Department of Invertebrate Zoology, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia.
Laboratory of Ocean Benthic Fauna, Shirshov Institute of Oceanology of the Russian Academy of Science, Moscow, Russia.
PLoS One. 2018 Dec 13;13(12):e0198271. doi: 10.1371/journal.pone.0198271. eCollection 2018.
Tracing the evolution of the siboglinid group, peculiar group of marine gutless annelids, requires the detailed study of the fragmentarily explored central nervous system of vestimentiferans and other siboglinids. 3D reconstructions of the neuroanatomy of Riftia revealed that the "brain" of adult vestimentiferans is a fusion product of the supraesophageal and subesophageal ganglia. The supraesophageal ganglion-like area contains the following neural structures that are homologous to the annelid elements: the peripheral perikarya of the brain lobes, two main transverse commissures, mushroom-like structures, commissural cell cluster, and the circumesophageal connectives with two roots which give rise to the palp neurites. Three pairs of giant perikarya are located in the supraesophageal ganglion, giving rise to the paired giant axons. The circumesophageal connectives run to the VNC. The subesophageal ganglion-like area contains a tripartite ventral aggregation of perikarya (= the postoral ganglion of the VNC) interconnected by the subenteral commissure. The paired VNC is intraepidermal, not ganglionated over most of its length, associated with the ciliary field, and comprises the giant axons. The pairs of VNC and the giant axons fuse posteriorly. Within siboglinids, the vestimentiferans are distinguished by a large and considerably differentiated brain. This reflects the derived development of the tentacle crown. The tentacles of vestimentiferans are homologous to the annelid palps based on their innervation from the dorsal and ventral roots of the circumesophageal connectives. Neuroanatomy of the vestimentiferan brains is close to the brains of Cirratuliiformia and Spionida/Sabellida, which have several transverse commissures, specific position of the giant somata (if any), and palp nerve roots (if any). The palps and palp neurite roots originally developed in all main annelid clades (basally branching, errantian and sedentarian annelids), show the greatest diversity in their number in sedentarian species. Over the course of evolution of Sedentaria, the number of palps and their nerve roots either dramatically increased (as in vestimentiferan siboglinids) or were lost.
研究特殊的海洋无肠环节动物 siboglinid 群的进化,需要详细研究 Vestimentiferans 和其他 siboglinid 中探索不足的中央神经系统。Riftia 的神经解剖结构重建表明,成年 Vestimentiferans 的“大脑”是上食管神经节和下食管神经节的融合产物。上食管神经节状区域包含以下与环节动物同源的神经结构:脑叶的外周神经原、两个主要的横神经索、蕈状结构、神经索细胞群以及具有两个根的环绕食管连接体,这些根产生触须神经纤维。三个巨大的神经原位于上食管神经节,产生成对的巨大轴突。环绕食管连接体延伸到 VNC。上食管神经节状区域包含一个由三个部分组成的腹侧聚集的神经原(= VNC 的后口腔神经节),由下内脏神经索连接。成对的 VNC 是表皮内的,在其大部分长度上没有神经节,与纤毛场相关联,并包含巨大的轴突。成对的 VNC 和巨大的轴突在后部融合。在 siboglinids 中, Vestimentiferans 以其较大且分化程度较高的大脑为特征。这反映了触须冠的衍生发育。 Vestimentiferans 的触须基于其从环绕食管连接体的背根和腹根的神经支配,与环节动物的触须同源。Vestimentiferan 大脑的神经解剖结构与 Cirratuliiformia 和 Spionida/Sabellida 的大脑相似,它们具有多个横神经索、特定的巨大体位置(如果有的话)和触须神经根(如果有的话)。触须和触须神经根最初在所有主要环节动物类群中发育(基底分支、游离和固着环节动物),在固着物种中其数量表现出最大的多样性。在 Sedentaria 的进化过程中,触须和它们的神经根的数量要么急剧增加(如 Vestimentiferan siboglinids 中那样),要么丢失。