Department of Neuromorphology, Max-Planck-Institute for Psychiatry, D-8033 Martinsried (FRG).
Restor Neurol Neurosci. 1992 Jan 1;4(2):107-15. doi: 10.3233/RNN-1992-4203.
Calcitonin-gene related peptide (CGRP) is a neuromodulatory peptide present in motoneurons and a subpopulation of sensory neurons of the adult peripheral nervous system. Here we have investigated the changes in axonal transport of CGRP and CGRP receptor expression in the injured and regenerating rat sciatic nerve using CGRP-immunocytochemistry, radioimmunoassay and quantitative in situ receptor autoradiography techniques. Axotomy led to a gradual and prolonged, 2.5- to 3.5-fold increase in specific CGRP binding to the distal part of the crushed sciatic nerve, beginning 4-6 days after axotomy. An even stronger, up to 30-fold increase was observed after 30-42 day denervation in the distal part of the transected sciatic nerve, where neurite reinnervation was prevented by retroversion and ligation of the proximal nerve stump. Reconnection of the proximal and distal nerve stumps 21 days after transection did not lead to a major reduction in specific CGRP binding but prevented a further increase that occurred between 21 and 42 days after transection without reconnection. In contrast, the anterograde axonal transport of CGRP decreased after axotomy to 40-50% of the control values 6-8 days after nerve crush but recovered towards normal levels during successful regeneration. Interestingly, the retrograde axonal transport of CGRP appeared to amount to only 10-20% of the anterograde transport, suggesting that the peptide may be released by the regenerating neurites into the endoneurium of the injured peripheral nerve. In view of the persistent upregulation in endoneural CGRP binding after axotomy these data indicate that axonal CGRP could play a regulatory role in mediating axonal-endoneural cell interaction during peripheral nerve regeneration.
降钙素基因相关肽(CGRP)是一种存在于运动神经元和成年周围神经系统感觉神经元中的神经调节肽。在这里,我们使用 CGRP 免疫细胞化学、放射免疫测定和定量原位受体放射自显影技术研究了损伤和再生大鼠坐骨神经中 CGRP 和 CGRP 受体表达的轴突运输变化。轴突切断导致特异性 CGRP 与粉碎的坐骨神经远端结合的逐渐和延长的 2.5-3.5 倍增加,从轴突切断后 4-6 天开始。在切断的坐骨神经远端观察到甚至更强的,高达 30 倍的增加,在 30-42 天去神经后,通过反转和结扎近端神经残端防止了神经突再支配。在切断后 21 天重新连接近端和远端神经残端不会导致特异性 CGRP 结合的大幅减少,但会防止在没有重新连接的情况下在切断后 21 天至 42 天之间发生的进一步增加。相比之下,轴突切断后 CGRP 的顺行轴突运输减少到神经挤压后 6-8 天的对照值的 40-50%,但在成功再生期间恢复到正常水平。有趣的是,CGRP 的逆行轴突运输似乎仅占顺行运输的 10-20%,表明该肽可能通过再生的神经突释放到损伤的周围神经的神经内膜中。鉴于轴突切断后神经内膜 CGRP 结合的持续上调,这些数据表明轴突 CGRP 在介导周围神经再生过程中的轴突-神经内膜细胞相互作用中可能发挥调节作用。