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过去记述的嵌合体,都是将卵裂期的胚细胞聚合在一起,或者将细胞注入胚泡的胚泡腔以后,返回到假妊养母的子宫里。因为着床前的胚胎,是悬浮在输卵管或子官腔内,能够取出在试管内进行各种操作。而着床以后,胚胎在 相似文献
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胚泡着床窗口的分子调控 总被引:5,自引:0,他引:5
着床窗口是指当胚胎发育到胚泡阶段时,子宫也增殖和分化到可接受状态,二者相互作用使胚泡着床的短暂时间.雌激素和孕酮是该过程的综合调控分子,它们通过多种局部信号分子的介导,使子宫中的各种细胞类型增殖、分化,为着床窗口的开放做出相互协调的反应.子宫与胚胎在着床窗口通过前列腺素、组织胺、降钙素、多种细胞因子和生长因子的旁分泌作用进行分子对话,使胚泡滋养层与子宫内膜上皮发生附着反应.着床窗口一旦开放,即自动向非接受态转化. 相似文献
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胚胎着床是处于活化状态的胚泡与处于接受态的子宫相互作用,最后导致胚胎滋养层与子宫内膜建立紧密联系的过程。已证实白血病抑制因子(LIF)在哺乳动物胚胎着床过程中起着十分重要的调节作用。LIF通过其受体及信号传递亚单位gp130发挥其生物学功能。LIF对胚胎发育到胚泡阶段及以后内细胞团和滋养层细胞的生长和分化有明显的促进作用。 在小鼠中,LIF及其受体和gp130在着床期小鼠子宫内表达量最高,因此LIF可能在小鼠胚胎着床过程中起重要作用。在人中,LIF在子宫内膜中的表达与人胚胎着床的时间一致,提示LIF可能与人的胚胎着床紧密相关。此外,LIF在猪、羊、水貂、兔和臭鼬等动物胚泡着床前和着床期的子宫中也都有表达,并在着床期出现峰值。因此,LIF也可能在这些动物的胚胎发育和着床过程中有重要作用。LIF受体基因敲除小鼠表现为胎盘发育不全,这说明LIF对小鼠胎盘形成和胎盘的功能维持起重要作用。 小鼠子宫中LIF的表达可能受雌激素而上调。美洲长尾猴(绒)及兔子宫中LIF的表达则呈孕酮依赖性。然而孕酮可抑制人着床期子宫内膜腺上皮和蜕膜组织内LIF的表达。在不同种类的动物中,LIF在子宫中的表达有不同的调节机制。 胚泡在LIF基因敲除的雌鼠子宫内不能着床的原因并不是由于胚泡发育异常,而是由于雌鼠不能表 相似文献
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哺乳动物胚泡着床是生殖过程中的关键环节。受精卵经过早期发育形成了胚泡,胚泡脱去透明带后,经定位、粘附、滋养层侵入,植入到子宫内膜中,同时母体子宫内膜发生蜕膜化控制植入的程度,最终完成着床过程。着床过程受多种因素的影响,主要因素有:母体子宫内膜和胚泡发育的同步化,母体的激素环境,胚泡分泌的激素,母体子宫的接受性及局部免疫保护作用。 相似文献
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生命过程的相似性--从着床部位母体细胞的凋亡谈起 总被引:2,自引:0,他引:2
胚胎着床受许多因素的精确调控,其中着床部位母体细胞的凋亡在围植入期执行着重要的生理任务。但它自身的发生机制尚不完全清楚,在胚胎着床中的调节机制就更远远落后于凋亡在其他系统领域中的相知程度。因此,对细胞凋亡在着床部位母体细胞中出现的深入研究,将进一步完善我们对着床机制的理解,同时,因为肿瘤和胚胎对机体作用相似性也使这个领域的研究具有特殊的意义。 相似文献
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目的 研究肿瘤转移抑制因子CD63/ME491 mRNA和蛋白在植入前小鼠胚胎及延迟着床小鼠子宫中的表达规律,探讨其在胚胎着床过程中的作用以及雌激素对其表达的调节.方法 应用RT-PCR、免疫荧光、免疫组化技术观察CD63/ME491 mRNA和蛋白的表达规律.结果 在植入前小鼠胚胎中均有CD63/ME491 mRNA及其蛋白表达.CD63/ME491 mRNA在桑葚胚及囊胚期表达较丰富,CD63/ME491蛋白表达于各期胚胎细胞的胞膜和胞浆;CD63/ME491 mRNA在延迟着床小鼠子宫均有表达,但从D5到D8呈下降趋势,雌二醇(E2)激活后mRNA的表达显著上升(P<0.05).CD63/ME491蛋白在延迟着床D5弱表达于上皮下基质细胞,D6~8表达不明显,E2激活后该蛋白明显表达于上皮下基质细胞的胞膜和胞浆.结论 1. CD63/ME491在植入前小鼠胚胎中呈动态表达,提示它参与了胚胎的发育过程;2. CD63/ME491在小鼠子宫中的表达可能受雌激素调节. 相似文献
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胚胎着床是一个连续的动态过程,其中胚泡从透明带中准时孵出是着床的关键.透明带脱落的机制主要是子宫或(和)胚泡分泌物部分或全部溶解透明带后,胚泡在细胞数量增加及细胞运动的机械压力作用下通过透明带的某一位点孵出. 相似文献
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前列腺素F(PGF)抗血清对小鼠胚泡着床的影响 总被引:1,自引:1,他引:1
本文试图利用自制的PGP抗血清,对小鼠子宫局部进行注射,以观察其对胚泡着床的影响。结果表明,于妊娠第3天(孕卵在输卵管阶段)单侧子宫角注射PGF抗血清,对胚泡着床无影响。而妊娠第4天(胚泡在子宫阶段〕单侧或双侧子宫角注射PGF抗血清,对胚泡着床均有明显的抑制作用。这一结果提示小鼠胚泡着床中PGF起着重要的作用。 相似文献
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蛋白酶抑制剂对小鼠胚泡着床的作用 总被引:2,自引:0,他引:2
本文采用子宫内注射和胚胎与子宫上皮细胞在体外共培养的方法,研究几种蛋白酶抑制对小鼠胚胎着床的影响。实验结果显示,蛋白酶抑制剂STI,EACA和NPGB均能显著抑制胚泡在子宫内着床;STI和EACA能有效地抑制胚泡在子宫上皮细胞单层上的扩展,而NPGB对胚泡在子宫上皮细胞单层上的粘附和扩展均有显著的抑制作用。 相似文献
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PPARs信号通路与哺乳动物生殖 总被引:1,自引:0,他引:1
过氧化物酶体增殖因子活化受体(peroxisome proliferator-activated receptors,PPARs)在动物体内有着广泛的生物学作用,可调节脂类代谢、能量收支平衡以及细胞分裂分化等重要生理过程。已经发现,PPARs信号通路与糖尿病和癌症等许多重大疾病的发生有关。随着基因剔除技术的应用以及PPARs人工配体的开发利用,人们对PPARs的认识不断深入。现对PPARs通路在卵巢周期、黄体形成、胚胎着床、胎盘发育和雄性生殖等哺乳动物生殖系统中的表达、功能及作用机制进行综述。 相似文献
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Einarsson EJ 《Theriogenology》1985,24(4):375-383
In 1980 and 1981, respectively, 12 and 19 one-year-old mink females of standard and jetblack breeds were used to determine the progesterone level approximately at the time of expected implantation. Blood samples were collected every 2 to 3 days or daily in order to accurately estimate the time of increase in plasma progesterone levels. The results indicate that the progesterone level increased to above 10 ng/ml, 31.6 (sigma = 1.3) days prior to parturition on the average. This was supported by physiological explanations. The date of mating in mink had an effect on the date of increase in plasma progesterone. Matings at a late date in the estrous period, reduced the period of delay before implantation. Nevertheless, both the dates of implantation and parturition were delayed compared with the results of earlier matings in mink. 相似文献
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Pranab L. Pakrasi 《Journal of biosciences》1997,22(2):267-271
Prostaglandins are considered to be one of the important mediators of ovum implantation. Various lipoxygenase products also have been implicated along with PGs for this process. A specific rather than preferential inhibitor of 5-lipoxygenase is used to investigate the role of leukotrienes in the event of implantation and decidualization process in mice. AA861, a selective inhibitor of 5-lipoxygenase is used in different dose levels like 50,100 and 500 μg in (A) intact pregnant mice (on D1-D4 and D2-D4 and D4); (B) delayed mice on (D3-D8); (C) pseudopregnant traumatized mice (on D1-D4). All the experimental animals of group A were killed on D6. Estrogen injected delayed animals of group  were killed 48 h after the induction of implantation. Implantation sites were counted as blue spot and compared with those of control animals. Traumatized animals of group C were killed 24 h after the mechanical traumatization and uterine weights were compared with those of vehicle treated controls. Results show that AA861 could not inhibit ovum implantation in either intact or ovariectomized delayed animals. It also did not show any adverse effect on tubal transport or development of embryos. AA861 did not have any inhibitory role on decidualization of pseudopregnant uteri also. This experiment shows that a selective inhibitor of 5-lipoxygenase enzyme may not impair the implantation in mice indicating a doubt about the involvement of 5-lipoxygenase products in implantation. 相似文献
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Isakova G. K. Zakharenko L. P. Abramova M. P. 《Russian Journal of Developmental Biology》2001,32(4):248-253
The nucleolar and extranucleolar RNA synthesis was studied in the mink blastocysts at different stages of embryonic diapause and during the periimplantation period using cytoradioautography. The data obtained suggest a differential and stage specific activity of the embryonic mRNA and rRNA synthesis during the period of delayed implantation. 相似文献
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Dr. Elizabeth G. Crichton Robert F. Seamark Philip H. Krutzsch 《Cell and tissue research》1989,258(1):183-201
Summary Developmental delay is correlated with torpor in the temperate zone bent-winged bat, Miniopterus schreibersii (latitude 37° S) as a period of pre-implantation delay (delayed implantation) followed by a short post-implantation delay (delayed development). During this time, the number of steroidogenic organelles in luteal cytoplasm is greatly reduced compared with normal embryogenesis, and granular endoplasmic reticulum is prominent. Nidation, which occurs while the animals are hibernating, is not accompanied by marked changes in luteal ultrastructure, although the number of lipid droplets decreases somewhat. Progesterone rises slightly but not significantly; however, a pre-nidation decrease in high 17-estradiol levels may play a role in implantation. Following implantation, the conceptus remains delayed at the blastocyst stage for several weeks. During this time the bats remain torpid and the only change in luteal cell ultrastructure is an increase in smooth endoplasmic reticulum as differentiation begins toward the trilaminar stage. At the end of developmental delay hypertrophy of the luteal cell begins and mitochondria and lipid droplets increase, markedly. By this time arousal from hibernation has occurred, placentation takes place, and normal development is underway. At placentation, smooth endoplasmic reticulum reaches its maximum in luteal cytoplasm; estrogen and progesterone levels peak about 6 weeks later. For the remaining 2 months of gestation, signs of luteolysis appear. These observations suggest that the corpus luteum of developmental delay, though suboptimally functional, is prolonged in its luteinization by the arrival of winter when the bats enter torpor. The capacity for maximal steroidogenesis is acquired at the end of winter, some weeks after implantation, when arousal occurs and normal development ensues. 相似文献
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哺乳动物胚胎发育产生的第一个细胞系的分离是内细胞团和滋养层的分离,不同哺乳动物之间胚胎干细胞向滋养层细胞分化不同,滋养层细胞对胚胎的植入、促进胚胎在子宫内的生存和生长至关重要.人胚胎干细胞为研究人类胚胎发育及向滋养层分化提供了一个独特的模型.人胚胎干细胞可以在实验室条件下保持无限期稳定的培养,用于最初胚胎和滋养外胚层发生的机制研究.目前人胚胎干细胞分化为滋养层细胞在体外可以通过自发分化、基因敲除、分离EB小体和BMP4诱导等几种途径实现.不同哺乳动物之间胚胎干细胞向滋养层分化机制,主要通过信号通路如BMP4,LIF等以及某些标志基因如OCT4,CDX2,Eomes等的变化调节.人胚胎干细胞向滋养层分化的研究为临床应用提供了一定的基础. 相似文献