Kure R, Brown I R
Department of Zoology, University of Toronto, Ontario, Canada.
Neurochem Res. 1995 Jul;20(7):833-46. doi: 10.1007/BF00969696.
A regional Northern blot analysis demonstrated that the highest levels of NF-L mRNA in the adult mouse brain are present in brain stem followed by mid-brain, with lower levels found in neocortex, cerebellum, and hippocampus. The study was extended to the cellular level over course of postnatal development using in situ hybridization. This developmental analysis revealed that the expression of NF-L mRNA closely follows the differentiation pattern of many large neurons during postnatal neurogenesis. Neurons which differentiate early such as Purkinje, mitral, pyramidal, and large neurons of brain stem and thalamic nuclei, expressed high levels of NF-L mRNA at postnatal day 1. Early expression of NF-L mRNA may be required for the maintenance of the extensive neurofilament protein networks that are detected within the axons of larger neurons. Smaller neurons which differentiate later, such as dentate gyrus granule cells, small pyramidal and granule cells of the neocortex, and granule cells of the cerebellum, exhibit a delayed expression of NF-L mRNA.
一项区域Northern印迹分析表明,成年小鼠脑中NF-L mRNA水平最高的部位是脑干,其次是中脑,而新皮层、小脑和海马中的水平较低。该研究通过原位杂交在出生后发育过程中扩展到细胞水平。这种发育分析表明,NF-L mRNA的表达与出生后神经发生过程中许多大神经元的分化模式密切相关。早期分化的神经元,如浦肯野细胞、二尖瓣细胞、锥体神经元以及脑干和丘脑核的大神经元,在出生后第1天表达高水平的NF-L mRNA。NF-L mRNA的早期表达可能是维持在较大神经元轴突内检测到的广泛神经丝蛋白网络所必需的。后期分化的较小神经元,如齿状回颗粒细胞、新皮层的小锥体和颗粒细胞以及小脑颗粒细胞,表现出NF-L mRNA的延迟表达。