Survival of amphibian embryos after continuous ultrasound treatment

The influence of continuous ultrasound on the embryonic development of grass frog Rana temporaria has been investigated. Intact embryos at the blastula stage were treated by ultrasound of different frequency (0.88 and 2.64 MHz), intensity (0.05-1.0 W/cm2), and duration (1-15 min). The treatment with ultrasound of frequency 0.88 MHz and intensity 0.05 W/cm2 for 1-5 min tended to increase the proportion of normally developing embryos up to hatch (10-25% of control). Increasing the intensity of ultrasound (0.88 MHz) to 0.7-1.0 W/cm2 and the duration of its action to 5-15 min induced the death of almost all of treated embryos. No significant differences were found between the development of control embryos and embryos treated with ultrasound of middle intensity (0.2-0.7 W/cm2) for 1-5 min. The exposure of amphibian embryos to ultrasound of frequency 2.64 MHz and intensity 0.05-0.7 W/cm2 for 1-5 min did not change their survival. Increasing the intensity of ultrasound (2.64 MHz) to 1.0 W/cm2 and the duration of its action to 5 min decreased the number of normal developing embryos (by 35%).     

Degradation of yolk platelets in the early amphibian embryo is regulated by fusion with late endosomes

The eggs of many animal species contain a large store of yolk platelets, lipid droplets and glycogen granules; these are consumed during early embryogenesis. However, the mechanisms by which degradation of these stored materials occurs during early embryogenesis are not clearly understood. The mechanisms underlying yolk degradation in amphibian (newt) embryos were investigated. Electron microscopy using an anion marker, cationic ferritin, revealed that yolk platelets were degraded after fusion with late endosomes containing primary lysosomes. Electron microscopy and the results of experiments using a number of reagents with selective effects on intracellular transport suggested that yolk degradation activity in early amphibian embryos may be regulated at the point of fusion between late endosomes and yolk platelets.     

Lithium induces changes in the plasma membrane protein pattern of early amphibian embryos

Summary— The plasma membrane protein pattern of Rana ridibunda embryos subjected to lithium (Li) treatment at various stages of development was examined by two-dimensional gel electrophoresis. Differences were observed at the neurula stage not only as compared to controls but among lithium-treated embryos as well. Of particular interest was the presence of proteins, specific for the gastrula stage, in lithium-treated embryos. The results are discussed in relation to the well-known effect of lithium on amphibian morphogenesis.     

A new method for the isolation of plasma membranes from amphibian embryos

Summary A method for the isolation of plasma membranes is described. N-Succinimidyl 3-(2-pyridyldithio) propionate (SPDP), a heterobifunctional reagent, is covalently linked to protein amino groups in plasma membranes of intact cells. After homogenization of the cells the plasma membranes can be separated from other cell components by selective coupling to reduced Thiopropyl-Sepharose 6B and then recovered after treatment with 2-mercaptoethanol.     

Biosynthesis of sulfated proteoglycans in amphibian embryonal cells

The synthesis of sulfated proteoglycans in small explants from various parts of late blastulae fromAmbystoma mexicanum orXenopus laevis was investigated by incorporation of radioactive sulfate or glucosamine and galactosamine in media of low, normal or high tonicity. The explants differentiated into ciliated aggregates or fibroblast-like cells, or remained undifferentiated depending upon their origin in the embryo. High tonicity induces the explants to dissociated and prevents morphological differentiation, while low tonicity hardly affects this process. Yet, both types of media decrease the incorporation into glycosaminoglycans to various degrees, ranging from 40 to 80%, depending upon the species. InXenopus, the uptake of sulfate is inhibited by as much as 90% in high tonicity media. The rate of incorporation of label is approximately twice as much in mesodermal as in animal or vegetal aggregates, which do not differ significantly. Animal aggregates fromAmbystoma, however, revealed an exceptionally high uptake of sulfate. The relative distribution of chondroitin sulfates and heparan sulfates is not affected by changes in tonicity, except inXenopus where high tonicity severely suppresses the synthesis of heparan sulfates, and is independent of the type of aggregate. The relationship between the synthesis of sulfated proteoglycans and processes involved in cell differentiation, especially cell adhesion, is discussed.     

Triploidy permits survival of an inviable amphibian hybrid

Hybrids between species frequently arrest early in development. In the frog hybrid Rana catesbeiana female × Rana clamitans male, the embryo shows a characteristic development to an exogastrula which dies. This hybrid can be rescued by pressure suppression of the second polar body, which results in the addition of another haploid set of R catesbeiana chromosomes to the embryo. The triploid hybrid expresses genes from both species and can develop normally through metamorphosis. The results show that an R catesbeiana egg containing a full haploid set of R clamitans chromosomes is capable of development and that the usual developmental arrest caused by the R clamitans genome responds to chromosomal dosage.     

Immuno-electron-microscopic study of fibronectin in gastrulating amphibian embryos

Summary The ultrastructural organization of fibronectin (FN) in early amphibian embryos (Ambystoma mexicanum, Pleurodeles waltlii) was studied with the use of antibodies directed against amphibian plasmatic FN. Scanning and transmission electron microscopy combined with immunogold labeling of FN revealed that the extracellular matrix that covers the inner surface of the ectodermal layer consists of FN-containing fibrils. During gastrulation, the mesodermal cells appear to be devoid of FN. These cells extend filopodia adhering to the FN-containing fibrils and are spreading along them. These findings suggest that FN may be involved in contact formation between mesodermal cells and the extracellular matrix that serves as a substratum for migration.     

Inducing activity of subcellular fractions from amphibian embryos

Summary The homogenate from unfertilized eggs, gastrulae, neurulae and hatched embryos ofXenopus laevis was fractionated by differential centrifugation and subsequent repeated centrifugation on discontinuous sucrose gradients. A high archencephalic-neural inducing activity was found in RNP particles, which were released from the high-speed (microsomal) sediment by treatment with EDTA, and in a fraction of heterogeneous small vesicles. The highest archencephalic inducing activity was observed in RNP particles from unfertilized eggs and from gastrulae. RNP particles isolated from hatched embryos had a lower inducing activity. The neuralizing factor can be extracted from the small vesicles with pyrophosphate buffer at pH 8.6, but it is not solubilized with a non-ionic detergent (Triton X 100). The high-speed supernatant from the gastrula homogenate contains soluble neuralizing factor, whereas the supernatant from egg homogenate has a low inducing activity. The plasma membrane fraction (isolated from gastrulae) also has only a low inducing activity. The possible significance of the subcellular distribution of neuralizing factors for the transmission of neuralizing inducer from the mesoderm to competent gastrula ectoderm and the processing of signals which are generated on the plasma membrane of induced cells is discussed.     

Inter embryonic (homo- or hetero-sexual) transfer of primordial germ cells between chicken embryos

Chicken primordial germ cells (PGCs) collected from thecirculating blood in embryonic vessels at stage 13–15 were inter-embryonically, homo- or hetero-sexually,transferred to the blood vessels of recipient embryosat the same stage of development. Approximately 30%of the embryos treated with hetero-sexual transfer of PGCs had abnormal gonads, showing ovotestis likeorgans. In this case, some of these reversed gonadswere considered to be dependent upon the ratio of thenumber of PGCs from donor to recipient embryos. Oneof the treated embryos possessed completely reversedorgans. Therefore, the introduction of exogenousembryonic vessels was thought to be also useful forproducing transgened gonads.     

Effects of temperature on developmental performance, survival and growth of sea lamprey embryos

This study assesses the influence of thermal regime on the development, survival rates and early growth of embryos of sea lamprey Petromyzon marinus incubated at five constant temperatures (7, 11, 15, 19 and 23° C). The time from fertilization to 50% hatching and from hatching to 50% burrowing were inversely related to incubation temperature. All the embryos incubated at 7° C died at very early stages, while those maintained at 11° C did not attain the burrowing stage. Survival from fertilization to hatching was 61, 89, 91 and 89% at 11, 15, 19 and 23° C, decreasing to 58, 70 and 70% from hatching to burrowing at 15, 19 and 23° C, respectively. Larvae reared during the first 3 months of exogenous feeding in a common environment at constant 21° C, revealed maximum survival for an incubation temperature of 15° C (43% of burrowed larvae) decreasing strongly at 19° C (16%) and 23° C (one suvivor among 240 larvae). Body length at the burrowing stage was maximum for embryos incubated at 19° C, but body mass increased in the interval 15–23° C. Mean incubation temperatures experienced by 117 broods during the embryonic development in the source river were estimated in 15·3±2·30° C and 16·7±1·76° C (mean±1 s.d .) for the periods fertilization-to-hatching and hatching-to burrowing, respectively.     

Synthesis and distribution of laminin-related polypeptides in early amphibian embryos

Summary Western blotting experiments carried out with several heterospecific antibodies against mouse-derived laminin allowed the identification of four laminin-related polypeptides in early Pleurodeles waltlii embryos. Synthesis of all four polypeptides was detected from the early blastula stage to late gastrula stage. Immunofluorescent staining with anti-laminin and anti-fibronectin antibodies provided evidence for a close association of these laminin-related polypeptides with the fibronectin fibrillar network.     

The microinjected Drosophila melanogaster 1731 retrotransposon is activated after the midblastula stage of the amphibian Pleurodeles waltl development

The entire 1731 retrotransposon of Drosophila melanogaster, tagged with the E. coli lac Z gene inserted in its gag sequence, was injected into oocytes and fertilized eggs of the urodele amphibian Pleurodeles waltl. Expression of the reporter gene indicated that the 1731 promoter (its 5LTR) is active in the embryos and not in the oocytes. It appeared that this element is regulated as amphibian genes are at the beginning of the development, i.e. that expression was detected after the mid blastula stage and maintained up to four or five days after injection. Another construction associating the modified 1731 promoter with the CAT gene is also expressed in Pleurodeles embryos during the same period of development. This indicated that the 1731 promoter issued from a Drosophila species is activated as promoting sequences of amphibian zygotic genes are, suggesting that in the case of horizontal transfer, 1731 can be expressed into vertebrate organisms.     

肿瘤的超声波治疗

文中就超声波热疗,高强度聚焦超声以及低频超声波在肿瘤治疗中的应用进行了描述。早期主要是利用超声波的热效应来治疗肿瘤,近年来兴起的高强度聚焦超声是热疗法的另一发展。它瞬间使肿瘤组织温度升至65℃以上,导致靶区组织凝固和坏死来达到对肿瘤的“热切除”,是一种安全、有效的肿瘤治疗手段,具有无限潜力。尽管低频超声治疗肿瘤的机制尚不明了,但因其可以诱导细胞凋亡,为肿瘤的治疗提供了新的途径,其治疗作用已受到重视。     

单个植入前胚胎mRNA差异显示方法的建立

在已有的研究基础上,优化和建立了单个植入前胚胎的mRNA差异显示（single preimplantation embryo differential display polymerase chain raction,SPEDDRT-PCR）.以小鼠单个成熟的卵母细胞和单个的2细胞期胚胎作为起始材料,比较二者之间基因的表达差异.选择在卵母细胞中不表达而在2细胞期表达的差异片段.进行GenBank检索和表达序列标签(EST)库电子克隆.与多胚研究方法一样,由线粒体编码的和2细胞特异表达的NADH脱氢酶亚单位2和ATPase 6证实了SPEDDRT-PCR方法是可行而且可靠的,是一种需要材料极少、应用广泛而有效的基因分离方法.     

Biological effects of continuous exposure of embryos and young chickens to electromagnetic fields emitted by video display units

The effects of continuous exposure of embryos and young chickens to electromagnetic fields (EMFs) emitted by video display units (VDUs) were investigated. Embryos and brood were continuously exposed during embryonic and postembryonic phases to EMFs emitted by two types of VDU (TV or computer). Embryonic mortality was evaluated in three independent experiments. Young chickens were immunized three times by porcine thyroglobulin (Tg). Blood samples were assayed after each immunization for specific anti-Tg antibodies (IgG), plasma corticosterone (CORT), and plasma melatonin (MLT). In the sham-exposed samples, embryonic death (10–33%) was restricted to the perinatal period and the IgG, CORT, and MLT responses of young chickens crested after the second immunization. Constant EMF exposure was accompanied by significantly increased fetal loss (47–68%) and markedly depressed levels of circulating anti-Tg IgG, CORT, and MLT. Collectively, these findings indicate that continuous exposure to EMFs, issuing from VDUs, adversely affects embryos and young chickens. Bioelectromagnetics 18:514–523, 1997. © 1997 Wiley-Liss, Inc.     

Harmful or Not: Trichostatin A treatment of embryos generated by ICSI or ROSI

Trichostatin A (TSA), a histone deacetylase inhibitor, is a known teratogen causing malformations such as vertebral fusions when applied during the postimplantation period; TSA also causes developmental arrest when applied during the preimplantation period. Regardless of these hindrances, we have succeeded in the establishment of an efficient somatic cloning method for the mouse where reconstructed embryos are treated with TSA. To elucidate this apparent discrepancy, we treated fertilized mouse embryos generated either by intracytoplasmic sperm injection (ICSI) or round spermatid injection (ROSI) with 50 nM TSA for 20 h after fertilization as well as parthenogenetic embryos and found that TSA treatment inhibited the preimplantation development of ICSI embryos but not ROSI or parthenogenetic embryos. And, although we often observed hypomorphism following TSA treatment in embryos grown to full term produced by both ICSI (av. of body weight: 1.7 g vs. 1.5 g) and ROSI (1.6 g vs. 1.2 g), TSA treatment reduced the offspring production rate for ICSI from 57% to 34% but not for ROSI from 30% to 36%. Thus, these data indicate that the effects, harmful or not, of TSA treatment on embryonic development depend on their nuclear derivations. Also, the resulting hypomorphism after TSA treatment is a caveat for this procedure in current Assisted Reproductive Technologies.     

Further studies on thermal treatment of two-cell stage embryos to produce complete embryonic stem-cell-derived mice by cell-aggregation methods

Employing aggregation techniques with two embryonic sources, one from two-cell stage embryos treated by thermal stimulation and the other from mouse embryonic stem (ES) cells that had been obtained from a feeder layer, simple and most effective methods of producing a complete generation of mice from ES cells were explored. Although thermal treatment affected embryos at various developmental stages, the embryos at the two-cell stage of development were selected because of the remarkably reduced number of cells present in the inner cell mass (ICM) at blastocyst stage after thermal conditioning. Under these conditions, a combination of thermally treated host embryos and an aggregated ES cell-clump was found to produce a high rate of live newborns by natural delivery. That the newborns were completely derived from ES cells was checked by two criteria: microsatellite analysis and coat color analysis. Importantly, all of these mice were healthy and fertile. The aggregation techniques reported here might well be applied to other animal species whose ES cells form stable colonies on a feeder layer.     

Embryonic loss in mares: Incidence and ultrasonic morphology

Pregnancy was determined by ultrasound on Days 11, 15, 20, 25, 30, 35, 40, 45, and 50 in 154 ponies and 27 horses. In ponies, the embryonic loss rate for Days 11 to 15 (28 154 , 18.2%) was greater (P<0.01) than for any of the subsequent five-day intervals (0% to 3.3%). There were no losses during Days 11 to 15 in horses (0 27 ), and the difference between ponies and horses was significant. The loss rates for the seven periods encompassing Days 15 to 50 were not significantly different among periods. Pseudopregnancy occurred more frequently (P<0.01) following embryonic loss after Day 20 (Days 11 to 15, 26%; Days 15 to 20, 33%; after Day 20, 100%). Embryonic vesicles that were lost during Days 11 to 15 were smaller on the average than control vesicles. However, most of the vesicles grew at an apparently normal rate. Two of five vesicles that were lost between Days 15 and 20 and three of four that were lost between Days 20 and 25 were undersized during preceding examinations. Undersized vesicles were found during 13 415 (3%) examinations during Days 11 to 20 in mares that maintained the embryo and in 21 106 (20%) in mares that lost the embryo. Embryonic vesicles that were lost during Days 11 to 15 usually disappeared without previous indications, except in three mares in which the vesicle was floating in a small collection of fluid. Ultrasonic indications of impending loss at later stages included failure of fixation, an echogenic ring (vesicle) or mass floating in a collection of fluid, an echogenic area in the dead embryo, absence of heart beat, and a gradual decrease in volume of placental fluids with disorganization of the placental membranes. The solid remnants and at least some of the fluids resulting from late embryonic and early fetal death were retained sometimes for weeks or months until the debris was apparently expelled through an open cervix.     

Conditions for a heat shock response during oogenesis and embryogenesis of the amphibian Pleurodeles waltl

The optimal conditions capable of inducing an increase in HSP70 neosynthesis during development of the urodele amphibian Pleurodeles waltl were determined in this study. These conditions depend on temperature, heat shock duration and recovery duration. In oocytes, a heat shock response was repeatedly obtained at 37°C for 15 min followed by 1 h recovery. These results provided evidence for heat shock response at every stage considered. An increase in HSP70 synthesis was noted throughout oogenesis, but it did not lead to an increase in the amount of soluble HSP70, except for stage VI oocytes. Such results suggest that from stage II to stage IV oocytes, an equilibrium occurs between the HSP70 used and the HSP70 neosynthesized. In contrast, in stage VI oocytes, heat shock led to overproduction of HSP70. During early development, the heat shock response was repeatedly obtained only from the gastrula stage with a 37°C shock and a 15min duration of treatment. Surprisingly, during cleavage stage, the soluble HSP70 total amount increased after heat shock at a time when no HSP70 neosynthesis occurred.