Dailey M E, Bridgman P C
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, MO 63110.
J Neurosci Res. 1991 Sep;30(1):242-58. doi: 10.1002/jnr.490300125.
Advance and stabilization of organelle-rich cytoplasm within the neuronal growth cone is coupled to axon elongation (Goldberg and Burmeister, 1986; Aletta and Greene, 1988), and this involves forward movement of organelles from the growth cone base along distinct tracks toward the leading edge. Membrane-bound organelles that advance first within the growth cone often make transient excursions toward the leading edge, and at the light microscope level these leading organelles appear to colocalize with distal microtubule (MT) segments (Dailey and Bridgman, 1989). We have used electron microscopy (EM) to identify the membranous organelles adjacent to distal MT segments, and to examine their structural interactions with MTs. In both glutaraldehyde-fixed and rapid frozen whole-mount growth cones, attenuated endoplasmic reticulum (ER)-like membrane elements were the most common organelle type located adjacent to distal MT segments. These ER-like membrane elements coursed roughly parallel to MTs and frequently terminated within an electron-dense bulb at the MT tip. Blind-ended membrane tubes, dense-core vesicles, clear vesicles, and vacuoles were also found adjacent to distal MT segments. Quantitative analyses of organelle-MT associations suggest that elements of the ER-like membrane system may frequently advance ahead of other membrane-bound organelles. Freeze-etch EM revealed crossbridging structures between MTs and membranous organelles, which is consistent with the idea that advance of leading membrane organelles into the growth cone periphery is mediated by microtubule-based motor transport mechanisms. The results suggest that distal microtubule segments serve as transport elements for advance of membrane organelles into more peripheral growth cone regions, and together MTs and ER-like membrane organelles may initiate the conversion of dynamic F-actin-rich cytoplasm to more stable organelle-rich cytoplasm (i.e., axoplasm).
神经元生长锥内富含细胞器的细胞质的推进和稳定与轴突伸长相关联(戈德堡和伯迈斯特,1986年;阿莱塔和格林,1988年),这涉及细胞器从生长锥基部沿着不同轨道向前移动至前沿。在生长锥内首先推进的膜结合细胞器常常会短暂地向前沿偏移,并且在光学显微镜水平下,这些前沿细胞器似乎与远端微管(MT)节段共定位(戴利和布里奇曼,1989年)。我们利用电子显微镜(EM)来识别与远端MT节段相邻的膜性细胞器,并研究它们与微管的结构相互作用。在戊二醛固定和快速冷冻的整装生长锥中,类似内质网(ER)的衰减膜元件是位于远端MT节段附近最常见的细胞器类型。这些类似ER的膜元件大致与微管平行延伸,并常常在微管尖端的电子致密球体内终止。盲端膜管、致密核心囊泡、清亮囊泡和液泡也在远端MT节段附近被发现。对细胞器 - 微管关联的定量分析表明,类似ER的膜系统元件可能经常比其他膜结合细胞器提前推进。冷冻蚀刻电子显微镜揭示了微管与膜性细胞器之间的交叉桥结构,这与前沿膜细胞器向生长锥周边推进是由基于微管的马达运输机制介导的观点一致。结果表明,远端微管节段作为膜细胞器向更外围生长锥区域推进的运输元件,并且微管和类似ER的膜细胞器共同可能启动富含动态F - 肌动蛋白的细胞质向更稳定的富含细胞器的细胞质(即轴质)的转变。