Why Eberl is wrong. Reflections on the beginning of personhood

In a paper published in Bioethics, Jason Eberl has argued that early embryos are not persons and should not be granted the status possessed by them. Eberl bases this position upon the following claims: (1) The early embryo has a passive potentiality for development into a person. (2) The early embryo has not established both 'unique genetic identity' and 'ongoing ontological identity', which are necessary conditions for ensoulment. (3) The early embryo has a low probability of developing into a more developed embryo. This paper examines these claims. I argue against (1) that a plausible view is that the early embryo has an active potentiality to grow into a more developed embryo. Against (2), I argue that neither 'unique genetic identity' nor 'ongoing ontological identity' are necessary conditions for ensoulment, and that 'ongoing ontological identity' is established between early embryos and more developed embryos. Against (3), I argue that the fact that the early embryo has a low probability of developing into a more developed embryo, if true, does not warrant the conclusion that the early embryo is not a person. If Eberl is right that the human soul is that which organises the activities of a human being and that ensouled humans are persons, embryos are persons from conception.     

猕猴早期胚胎脑的发育与凋亡相关蛋白P53的表达

目的探讨猕猴早期胚胎脑的发育及细胞凋亡相关蛋白P53的表达.方法建立猕猴早孕模型,获取早期胚胎,采用单克隆抗体链霉素亲生物蛋白过氧化酶 (SP)免疫组织化学方法,检测P53蛋白的表达.结果在猕猴25d、40d和55d胚胎脑均检测到P53免疫反应阳性神经细胞,随着胎龄的增加,P53免疫反应阳性表达率逐渐增大.结论在早期猕猴胚胎脑发育的不同时期内P53蛋白均有表达,并在胚胎脑发育过程中表达逐渐增加,调控脑的发育.     

Interferon synthesis in the early post-implantation mouse embryo

Abstract. A qualitative bioassay was adapted and used to determine the ability of the early post-implantation mouse embryo to synthesise interferon. Interferon production was not seen in any embryo tissue in the absence of an inducer and could only be detected in virus-induced tissue from the early 7th day of development. This induced interferon synthesis was initially confined to the trophoblast of the early 7th day embryo. It was then found in tissues of both trophoblast and inner cell mass origin in the early 8th day, and subsequently, in derivatives of the embryonic ectoderm in the 13th-day embryo.     

Interferon synthesis in the early post-implantation mouse embryo

A qualitative bioassay was adapted and used to determine the ability of the early post-implantation mouse embryo to synthesise interferon. Interferon production was not seen in any embryo tissue in the absence of an inducer and could only be detected in virus-induced tissue from the early 7th day of development. This induced interferon synthesis was initially confined to the trophoblast of the early 7th day embryo. It was then found in tissues of both trophoblast and inner cell mass origin in the early 8th day, and subsequently, in derivatives of the embryonic ectoderm in the 13th-day embryo.     

Early embryo‐maternal communication in the oviduct: A review

An intact embryo‐maternal communication is critical for the establishment of a successful pregnancy. To date, a huge number of studies have been performed describing the complex process of embryo‐maternal signaling within the uterus. However, recent studies indicate that the early embryo communicates with the oviductal cells shortly after fertilizationand that this is important for the successful establishment of pregnancy. Only if the early embryo is capable to signal the mother within a precise timeframe and to garner a response, will the embryo be able to survive and reach the uterus. This review will give an overview of all the experimental designs which have investigated embryo‐maternal interaction in the oviduct. In addition to that, it will provide a comprehensive analysis of the findings to date elucidating the morphological and molecular changes in the oviduct which are induced by the presence of the early embryo highlighting how the tubal responses affect embryo development and survival.     

Subzonal older adult fibroblast insertion in both in vivo-fertilized and nuclear transfer rabbit zygotes and embryos: effects on further in vitro embryo development

In the present work, we evaluated the effect on further in vitro embryo development of inserting rabbit adult fibroblasts into in vivo-fertilized rabbit embryos. To this end, we inserted either 4 or 15-20 rabbit adult fibroblasts in two different early embryo stages of development, 1-cell stage and 4-8-cell stage embryos. We observed that fibroblast insertion not only did not negatively affect further embryo development, but also may have exerted a positive effect on development on it. Therefore, in forthcoming works were where we intend to study a possible cell helper role on early embryo development. The early embryo microenvironment may reprogram somatic cell gene expression of fibroblasts inserted within the embryo, making them suitable as nuclear donors.     

Antioxidants and total oxyradical scavenging capacity during grass shrimp, Palaemonetes pugio, embryogenesis

During embryogenesis in grass shrimp the capacity to scavenge oxyradicals increased as measured by the Total Oxyradical Scavenging Capacity (TOSC) assay. The increase in TOSC during embryogenesis was associated with increasing concentrations of a number of antioxidants, including coenzyme Q (ubiquinone), alpha-tocopherol and reduced glutathione. Glutathione concentrations ranged from 0.004 to 0.005 nmol/embryo in early embryo stages and reached concentrations between 0.16 to 0.23 nmol/embryo in late embryo stages. Ascorbate remained essentially constant (0.16-0.20 nmol/embryo) throughout embryogenesis and may provide the preponderance of TOSC during early embryo development. Carotenoids were associated with yolk lipovitellin and these antioxidants decreased as yolk was absorbed during embryogenesis. Astaxanthin and beta-carotene were identified in embryos with astaxanthin always the principal carotenoid. In early embryo stages there are maternally derived antioxidants but as embryogenesis proceeds there is an assembly of a complex antioxidant system by newly formed cells and tissues.     

Effect of progesterone on embryo survival

Increased genetic selection over the past 40 years has resulted in a dairy cow with an improved biological efficiency for producing milk but with an associated reduced fertility. Embryo loss is the greatest factor contributing to the failure of a cow to conceive. The extent and timing of embryo loss indicates that 70% to 80% of this loss occurs in the first 2 weeks after artificial insemination (AI). This is the period when a number of critical phases in embryo development occur and where protein accretion, substrate utilization and embryo metabolism increase dramatically. During this time the early embryo is completely dependent on the oviduct and uterine environment for its survival and it is likely that the embryo requires an optimal uterine environment to ensure normal growth and viability. There is increasing evidence of an association between the concentration of systemic progesterone and early embryo loss and that progesterone supplementation of cows, particularly those with low progesterone, can reduce this loss. While progesterone is known to affect uterine function and embryo growth, little is known about the uterus during the period of early embryo loss and how this is affected by changes in the concentration of systemic progesterone. The expression of uterine genes encoding the transport protein retinol binding protein (RBP) and the gene for folate binding protein (FBP) appear to be sensitive to changes in systemic progesterone, particularly during the early luteal phase of the cycle. Uterine concentrations of proteins also seem to be regulated by stage of cycle; however, their relationship with the systemic concentration of progesterone is unclear. There is an urgent need to characterize the uterine environment from a functional perspective during the early part of the luteal phase of the cycle, particularly in the high-producing cow, in order to understand the factors contributing to early embryo loss and in order to devise strategies to minimize or reduce this loss.     

哺乳动物早期胚胎体外发育阻滞的研究进展

哺乳动物胚胎在体外培养中普遍存在早期发育阻滞的现象。对此,人们用形态学、生物化学、分子生物学、显微操作等手段开展了磷酸、葡萄糖、次黄嘌呤和细胞质因素对早期胚胎发育阻滞的影响的研究。本综合分析了共培养系统的优缺点。说明了采用完全成分已知的培养液对进行有关研究的必要性。列出了有效运用于克服小鼠、大鼠、仓鼠、兔、猪、羊、牛、猴等动物早期胚胎阻滞的成分知的培养液的名称。     

ART患者早期流产组织染色体异常及相关因素分析

目的:分析ART患者早期流产组织染色体异常及其相关影响因素。方法:回顾性分析2013-2017年ART患者行早期流产组织染色体检查的409例样本,分析胚胎染色体非整倍性发生及其与女方年龄、不孕年限、不孕因素、促排卵指标之间的关系。结果:ART流产患者中,流产组织染色体非整倍性发生率为57.46%,发生频次以16三体占比最高(23.95%),其次是22三体(13.45%)及Turner(9.24%)。流产组织染色体非整倍性患者平均年龄高于染色体整倍性患者(P0.001)。16三体组患者年龄低于22三体(P0.01)及Turner组(P0.05)。16三体组患者平均Gn使用量低于22三体组(P0.05)。16三体组患者移植15天血HCG值低于22三体(P0.05)及Turner组(P0.01)。结论:ART患者流产组织染色体非整倍性与女方年龄正相关,但16三体及Turner的发生与女方年龄相关性不大,且16三体更容易引发早期流产。     

Translational repression of a C. elegans Notch mRNA by the STAR/KH domain protein GLD-1

In C. elegans, the Notch receptor GLP-1 is localized within the germline and early embryo by translational control of glp-1 mRNA. RNA elements in the glp-1 3'untranslated region (3' UTR) are necessary for repression of glp-1 translation in germ cells, and for localization of translation to anterior cells of the early embryo. The direct regulators of glp-1 mRNA are not known. Here, we show that a 34 nucleotide region of the glp-1 3' UTR contains two regulatory elements, an element that represses translation in germ cells and posterior cells of the early embryo, and an element that inhibits repressor activity to promote translation in the embryo. Furthermore, we show that the STAR/KH domain protein GLD-1 binds directly and specifically to the repressor element. Depletion of GLD-1 activity by RNA interference causes loss of endogenous glp-1 mRNA repression in early meiotic germ cells, and in posterior cells of the early embryo. Therefore, GLD-1 is a direct repressor of glp-1 translation at two developmental stages. These results suggest a new function for GLD-1 in regulating early embryonic asymmetry. Furthermore, these observations indicate that precise control of GLD-1 activity by other regulatory factors is important to localize this Notch receptor, and contributes to the spatial organization of Notch signaling.     

达氏鳇不同发育期胚胎对低温的耐受研究

研究了达氏鳇12个发育期胚胎经过不同低温（2 ℃、3 ℃、5 ℃、7 ℃和8 ℃）处理12 h、24 h、2 d、3 d、6 d、10 d、15 d、20 d和30 d后的孵化率和仔鱼成活率.结果表明,卵黄栓期、隙状胚孔期、神经管闭合期胚胎在2～8 ℃水温下,处理24 h后孵化率为0;卵裂期、囊胚早期、原肠中期胚胎在2～8 ℃水温下,处理3 d后孵化率低于30%;囊胚晚期、原肠早期、眼基期、尾芽期、心跳期和尾达头部期胚胎在5～8 ℃水温下,处理3 d后孵化率、仔鱼成活率超过70%;随低温处理时间延长,胚胎和仔鱼的死亡率增加,处理时间与孵化率、仔鱼成活率呈负相关;囊胚晚期、原肠早期、眼基期胚胎在5 ℃水温下耐受力较强,处理10 d后孵化率、仔鱼成活率超过70%.本研究表明,达氏鳇胚胎发育过程中囊胚晚期、原肠早期和眼基期胚胎可以在某一低温下进行短期保存,其孵化率、仔鱼成活率与常温（16～17 ℃）下没有显著差异.这对于达氏鳇胚胎（受精卵）的长途运输有重要意义.     

Changes in Activities of Enzymes of Nitrogen Metabolism in Seedcoats and Cotyledons during Embryo Development in Pea Seeds

In the seedcoats of developing pea seeds, the maximal activities of asparaginase (EC 3.5.1.1) and aspartate: α-ketoglutarate aminotransferase (EC 2.6.1.1) are attained early in development, before the embryo has expanded to fill the embryo sac. These two enzyme activities could account for the early absence of asparagine and aspartate from the fluid secreted by the seedcoats into the embryo sac.     

Anatomical Studies of After-Ripening of Coptis chinensis Seed

The seeds of Coptis chinensis Franeh took 9–10 months to germinate after they were collected and buried under ground.. This is due to the fact that the embryo of Coptis chinensis was not fully developed after shedding but remained in the stage of globular or early heart-shaped embryo, and the latter of which has to pass through a rather long period before it developed into torpedo-embryo stage. Embryo completed its growth about January of the following year. The delay in seed germination is because of the embryo not being fully developed after shedding. However, the primordium of the first foliage leaf initiated early in the apical meristem of the young embryo. Perceiving the whole process of the young embryo growth, it seems possible that, if a suitable condition is envisaged to shorten the heart-shaped embryo stage, the whole germinating process of seed might be somewhat curtailed.     

Involvement of LIMK1/2 in actin assembly during mouse embryo development

LIMKs (LIMK1 and LIMK2) are serine/threonine protein kinases that involve in various cellular activities such as cell migration, morphogenesis and cytokinesis. However, its roles during mammalian early embryo development are still unclear. In the present study, we disrupted LIMK1/2 activity to explore the functions of LIMK1/2 during mouse early embryo development. We found that p-LIMK1/2 mainly located at the cortex of each blastomeres from 2-cell to 8-cell stage, and p-LIMK1/2 also expressed at morula and blastocyst stage in mouse embryos. Inhibition of LIMK1/2 activity by LIMKi 3 (BMS-5) at the zygote stage caused the failure of embryo early cleavage, and the disruption of LIMK1/2 activity at 8-cell stage caused the defects of embryo compaction and blastocyst formation. Fluorescence staining and intensity analysis results demonstrated that the inhibition of LIMK1/2 activity caused aberrant cortex actin expression and the decrease of phosphorylated cofilin in mouse embryos. Taken together, we identified LIMK1/2 as an important regulator for cofilin phosphorylation and actin assembly during mouse early embryo development.     

Auxin Control of Embryo Patterning

Plants start their life as a single cell, which, during the process of embryogenesis, is transformed into a mature embryo with all organs necessary to support further growth and development. Therefore, each basic cell type is first specified in the early embryo, making this stage of development excellently suited to study mechanisms of coordinated cell specification—pattern formation. In recent years, it has emerged that the plant hormone auxin plays a prominent role in embryo development. Most pattern formation steps in the early Arabidopsis embryo depend on auxin biosynthesis, transport, and response. In this article, we describe those embryo patterning steps that involve auxin activity, and we review recent data that shed light on the molecular mechanisms of auxin action during this phase of plant development.     

Nutrition, synchronization, and management of beef embryo transfer recipients

A commercially viable cattle embryo transfer industry was established during the early 1970s. Initially, techniques for transferring cattle embryos were exclusively surgical. However, by the early 1980s, most embryos were transferred nonsurgically. For an embryo transfer program to be effective, numerous factors need to be in place to ensure success. Nutrition, estrous cycle control, and recipient management are all responsible for the success or failure in fertility for a given herd. Utilization of body condition scores is a practical method to determine nutritional status of the recipient herd. Prepartum nutrition is critical to ensure that cows calve in adequate body condition to reinitiate postpartum estrous cycles early enough to respond to synchronization protocols. Estrus synchronization for embryo transfer after detected estrus or for fixed-time embryo transfer without estrus detection are effective methods to increase the number of calves produced by embryo transfer. In addition, resynchronization of nonpregnant recipients effectively ensures that a high percentage of recipients will return to estrus during a 72 h interval and are eligible for subsequent embryo transfers. Numerous additional factors need to be assessed to ensure that the recipient herd achieves its reproductive potential. These factors include assessing the merits of nulliparous, primiparous, or multiparous cows, ensuring that facilities allow for minimal stress, and that the herd health program is well-defined and followed. Numerous short- and long-term factors contribute to recipients conceiving to a transferred embryo, maintaining the embryo/fetus to term, delivering the calf without assistance and raising and weaning a healthy calf.