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首页> 外文期刊>Journal of Reproductive Immunology >Is the zona pellucida an intrinsic source of signals activating maternal recognition of the developing mammalian embryo?
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Is the zona pellucida an intrinsic source of signals activating maternal recognition of the developing mammalian embryo?

机译:透明带是激活母体对发育中的哺乳动物胚胎的母体识别的信号的内在来源吗?

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Mammalian mothers undergoing embryo implantation must specifically recognize the developing embryo in a species-restricted manner. We previously observed that immune cells derived from early pregnant mice could promote endometrial differentiation and embryo implantation in blastocyst-transferred pseudopregnant mice. Although the precise mechanism remains unknown, it is suggested that the maternal immune system undergoes functional changes after recognizing developing embryos from the very early stages of pregnancy. Since it is physically impossible for immune cells to directly interact with the developing embryo while it is surrounded by the zona pellucida (ZP), it is speculated that the embryo produces certain embryo- and species-specific soluble factor(s) in the oviduct before hatching. As a candidate for this factor, we have paid attention to the ZP that is normally protected from immunological attack during oogenesis in the ovarian follicle. ZP-specific glycoproteins are known to play important roles in the species- and oocyte-specific binding of sperm, and the ZP can also be considered an abundant store of oocyte- and species-specific glycoproteins. In contrast to unfertilized oocytes, developing embryos may degrade the ZP starting just after fertilization and proceeding until hatching using enzymes that are released from cortical granules or produced by the developing embryo. Accordingly, the developing embryo might provide ZP-degradation products including oligosaccharide chains to the immune system from the very early stages. Taken together, we propose here a novel hypothesis that these ZP-derivatives can act as an intrinsic signal from the developing embryo for maternal recognition by the immune system.
机译:接受胚胎植入的哺乳动物母亲必须以物种限制的方式特异性识别发育中的胚胎。我们以前观察到,早孕小鼠衍生的免疫细胞可以促进胚泡转移假孕小鼠的子宫内膜分化和胚胎植入。尽管确切的机制尚不清楚,但建议母体免疫系统在识别出从妊娠早期开始发育的胚胎后就会发生功能变化。由于在透明带(ZP)包围下免疫细胞在物理上不可能与发育中的胚胎直接相互作用,因此推测该胚胎会在输卵管中产生某些特定于胚胎和物种的可溶性因子。孵化。作为该因素的候选者,我们已经关注了ZP,该蛋白通常在卵泡卵子发生过程中受到免疫攻击的保护。已知ZP特异性糖蛋白在精子的物种和卵母细胞特异性结合中起重要作用,并且ZP也可以被认为是卵母细胞和物种特异性糖蛋白的丰富储备。与未受精的卵母细胞相反,发育中的胚胎可能会在受精后立即降解ZP,然后继续进行直到使用从皮质颗粒释放的酶或发育中的胚胎产生的酶孵化为止。因此,正在发育的胚胎可能从很早的阶段就向免疫系统提供包括寡糖链的ZP降解产物。综上所述,我们在这里提出一个新颖的假设,即这些ZP衍生物可以作为来自发育中胚胎的内在信号,以被免疫系统识别为母体。

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