在确定三碘甲状腺原氨酸(T3)是否在体外影响初级感觉神经元的存活和神经突生长。将19日龄胚胎或新生大鼠的背根神经节(DRG)接种于外植体或解离细胞培养物中。在混合DRG细胞培养物(神经元与非神经元细胞一起生长)或富含神经元的培养物(一开始就去除了非神经元细胞)中测试T3对神经元存活的影响。生理浓度的T3在不添加神经生长因子(NGF)的情况下,促进了混合DRG细胞培养物以及富含神经元的培养物中神经元的生长。由于富含神经元的培养物中的神经元存活不能由非神经元细胞合成的内源性神经营养因子促进,因此存活神经元数量的增加是由于T3的直接营养作用。本研究还揭示了另一种营养作用:T3维持了DRG外植体中感觉神经元的神经突生长。当抗有丝分裂剂阿糖胞苷抑制非神经元细胞增殖时,T3对神经纤维生长的刺激作用大大降低,而当富含神经元的培养物中绝大多数非神经元细胞被去除时,T3的刺激作用则完全被抑制。这些结果表明,T3对神经突生长的刺激作用是通过非神经元细胞介导的。可以设想,T3上调了雪旺细胞神经营养因子的表达,进而刺激感觉神经元的轴突生长。总之,这些结果表明,T3促进了DRG细胞培养物中初级感觉神经元的存活和神经突生长。T3对神经元存活和神经突生长的营养作用通过两种不同的途径发挥作用。