LaVail J H, Sugino I K
Brain Res. 1984 Jun 18;304(1):59-69. doi: 10.1016/0006-8993(84)90861-8.
We have studied the subcellular localization of peroxidase-labeled organelles after anterograde axonal transport by chick retinal ganglion cells that had been exposed 23-25 h earlier to wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP). After intravitreal injection of WGA-HRP, we found in the optic tectum that 82% of labeled organelles were located within axons and axon terminals. The organelles included: tubules and cisternae of the smooth endoplasmic reticulum, hypolemmal cisternae, vesicles, dense bodies and multivesticular bodies. We also measured the distances between the centers of the labeled organelles and the plasma membrane of these profiles. The density of organelles (number of organelles/micron 2) was plotted as a function of distance from the plasma membrane. Irrespective of the dose of lectin-peroxidase injected, labeled organelles were most densely concentrated in a 30 nm wide annular zone centered 75 nm in from the plasma membrane. In axon terminals the labeled organelles were most concentrated 75-90 nm in from the plasma membrane. Assuming that the peroxidase label indicates the presence of WGA-HRP, we conclude that after anterograde axonal transport the lectin accumulates in lysosomal organelles and elements of the smooth endoplasmic reticulum. Therefore, in contrast to the more restricted localization of [125I]WGA as inferred from electron microscopic autoradiography after uptake and transport by the same cell type, WGA-HRP-labeled organelles are found more diffusely within the axoplasm, particularly in axon terminals. Furthermore, peroxidase-labeled organelles in dendritic, glial or neuronal cell bodies in the tectum were seen less frequently than expected based on evidence of frequent transfer to second cells after intravitreal injections of [125I]WGA. Thus, we infer that at these concentrations WGA labeled with HRP may not be transferred intercellularly as efficiently as even lower concentrations of iodinated WGA are apparently transferred.
我们研究了鸡视网膜神经节细胞顺行轴突运输后,过氧化物酶标记细胞器的亚细胞定位。这些细胞在23 - 25小时前暴露于与辣根过氧化物酶偶联的麦胚凝集素(WGA - HRP)。玻璃体内注射WGA - HRP后,我们在视顶盖中发现82%的标记细胞器位于轴突和轴突终末内。这些细胞器包括:滑面内质网的小管和潴泡、质膜下潴泡、小泡、致密体和多囊体。我们还测量了标记细胞器中心与这些轮廓的质膜之间的距离。将细胞器密度(细胞器数量/平方微米)绘制为距质膜距离的函数。无论注射的凝集素 - 过氧化物酶剂量如何,标记细胞器最密集地集中在距质膜75纳米处中心宽30纳米的环形区域内。在轴突终末,标记细胞器最集中在距质膜75 - 90纳米处。假设过氧化物酶标记表明WGA - HRP的存在,我们得出结论,顺行轴突运输后凝集素积聚在溶酶体细胞器和滑面内质网成分中。因此,与通过相同细胞类型摄取和运输后电子显微镜放射自显影推断的[125I]WGA更局限的定位相反,WGA - HRP标记的细胞器在轴质内分布更分散,尤其是在轴突终末。此外,基于玻璃体内注射[125I]WGA后频繁转移到第二个细胞的证据,视顶盖中树突、胶质或神经元细胞体中的过氧化物酶标记细胞器比预期的少见。因此,我们推断在这些浓度下,用HRP标记的WGA可能不像甚至更低浓度的碘化WGA那样有效地在细胞间转移。