Curtis R, Adryan K M, Stark J L, Park J S, Compton D L, Weskamp G, Huber L J, Chao M V, Jaenisch R, Lee K F
Regeneron Pharmaceuticals, Inc., Tarrytown, New York 10591, USA.
Neuron. 1995 Jun;14(6):1201-11. doi: 10.1016/0896-6273(95)90267-8.
The receptor mechanisms mediating the retrograde axonal transport of the neurotrophins have been investigated in adult rats. We show that transport of the TrkB ligands NT-4 and BDNF to peripheral neurons is dependent on the low affinity neurotrophin receptor (LNR). Pharmacological manipulation of LNR in vivo using either an anti-LNR antibody or a soluble recombinant LNR extracellular domain completely blocked retrograde transport of NT-4 and BDNF to sensory neurons, while having minimal effects on the transport of NGF in either sensory or sympathetic neurons. Furthermore, in mice with a null mutation of LNR, the transport of NT-4 and BDNF, but not NGF, was dramatically reduced. These observations demonstrate a selective role for LNR in retrograde transport of the various neurotrophins from distinct target regions in vivo.
在成年大鼠中研究了介导神经营养因子逆行轴突运输的受体机制。我们发现,TrkB配体NT-4和BDNF向周围神经元的运输依赖于低亲和力神经营养因子受体(LNR)。使用抗LNR抗体或可溶性重组LNR细胞外结构域在体内对LNR进行药理学操作,完全阻断了NT-4和BDNF向感觉神经元的逆行运输,而对NGF在感觉神经元或交感神经元中的运输影响最小。此外,在LNR基因敲除的小鼠中,NT-4和BDNF的运输显著减少,但NGF的运输未受影响。这些观察结果表明,LNR在体内不同靶区域的各种神经营养因子逆行运输中具有选择性作用。