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Migratory mechanisms of chick primordial germ cells toward gonadal anlage.

机译:雏鸡原始生殖细胞向性腺迁徙的迁移机制。

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After appearing at the germinal crescent region, chick primordial germ cells (PGCs) migrate toward the presumptive gonads (pG) till stage 19 (Hamburger and Hamilton, 1951). This study seeks to elucidate the roles of passive and active factors in the PGC-migration, physical trapping of circulating PGCs by the capillary network and PGC attraction by chemotactic factor from presumptive gonads. Firstly, latex beads/pollens (the same size or larger than PGCs) were injected into the embryonic bloodstream at stage 13-19 (when PGCs are in the migrating and settlement phase to the presumptive gonad) in ovo in order to determine whether the PGCs passively reach pG. Most of such particles accumulated in the head region (60%), whereas the remainder did the same in the gonadal region (23% at the peak) at stage 16 when both the head and gonadal regions are rich in capillary plexus. After 3 days, most particles in the gonadal region were located at the angles of dorsal mesentery near the developing gonads where many extra-gonadal PGCs had been located, and a few particles were detected close to the gonad. These results suggest that one of the mechanisms of PGC-migration to the developing gonads is an autonomous trapping of PGCs by the capillary network quite close to the germinal epithelium (GE) and passive translocation by morphogenetic movement. Secondly, the attraction for PGCs by the gonadal anlage proper was examined in ovo using chick and quail embryos. Grafts of quail gonadal anlage containing gonadal epithelium and neighbouring mesenchymal tissue were excised from the quail embryo at stages 12 to 16 (staging by Zacchei, 1961). With the aims of eliminating the influence of surrounding tissue, the quail graft was ectopically transplanted into the posterior to the optic vesicle of 8 to 17 somite chick embryo from the point of a posterior region to the auditory vesicle by a fine tungsten needle under the illumination by the method of Hara (1971). Then the region posterior to the level of presumptive vitelline arteries was surgically excised in ovo. After a 48 hrs.-incubation, the host PGCs which lost their own gonadal anlage as a target organ accumulated in the transplanted quail gonadal anlage originating from the embryo at PGC-migrating periods. This result strongly suggested the presence of some attractive factor that may be emitted from the gonadal anlage proper. Furthermore, it was demonstrated that the PGCs in vitro showed no contact inhibition in relation to other PGCs or fibroblasts in their moving pathway.
机译:雏鸡的原始生殖细胞(PGC)出现在新月形的新月形区域后,向假定的性腺(pG)迁移,直到第19阶段(Hamburger和Hamilton,1951年)。这项研究旨在阐明被动和主动因素在PGC迁移,毛细管网络对循环PGC的物理捕获以及假定性腺的趋化因子对PGC的吸引中的作用。首先,将乳胶珠/花粉(大小或大于PGC)在卵内的13-19期(当PGC处于迁移和定居性腺到性腺时)注入胚胎血流中,以确定是否为PGC被动达到pG。当头部和性腺区域都富含毛细血管丛时,大多数此类颗粒在头部区域(60%)中积累,而其余的在性腺区域(在峰值处为23%)表现相同。 3天后,性腺区域中的大多数颗粒位于背侧肠系膜的角度,靠近已发育的性腺PGC所在的发育性腺,并且在性腺附近检测到一些颗粒。这些结果表明,PGC迁移到发育中的性腺的机制之一是通过非常接近生发上皮(GE)的毛细管网络自动捕获PGC,并通过形态发生运动被动转移。其次,使用小鸡和鹌鹑胚胎在卵内检查了性腺正常对PGC的吸引力。在第12到第16阶段从鹌鹑胚胎中切除含有性腺上皮和邻近间充质组织的鹌鹑性腺小体移植物(Zacchei,1961年分期)。为了消除周围组织的影响,在照明条件下,用细钨丝针将鹌鹑移植物从后区到听觉囊的位置异位移植到8至17个m突小鸡胚的视泡后方。通过Hara(1971)的方法。然后在卵内手术切除假定的卵黄动脉水平后的区域。温育48小时后,宿主PGC在PGC迁移期失去作为靶器官的自身性腺异常,其积累在源自胚胎的移植鹌鹑性腺异常中。该结果强烈暗示了可能从性腺正常释放出一些有吸引力的因子。此外,已证明体外PGC在其移动路径中相对于其他PGC或成纤维细胞没有显示出接触抑制作用。

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