Waxman S G, Pappas G D, Bennett M V
J Cell Biol. 1972 Apr;53(1):210-24. doi: 10.1083/jcb.53.1.210.
Electric organs in Sternarchidae are of neural origin, in contrast to electric organs in other fish, which are derived from muscle. The electric organ in Sternarchus is composed of modified axons of spinal neurons. Fibers comprising the electric organ were studied by dissection and by light- and electron microscopy of sectioned material. The spinal electrocytes descend to the electric organ where they run anteriorly for several segments, turn sharply, and run posteriorly to end blindly at approximately the level where they enter the organ. At the level of entry into the organ, and where they turn around, the axons are about 20 micro in diameter; the nodes of Ranvier have a typical appearance with a gap of approximately 1 micro in the myelin. Anteriorly and posteriorly running parts of the fibers dilate to a diameter of approximately 100 micro, and then taper again. In proximal and central regions of anteriorly and posteriorly running parts, nodal gaps measure approximately 1 micro along the axon. In distal regions of anteriorly and posteriorly running parts are three to five large nodes with gaps measuring more than 50 micro along the fiber axis. Nodes with narrow and with wide gaps are distinguishable ultrastructurally; the first type has a typical structure, whereas the second type represents a new nodal morphology. At the typical nodes a dense cytoplasmic material is associated with the axon membrane. At large nodes, the unmyelinated axon membrane is elaborated to form a closely packed layer of irregular polypoid processes without a dense cytoplasmic undercoating. Electrophysiological data indicate that typical nodes in proximal regions of anteriorly and posteriorly running segments actively generate spikes, whereas large distal nodes are inactive and act as a series capacity. Increased membrane surface area provides a morphological correlate for this capacity. This electric organ comprises a unique neural system in which axons have evolved so as to generate external signals, an adaptation involving a functionally significant structural differentiation of nodes of Ranvier along single nerve fibers.
与其他鱼类起源于肌肉的电器官不同,电鳗科的电器官起源于神经。电鳗的电器官由脊髓神经元的修饰轴突组成。通过解剖以及对切片材料进行光学显微镜和电子显微镜观察,研究了构成电器官的纤维。脊髓电细胞向下延伸至电器官,在那里它们向前延伸几个节段,急剧转弯,然后向后延伸,在进入器官的大致水平处盲端终止。在进入器官的水平以及转弯处,轴突直径约为20微米;郎飞结外观典型,髓鞘间隙约为1微米。纤维向前和向后延伸的部分扩张至直径约为100微米,然后再次变细。在向前和向后延伸部分的近端和中央区域,沿轴突的节点间隙约为1微米。在向前和向后延伸部分的远端区域,有三到五个大节点,沿纤维轴的间隙超过50微米。间隙窄和间隙宽的节点在超微结构上是可区分的;第一种类型具有典型结构,而第二种类型代表一种新的节点形态。在典型节点处,致密的细胞质物质与轴突膜相关。在大节点处,无髓鞘的轴突膜形成一层紧密堆积的不规则息肉状突起,没有致密的细胞质底层。电生理数据表明,向前和向后延伸节段近端区域的典型节点可主动产生动作电位,而远端大节点不活跃,起到串联电容的作用。膜表面积的增加为这种电容提供了形态学上的关联。这种电器官包含一个独特的神经系统,其中轴突已经进化到能够产生外部信号,这种适应涉及沿单根神经纤维的郎飞结在功能上具有重要意义的结构分化。