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日本海羊齿(棘皮动物门:海百合纲)原肠胚阶段胚胎的精细结构。

The fine structure of the embryo during the gastrula stage of Comanthus japonica (Echinodermata: Crinoidea).

作者信息

Holland N D

出版信息

Tissue Cell. 1976;8(3):491-510. doi: 10.1016/0040-8166(76)90009-4.

DOI:10.1016/0040-8166(76)90009-4
PMID:982423
Abstract

The fine structure of the embryo of Comanthus has been described by scanning and transmission electron microscopy at two-hourly intervals throughout the gastrula stage (from the fifth through the fifteenth hours of development). At 5 hr, gastrulation has occurred in the absence of any structure comparable to the echinoid hyaline layer; therefore, at least one important mechanism proposed for echinoid gastrulation cannot occur in this crinoid. At 7 hr, the blastocoelic basal lamina has formed, and all ectodermal and entodermal nuclei contain dense aggregates, which are probably perichromatin fibrils. At 9 hr, the blastocoel contains mesenchyme cells, presumably of entodermal origin. At 11 hr, ciliogenesis has started at the apical surfaces of the ectoderm cells and at the archenteral surfaces of the entoderm cells; many of the newly formed cilia are swollen subterminally. At 13 hr, a conspicuous glycocalyx is beginning to cover the apical ends of the ectoderm cells, and the fertilization membrane is beginning to dissolve from its inner surface. Between 5 and 13 hr, there is a gradual development of a junctional complex associating the apicolateral margins of the ectoderm cells; the zonula adherens part of the complex appears at 5 hr and is well developed by 7 hr, and then the septate junction part of the complex appears at 9 hr and is well developed by 13 hr. At 15 hr, the blastopore has closed, the ectodermal glycocalyx is fully developed, some mesenchyme cells appear to be differentiating into skeleton forming cells, and the fertilization membrane is in the last stages of dissolution.

摘要

通过扫描电子显微镜和透射电子显微镜,每隔两小时对海百合胚胎原肠胚阶段(从发育的第5小时到第15小时)的精细结构进行了描述。在5小时时,原肠胚形成,没有任何与海胆类透明层类似的结构;因此,至少一种为海胆类原肠胚形成提出的重要机制在这种海百合中无法发生。在7小时时,囊胚腔基膜形成,所有外胚层和内胚层细胞核都含有致密聚集体,可能是染色质外周纤维。在9小时时,囊胚腔含有间充质细胞,推测起源于内胚层。在11小时时,外胚层细胞顶端表面和内胚层细胞原肠表面开始发生纤毛形成;许多新形成的纤毛在末端附近肿胀。在13小时时,明显的糖萼开始覆盖外胚层细胞的顶端,受精膜开始从其内表面溶解。在5小时到13小时之间,外胚层细胞顶端外侧边缘逐渐形成连接复合体;复合体的黏着小带部分在5小时出现并在7小时发育良好,然后复合体的分隔连接部分在9小时出现并在13小时发育良好。在15小时时,胚孔关闭,外胚层糖萼完全发育,一些间充质细胞似乎正在分化为形成骨骼的细胞,受精膜处于溶解的最后阶段。

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