Stoeckel K, Schwab M, Thoenen H
Brain Res. 1975 May 16;89(1):1-14. doi: 10.1016/0006-8993(75)90129-8.
In previous studies it has been shown that nerve growth factor (NGF) is taken up with a high selectivity by adrenergic nerve terminals and is transported retrogradely to the perikaryon11,22. It was the aim of the present experiments to investigate whether the sensory neurons exhibit the same high degree of selectivity for retrograde transport throughout the whole life cycle, although it is known that their dramatic response to NGF is confined to a short period of ontogenetic development. Unilateral injection of [125I]NGF into the forepaw of adult rats was followed by a preferential accumulation of radioactivity in the sensory ganglia (C6-C7) of the injected side. However, this preferential accumulation was not detectable earlier than 6 h after injection and reached a maximum (ratio between injected and non-injected side, 5:1) after 11-16 h. Transection of the plexus brachialis abolished and local administration of colchicine prior to that of [125I]NGF greatly reduced the preferential accumulation of radioactivity in the ganglia of the injected side. The rate of retrograde transport of NGF in sensory neurons was calculated to be 13 mm/h which is about 5 times faster than that in adrenergic neurons. The selectivity of this retrograde transport was demonstrated by the fact that injection of 125I-labeled bovine serum albumin and cytochrome c did not result in a preferential accumulation of radioactivity in the sensory ganglia of the injected side. Light microscopic autoradiography revealed heavily labeled cells in the sensory ganglia (C6-C7) of the injected side after administration of [125I]NGF into the forepaw. Only cells belonging to the large cell type were labeled. Prolonged (7 mug/g/day over 5 days) injection of NGF into the forepaw of 10-day-old rats did not result in a hypertropic response of the sensory neurons as far as can be judged from morphometric studies at the light microscopic level.
在先前的研究中已经表明,神经生长因子(NGF)被肾上腺素能神经末梢高度选择性地摄取,并逆向运输至胞体11,22。本实验的目的是研究感觉神经元在整个生命周期中是否对逆向运输表现出相同程度的高度选择性,尽管已知它们对NGF的显著反应仅限于个体发育的短时期。将[125I]NGF单侧注射到成年大鼠的前爪后,注射侧的感觉神经节(C6 - C7)中出现放射性的优先积累。然而,这种优先积累在注射后6小时之前无法检测到,在11 - 16小时后达到最大值(注射侧与未注射侧的比值为5:1)。臂丛神经横断消除了这种现象,并且在注射[125I]NGF之前局部给予秋水仙碱大大降低了注射侧神经节中放射性的优先积累。计算出NGF在感觉神经元中的逆向运输速率为13毫米/小时,这比在肾上腺素能神经元中的运输速率快约5倍。这种逆向运输的选择性通过以下事实得以证明:注射125I标记的牛血清白蛋白和细胞色素c并未导致注射侧感觉神经节中放射性的优先积累。光学显微镜放射自显影显示,在前爪注射[125I]NGF后,注射侧的感觉神经节(C6 - C7)中有大量标记细胞。只有属于大细胞类型的细胞被标记。从光学显微镜水平的形态计量学研究判断,向10日龄大鼠的前爪长期(5天内每天7微克/克)注射NGF并未导致感觉神经元出现肥大反应。