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青蛙运动神经元快速轴突运输所需的钙

Calcium requirement for fast axonal transport in frog motoneurons.

作者信息

Larivière L, Lavoie P A

出版信息

J Neurochem. 1982 Sep;39(3):882-6. doi: 10.1111/j.1471-4159.1982.tb07976.x.

Abstract

Calcium is required to sustain fast axonal transport in sensory neurons of frog and cat. We studied the Ca2+ dependence of fast axonal transport in the motoneurons of the lower spinal cord from frog. The accumulation of acetylcholinesterase at a crush on the ventral roots was used to follow axonal transport. Two types of experiments were performed: modification of the medium bathing the ventral roots, alone, and modification of the medium bathing the spinal cord and ventral roots. Incubation (17--18 h) of the ventral roots in Ca2+-free medium markedly inhibited acetylcholinesterase transport, a finding that demonstrates a Ca2+ requirement for fast axonal transport in motoneurons; when 4 mM MgCl2 was added to the Ca2+-free medium, transport was also greatly reduced. During incubation of the ventral roots in normal medium supplemented with 0.18 mM CoCl2 transport proceeded normally; but when the Co2+ concentration was raised to 1.8 mM, transport was diminished as drastically as in the Ca2+-free medium. Incubation of the spinal cord and ventral roots in medium containing 0.18 mM CoCl2 did not reduce the accumulation of acetylcholinesterase at the crush. Similarly, accumulation of acetylcholinesterase at a crush on the dorsal root was not significantly reduced by exposure of the dorsal root ganglion and root to 0.18 mM Co2+. Exposure of sensory cell bodies to 0.18 mM Co2+ thus produces differential effects on transport of acetylcholinesterase and on transport of newly synthesized radiolabeled protein.

摘要

维持青蛙和猫的感觉神经元中的快速轴突运输需要钙。我们研究了青蛙下脊髓运动神经元中快速轴突运输对Ca2+的依赖性。利用腹根挤压处乙酰胆碱酯酶的积累来追踪轴突运输。进行了两类实验:单独改变浸泡腹根的培养基,以及改变浸泡脊髓和腹根的培养基。将腹根在无Ca2+的培养基中孵育(17 - 18小时)显著抑制了乙酰胆碱酯酶的运输,这一发现表明运动神经元中的快速轴突运输需要Ca2+;当向无Ca2+的培养基中添加4 mM MgCl2时,运输也大大减少。在补充了0.18 mM CoCl2的正常培养基中孵育腹根时,运输正常进行;但当Co2+浓度提高到1.8 mM时,运输减少的程度与在无Ca2+的培养基中一样剧烈。将脊髓和腹根在含有0.18 mM CoCl2的培养基中孵育并没有减少挤压处乙酰胆碱酯酶的积累。同样,将背根神经节和背根暴露于0.18 mM Co2+并不会显著降低背根挤压处乙酰胆碱酯酶的积累。因此,将感觉细胞体暴露于0.18 mM Co2+会对乙酰胆碱酯酶的运输和新合成的放射性标记蛋白的运输产生不同的影响。

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