Lammerding-Köppel Maria, Spindler-Barth Margarethe, Drews Ulrich
Institute of Anatomy, University of Tübingen, 72074, Tübingen, Germany.
Institute of Zoology, University of Düsseldorf, 40225, Düsseldorf, Germany.
Rouxs Arch Dev Biol. 1994 Aug;203(7-8):439-444. doi: 10.1007/BF00188693.
The permanent epithelial insect cell line used was derived from Chironomus tentans embryos. Cells are maintained in suspension culture, where they grow as single-layered vesicles. On treatment with the moulting hormone 20-OH-ecdysone cell division ceases. Patches of cuboidal epithelium appear in the vesicles which finally become multilayered and form bud-like protrusions at the outside. In the present study, we localized cholinesterase activity in the cell protrusions by histochemistry and demonstrated coexpression of cholinergic muscarinic receptors by immunofluorescence. Muscarinic receptors were visualized with the monoclonal antibody M35. Six hours after treatment with 20-OH-ecdysone, muscarinic receptors appeared in a few individual cells of the epithelial vesicles before morphological changes became visible. After 24 h, immunofluorescence was concentrated in multilayered patches which now also showed cholinesterase activity. After 3 days, muscarinic receptors and cholinesterase activity were localized in the epithelium protrusions. The results are discussed in the context of an embryonic cholinergic muscarinic system the expression of which has been described in vertebrate and non-vertebrate embryos and is correlated with phases of morphogenesis.
所使用的永久性昆虫上皮细胞系源自摇蚊胚胎。细胞维持悬浮培养,以单层囊泡形式生长。用蜕皮激素20-羟基蜕皮酮处理后,细胞分裂停止。囊泡中出现立方形上皮细胞斑块,最终形成多层结构并在外部形成芽状突起。在本研究中,我们通过组织化学方法定位了细胞突起中的胆碱酯酶活性,并通过免疫荧光证明了胆碱能毒蕈碱受体的共表达。用单克隆抗体M35观察毒蕈碱受体。用20-羟基蜕皮酮处理6小时后,在上皮囊泡的一些单个细胞中出现毒蕈碱受体,此时形态变化尚未可见。24小时后,免疫荧光集中在多层斑块中,此时这些斑块也显示出胆碱酯酶活性。3天后,毒蕈碱受体和胆碱酯酶活性定位于上皮突起中。在胚胎胆碱能毒蕈碱系统的背景下讨论了这些结果,该系统的表达已在脊椎动物和非脊椎动物胚胎中得到描述,并且与形态发生阶段相关。