Padilla S, Freeman E B, Tandon P, Wilson V Z
Cellular and Molecular Toxicology Branch, U.S. Environmental Protection Agency, Chapel Hill, North Carolina 27711.
J Neurochem. 1993 May;60(5):1900-5. doi: 10.1111/j.1471-4159.1993.tb13418.x.
Retrograde axonal transport of phosphatidylcholine in the sciatic nerve has been demonstrated only after injection of lipid precursors into the cell body region. We now report, however, that after microinjection (1 microliter) of [methyl-3H]choline chloride into the rat sciatic nerve (35-40 mm distal to the L4 and L5 dorsal root ganglia), time-dependent accumulation of 3H-labeled material occurred in dorsal root ganglia ipsilateral, but not contralateral, to the injection site. The level of radioactivity in the ipsilateral dorsal root ganglia was minimal at 2 h after isotope injection but was significantly increased at 7, 24, 48, and 72 h after intraneural isotope injection (n = 3-8 per time point); at these time points, all of the radiolabel in the chloroform/methanol extract of the ipsilateral dorsal root ganglia was present in phosphatidylcholine. The radioactivity in the water-soluble fraction did not show a time-dependent accumulation in the ipsilateral dorsal root ganglia as compared with the contralateral DRGs, ruling out transport or diffusion of precursor molecules. In addition, colchicine injection into the sciatic nerve proximal to the isotope injection site prevented the accumulation of radiolabel in the ipsilateral dorsal root ganglia. Therefore, this time-dependent accumulation of radiolabeled phosphatidylcholine in the ipsilateral dorsal root ganglia is most likely due to retrograde axonal transport of locally synthesized phospholipid material. Moreover, 24 h after injection of both [3H]choline and [35S]-methionine into the sciatic nerve, the ipsilateral/contralateral ratio of radiolabel was 11.7 for 3H but only 1.1 for 35S, indicating that only locally synthesized choline phospholipids, but not protein, were retrogradely transported.
仅在将脂质前体注射到细胞体区域后,才证明了坐骨神经中磷脂酰胆碱的逆行轴突运输。然而,我们现在报告,在将[甲基 - 3H]氯化胆碱微量注射(1微升)到大鼠坐骨神经(L4和L5背根神经节远端35 - 40毫米处)后,注射部位同侧而非对侧的背根神经节中出现了3H标记物质的时间依赖性积累。同位素注射后2小时,同侧背根神经节中的放射性水平最低,但在神经内注射同位素后7、24、48和72小时显著增加(每个时间点n = 3 - 8);在这些时间点,同侧背根神经节氯仿/甲醇提取物中的所有放射性标记物都存在于磷脂酰胆碱中。与对侧背根神经节相比,同侧背根神经节水溶性部分的放射性没有显示出时间依赖性积累,排除了前体分子的运输或扩散。此外,在同位素注射部位近端的坐骨神经中注射秋水仙碱可阻止同侧背根神经节中放射性标记物的积累。因此,同侧背根神经节中放射性标记的磷脂酰胆碱的这种时间依赖性积累很可能是由于局部合成的磷脂物质的逆行轴突运输。此外,在将[3H]胆碱和[35S] - 甲硫氨酸都注射到坐骨神经中24小时后,3H的放射性标记同侧/对侧比率为11.7,而35S仅为1.1,这表明只有局部合成的胆碱磷脂被逆行运输,而蛋白质没有。