Yamada K M, Spooner B S, Wessells N K
J Cell Biol. 1971 Jun;49(3):614-35. doi: 10.1083/jcb.49.3.614.
Dorsal root ganglion nerve cells undergoing axon elongation in vitro have been analyzed ultrastructurally. The growth cone at the axonal tip contains smooth endoplasmic reticulum, vesicles, neurofilaments, occasional microtubules, and a network of 50-A in diameter microfilaments. The filamentous network fills the periphery of the growth cone and is the only structure found in microspikes. Elements of the network are oriented parallel to the axis of microspikes, but exhibit little orientation in the growth cone. Cytochalasin B causes rounding up of growth cones, retraction of microspikes, and cessation of axon elongation. The latter biological effect correlates with an ultrastructural alteration in the filamentous network of growth cones and microspikes. No other organelle appears to be affected by the drug. Removal of cytochalasin allows reinitiation of growth cone-microspike activity, and elongation begins anew. Such recovery will occur in the presence of the protein synthesis inhibitor cycloheximide, and in the absence of exogenous nerve growth factor. The neurofilaments and microtubules of axons are regularly spaced. Fine filaments indistinguishable from those in the growth cone interconnect neurofilaments, vesicles, microtubules, and plasma membrane. This filamentous network could provide the structural basis for the initiation of lateral microspikes and perhaps of collateral axons, besides playing a role in axonal transport.
已对体外轴突伸长的背根神经节神经细胞进行了超微结构分析。轴突末端的生长锥含有滑面内质网、囊泡、神经丝、偶尔的微管以及直径为50埃的微丝网络。丝状网络充满生长锥的周边,是微棘中唯一发现的结构。网络元件与微棘轴平行排列,但在生长锥中几乎没有方向性。细胞松弛素B导致生长锥变圆、微棘回缩以及轴突伸长停止。后一种生物学效应与生长锥和微棘丝状网络的超微结构改变相关。似乎没有其他细胞器受该药物影响。去除细胞松弛素可使生长锥 - 微棘活性重新启动,伸长重新开始。这种恢复将在存在蛋白质合成抑制剂环己酰亚胺且不存在外源性神经生长因子的情况下发生。轴突的神经丝和微管有规则地间隔排列。与生长锥中的细丝无法区分的细丝将神经丝、囊泡、微管和质膜相互连接。这种丝状网络除了在轴突运输中起作用外,还可为侧向微棘以及可能的侧支轴突的起始提供结构基础。