禽胚的卵母细胞组成层和原始生殖细胞蛋黄的起源。

M Callebaut
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引用次数: 0

摘要

通过放射性或台诱蓝诱导的荧光蛋黄标记(在某些发育阶段用作活体细胞质标记),可以证明,当前体卵母细胞从3 mm生长到大约18 mm(快速生长期)时,形成了鹌鹑囊胚的组成蛋黄层。先前的一项研究(Callebaut, 1974)和目前的研究表明,在禽类生发盘中可以识别出两个细胞质区域,每个区域具有不同的结构和行为:1)在卵子发生过程中,含有与t.i.c.o.s (3h -胸腺嘧啶结合细胞器)接触的蛋黄;2)表面和外围区域,该区域未与T.I.C.O.材料接触,并随着解理沟渗透到第一区域。在大卵裂球中,原来浅层的卵浆包围着深层的卵浆。未孵育胚皮的中央区域必须被认为是一个异质细胞群,含有不同数量的深层和表层物质。产蛋孵化后,卵黄内胚层和生长过度边缘等胚外组织在浅部和外周发育。胚胎中胚层也由后者发育而来。将被纳入原始生殖细胞(生发卵黄)的卵黄仅来自卵母细胞生发盘的原始深层和近轴区域,即来自与t.c.o.s接触的区域。生发卵黄质可在卵母细胞生发盘的深层近轴区域、未孵化胚皮的中心区域找到。在内膜(早期原始条纹期),最后在原始生殖细胞(P.G.C.s)与内膜壁分离时(早期体期)。因此,我们的结果为禽类灯刷后卵母细胞中存在生殖细胞质提供了证据。
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The constituent oocytal layers of the avian germ and the origin of the primordial germ cell yolk.

By radioactive or trypan blue induced fluorescence yolk labelling (used at certain developmental stages as intravital cytoplasmic markers), it can be demonstrated that the constituent yolk layers of quail blastoderms are formed when the precursor oocyte is growing from 3 to approximately 18 mm (rapid growth period). A previous study ( Callebaut , 1974) and the present study demonstrate that 2 cytoplasmic regions, each with a different constitution and behaviour, can be discerned in the avian germinal disc: 1) a deep and paraxial region, containing yolk that has been in contact with the t.i.c.o.s. (3H-thymidine incorporating cytoplasmic organelles) during oogenesis; 2) a superficial and peripheral region, which has not been in contact with the t.i.c.o. material and which penetrates into the first region along with the cleavage furrows. In the large blastomeres, the originally superficial ooplasm surrounds the deep ooplasm. The area centralis of the unincubated blastoderm must be considered as a heterogeneous cell population, containing both deep and superficial material in variable amounts. After laying and incubation, extra-embryonic tissues such as yolk endoderm and margin of overgrowth develop in the superficial and peripheral region. The embryonic mesoderm also develops from the latter. The yolk, which will be incorporated in the primordial germ cells (germinal yolk), derives only from the original deep and paraxial region of the oocytal germinal disc, i.e. from the region which has been in contact with the t.i.c.o.s. The germinal yolk plasm can be traced in the deep paraxial region of the oocytal germinal disc, in the central region of the unincubated blastoderm, in the endophyll (early primitive streak stage) and finally in the primordial germ cells (P.G.C.s.) at the moment of their separation from the endophyll wall (early somite stage). Thus our results provide evidence for the existence of a germ cell plasm in the avian postlampbrush oocyte.

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