Sahenk Z, Brown A
Department of Neurology, Ohio State University, College of Medicine, Columbus 43210.
J Neurocytol. 1991 May;20(5):365-75. doi: 10.1007/BF01355533.
Acidotropic weak-base amines were used to investigate the role of acidic compartments in the pathway of aterograde-to-retrograde conversion of axonally transported vesicles in axon terminals. A local concentrated population of nascent axon tips was produced by transecting the rat sciatic nerve in situ to allow local and direct exposure of the axon tips to test solutions. Immersion of the nascent axon tips in solutions containing 10 mM ammonium choloride or 10 mM propylamine caused the axon tips to become distended by an accumulation of elongated membranous tubules and occasional large vacuoles that were both distinct from retrograde organelles. To test whether this accumulation was the result of an impairment of anterograde-to-retrograde conversion, a radioactive pulse-labelling method was used together with a retrograde collection ligature, to quantify the proportion of anterogradely transported proteins that returned from the axon tips by retrograde transport. Exposure of the axon tips to 10 mM ammonium chloride caused the anterogradely transported membrane proteins to accumulate in the axon tips and reduced by about 50% the amount of protein that returned to the retrograde collection ligature. These observations implicate the involvement of acidic membranous compartments in the anterograde-to-retrograde conversion pathway that leads to the formation of retrograde organelles in axon tips. Exposure of nerves to Acridine Orange, which is a vital acidotropic fluorescent dye, confirmed the presence of acidic compartments in the axon tips. Based on these observations, we propose that the membranous tubules that accumulated in the axon tips in the presence of weak-base amines represent a transient intermediate in the pathway of anterograde-to-retrograde conversion of axonally transported vesicles in axon terminals, and that acidic membranous compartments within axon terminals are required for the conversion of these tubules into retrograde organelles.
利用嗜酸性弱碱胺来研究酸性区室在轴突终末轴突运输囊泡顺行到逆行转化途径中的作用。通过原位横断大鼠坐骨神经,产生局部集中的新生轴突尖端群体,以便使轴突尖端局部直接暴露于测试溶液中。将新生轴突尖端浸入含有10 mM氯化铵或10 mM丙胺的溶液中,会导致轴突尖端因细长膜性小管和偶尔出现的大液泡的积累而膨胀,这些都与逆行细胞器不同。为了测试这种积累是否是顺行到逆行转化受损的结果,采用放射性脉冲标记法并结合逆行收集结扎,来量化通过逆行运输从轴突尖端返回的顺行运输蛋白的比例。将轴突尖端暴露于10 mM氯化铵会导致顺行运输的膜蛋白在轴突尖端积累,并使返回逆行收集结扎处的蛋白量减少约50%。这些观察结果表明酸性膜性区室参与了导致轴突尖端形成逆行细胞器的顺行到逆行转化途径。将神经暴露于吖啶橙(一种重要的嗜酸性荧光染料),证实了轴突尖端存在酸性区室。基于这些观察结果,我们提出,在弱碱胺存在下在轴突尖端积累的膜性小管代表轴突终末轴突运输囊泡顺行到逆行转化途径中的一个短暂中间体,并且轴突终末内的酸性膜性区室是将这些小管转化为逆行细胞器所必需的。