Hartenstein V, Tepass U, Gruszynski-Defeo E
Department of Biology, University of California at Los Angeles 90024.
J Comp Neurol. 1994 Dec 15;350(3):367-81. doi: 10.1002/cne.903500304.
Using several cell-specific markers, the pattern of proliferation, morphogenesis, and neuronal differentiation of the Drosophila larval stomatogastric nervous system (SNS) was analyzed. In the late embryo, four SNS ganglia (frontal ganglion, hypocerebral ganglion, paraesophageal ganglion, ventricular ganglion) can be distinguished. In the early embryo, the precursor cells of the SNS (SNSPs), being an integral part of the anlage of the esophagus, undergo four synchronous rounds of division. Subsequently, SNSPs segregate from the esophageal epithelium in a complex and stereotyped pattern. The majority of SNSPs invaginate and transiently form three (rostral, intermediate, caudal) pouches that, after separating from the esophagus, become epithelial vesicles. At later stages, these SNSPs gradually lose their epithelial phenotype. Starting at the anterior-dorsal tip of each vesicle, SNSPs dissociate from one another and migrate to the various locations where they differentiate as neurons. Cells of the rostral and intermediate vesicle contribute to the frontal ganglion; the hypocerebral ganglion develops from the intermediate vesicle, the paraesophageal ganglion from the rostral vesicle, and the ventricular ganglion from the caudal vesicle. In addition to the invaginating SNSPs, several distinct groups of SNSPs delaminate as individual cells from the esophageal epithelium. Three clusters of SNSPs delaminate from a region anterior to the rostral pouch; a single SNSP delaminates from the tip of each pouch. All delaminating SNSPs contribute to the frontal ganglion. A significant number of SNSPs undergo cell death. In the late embryo, the stomatogastric ganglia are interconnected by the recurrent nerve and esophageal nerves. The frontal ganglion projects to the brain via the frontal connectives. Both recurrent nerve and frontal connectives are pioneered by small subpopulations of early differentiating stomatogastric neurons that most likely derive from among the dSNSPs and iSNSPs.
利用多种细胞特异性标记物,对果蝇幼虫口胃神经系统(SNS)的增殖、形态发生和神经元分化模式进行了分析。在胚胎后期,可以区分出四个SNS神经节(额神经节、脑下神经节、食管旁神经节、心室神经节)。在胚胎早期,SNS的前体细胞(SNSPs)作为食管原基的一个组成部分,经历四轮同步分裂。随后,SNSPs以复杂且固定的模式从食管上皮中分离出来。大多数SNSPs内陷并短暂形成三个(头端、中间、尾端)囊袋,这些囊袋从食管分离后成为上皮小泡。在后期阶段,这些SNSPs逐渐失去其上皮表型。从每个小泡的前背端开始,SNSPs彼此分离并迁移到它们分化为神经元的不同位置。头端和中间小泡的细胞形成额神经节;脑下神经节由中间小泡发育而来,食管旁神经节由头端小泡发育而来,心室神经节由尾端小泡发育而来。除了内陷的SNSPs,还有几群不同的SNSPs作为单个细胞从食管上皮层脱离。三群SNSPs从位于头端囊袋前方的一个区域脱离;每个囊袋的顶端有一个SNSPs脱离。所有脱离的SNSPs都对头端神经节有贡献。大量的SNSPs会发生细胞死亡。在胚胎后期,口胃神经节通过返神经和食管神经相互连接。额神经节通过额神经连合投射到脑。返神经和额神经连合都是由早期分化的口胃神经元的小亚群先驱形成的,这些神经元很可能来自dSNSPs和iSNSPs。