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Trophoblast glycogen cells differentiate early in the mouse ectoplacental cone: putative role during placentation.

机译:滋养层糖原细胞在小鼠外胎盘锥中早期分化:在胎盘形成过程中的假定作用。

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The role of differentiated trophoblast glycogen cells (GCs) in the ectoplacental cone (EPC) has not been elucidated yet. Recently, GC progenitors have been shown to be present from embryonic day 7.5 (E7.5), but glycogen is found in GC only from E10.5. Herein, we investigated the origin, localization and characterization of mouse GCs in EPC and their relationship with blood cells and trophoblast giant cells (TGCs) during placentation. Implantation sites (E5.5-E12.5) were processed for histological studies, histochemical detection (glycogen) and immunohistochemical staining (Ki67). Three-dimensional reconstruction of the EPC was obtained from suitably oriented embryos at E7.5. Our findings evidence that GCs are present and assembled in clusters from E6.5 to E12.5, and that they exhibit the classic vacuolated appearance and contain PAS-positive glycogen, which is amylase-sensitive and acetylation-resistant. In fact, only GCs were stained after acetylation, confirming unequivocally their presence in tissues. At E6.5, GCs showed numerous mitoses and vacuoles with scattered glycogen particles. At E7.5, GCs showed low numbers of mitoses and abundant vacuoles full of glycogen. During E7.5-E8.5, GCs were in close proximity to TGCs, and cells were intercalated by thin maternal blood spaces; placental GCs lost maternal blood contact during E9.5-E12.5. Our results indicate that GCs are originated and proliferate in the upper portion in the midregion of EPC at E6.5, and that at E7.5-E8.5 they show consistent glycogen deposits, which are likely metabolized to glucose. This compound may be directly transferred to circulating maternal blood, and used as a source of energy by GCs and TGCs during placentation.
机译:尚未阐明分化的滋养层糖原细胞(GCs)在外胎盘锥体(EPC)中的作用。最近,已证明从胚胎第7.5天(E7.5)起就存在GC祖细胞,但仅从E10.5起才在GC中发现糖原。在这里,我们调查了小鼠GC在EPC中的起源,定位和特性,以及它们在胎盘形成过程中与血细胞和滋养层巨细胞(TGC)的关系。植入部位(E5.5-E12.5)进行了组织学研究,组织化学检测(糖原)和免疫组织化学染色(Ki67)。 EPC的三维重建是从E7.5处适当定向的胚胎获得的。我们的发现证明,GC从E6.5到E12.5呈簇状存在和组装,它们表现出经典的空泡外观,并含有淀粉酶敏感和抗乙酰化的PAS阳性糖原。实际上,乙酰化后只有GC被染色,从而明确证实了它们在组织中的存在。在E6.5时,GC显示许多有丝分裂和液泡,并带有分散的糖原颗粒。在E7.5时,GC显示出较少的有丝分裂和充满糖原的丰富液泡。在E7.5-E8.5期间,GC靠近TGC,并且细胞被薄薄的母体血液间隙插入;胎盘GC在E9.5-E12.5期间失去母体血液接触。我们的结果表明,GC在E6.5的EPC中部区域的上部起源并扩散,在E7.5-E8.5时它们显示出一致的糖原沉积,可能被代谢为葡萄糖。该化合物可直接转移到循环的母体血液中,并在胎盘形成过程中被GC和TGC用作能量来源。

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