Cancalon P
Brain Res. 1979 Jan 26;161(1):115-30. doi: 10.1016/0006-8993(79)90199-9.
In the garfish olfactory nerve proteins labeled with [3H]leucine are transported by slow axonal flow as a well-defined crest of radioactivity. At 21 degrees C slow flow moves along the axon with a velocity of 0.92 +/- 0.02 mm/day. It has been possible to analyze 4 subcellular fractions (soluble, mitochondrial and 2 membranous) as well as their polypeptide composition, in areas of the nerve containing (1) the slow moving crest, (2) the material remaining in the nerve behind the crest, and (3) the labeling present in front of the slow crest. Analyses were done 70 and 110 days after isotope deposition. The crest of slow moving radioactivity is characterized by a close parallelism between labeling and protein concentration in the subcellular fractions as well as among the polypeptides constituting these fractions. The radioactivity is mainly associated with mol. wt. of 14,000, 30-45,000, 58,000 and 68,000. This last peak corresponds to a protein not labeled by fast transport, present only in the light membranous fraction. The composition of the moving crest remains essentially constant during the 40-day period investigated. Most of the slow-moving molecules remain in the axon behind the moving crest. This deposited material appears to be redistributed and/or to be turning over more rapidly than the molecules still moving in the crest. A large amount of radioactivity was recovered in front of the moving crest. This might be produced by molecules deposited by fast transport and by material released from the cell body at rates intermediate between the fast and slow phases of transport. The subcellular and polypeptide compositions of this area of the nerve remain constant and are intermediate between the compositions of fast and slow flow. The slowly transported labeled polypeptides in the mitochondrial fraction are of low molecular weight, and were found to be similar in the various areas of the nerve and at the two time points studied, and were even similar to the polypeptide distribution determined for fast transport.
在长吻鱼中,用[3H]亮氨酸标记的嗅神经蛋白通过慢速轴浆运输,形成一个界限分明的放射性峰。在21℃时,慢速运输以0.92±0.02毫米/天的速度沿轴突移动。已能够分析4种亚细胞组分(可溶性、线粒体和2种膜性组分)及其多肽组成,分析部位包括神经中含有(1)慢速移动峰的区域、(2)峰后神经中残留的物质以及(3)慢速峰前方存在的标记物。在同位素沉积后70天和110天进行了分析。慢速移动放射性峰的特征是,亚细胞组分中的标记与蛋白质浓度之间以及构成这些组分的多肽之间存在紧密的平行关系。放射性主要与分子量为14,000、30 - 45,000、58,000和68,000的分子相关。最后一个峰对应一种未被快速运输标记的蛋白质,仅存在于轻膜性组分中。在所研究的40天期间,移动峰的组成基本保持不变。大多数慢速移动的分子留在移动峰后的轴突中。这种沉积物质似乎比仍在峰中移动的分子重新分布和/或周转得更快。在移动峰前方回收了大量放射性。这可能是由快速运输沉积的分子以及从细胞体以介于快速和慢速运输阶段之间的速率释放的物质产生的。神经该区域的亚细胞和多肽组成保持不变,且介于快速和慢速运输的组成之间。线粒体组分中慢速运输的标记多肽分子量较低,在神经的各个区域以及所研究的两个时间点都发现它们相似,甚至与快速运输所确定的多肽分布相似。