Ma J, Yang S X, Ho G J, Festoff B W
Neurobiology Research Lab (151R), VA Medical Center, Kansas City, MO 64128.
Neurochem Res. 1994 Nov;19(11):1363-8. doi: 10.1007/BF00972464.
In a previous study, we localized insulin-like growth factor binding protein 1 (IGFBP-1) to mouse neuromuscular junctions, and intramuscular nerves. To determine if pre-synaptic accumulation of IGFBP-1 occurred, we used double ligation of sciatic nerve in adult mice at different time points. IGFBPs were detected by Western ligand blot (WLB) with 125I-IGF-I. WLB and Western immunoblot (WIB) analysis of extracts from double-ligated nerves showed a delayed (6 days) increase of IGFBP-1 in the soluble fraction between the ligatures and distal to the distal ligature. For comparison we evaluated transport of neurofilament components, using WIB and confirmed the primarily anterograde transport of these intraaxonal proteins. These data suggest that expression of IGFBP-1 is both by activated Schwann cells as well as retrograde axonal transport with likely entry into the axon at the synapse.
在之前的一项研究中,我们将胰岛素样生长因子结合蛋白1(IGFBP-1)定位到小鼠神经肌肉接头和肌内神经。为了确定IGFBP-1是否在突触前积累,我们在成年小鼠的不同时间点对坐骨神经进行了双重结扎。通过用125I-IGF-I进行Western配体印迹(WLB)检测IGFBPs。对双重结扎神经提取物的WLB和Western免疫印迹(WIB)分析显示,结扎之间和远端结扎远端的可溶性部分中IGFBP-1延迟(6天)增加。为了进行比较,我们使用WIB评估了神经丝成分的运输,并证实了这些轴突内蛋白质主要是顺向运输。这些数据表明,IGFBP-1的表达既来自活化的施万细胞,也来自逆行轴突运输,可能在突触处进入轴突。