着床与生长因子的关系研究进展

论述了着床的生理机制。同时介绍了EGF、TGF、KGF和PDGF等生长因子对着床的调控作用。     

水稻耐盐机理的研究Ⅲ.不同基因型对NaCl吸收和运转的动力学比较

本文应用动力学研究方法比较了具有不同耐盐性的3组共6个水稻基因型对NaCl吸收和运转的差异,结果表明,在外部低NaCl浓度(0.1mmolL~(-1)时,水稻对Na~+的吸收为被动吸收,耐盐基因型对Na~+的吸收速率显著低于盐敏感基因型;对Cl~-的吸收为主动吸收,不同耐盐性基因型吸收Cl~-的动力学参数(V_(?)、K_(?))差异不显著,在外部高NaCl浓度(50mmolL~(-1))时,耐盐基因型对Na~+和cl~-的吸收速率均低于对应的盐敏感基因型。耐盐基因型水稻的Na~+、cl-从根部向地上部的运转率低于对应的盐敏感基因型,这种差异在高盐浓度时更为明显。表明了耐盐基因型水稻地上部对NaCl的排斥作用是吸收控制和运转控制共同作用的结果,使地上部Na~+、Cl-含量相对降低而显出较高的耐盐性。     

碳酸氢根和铵态氮共同对菜豆生长及养分吸收的影响

 以菜豆为材料进行水培试验, 探讨了高浓度NH₄⁺-N与HCO₃^-共存介质对菜豆生长发育及其营养吸收的影响, 结果表明: ①以HCO₃^--N 为主要氮源时, 菜豆生长状况最好; 以NH₄⁺-N为主要氮源且无HCO₃^-存在时, 培养前期菜豆根系就发生受害现象, 叶片出现萎蔫; 但加入HCO₃^-后, 随着营养液中HCO3- 浓度从0 升高到13. 0 mmol/L , 菜豆长势逐渐改善, 表明HCO₃^-与NH4+ 以较合适的比例共存于介质中可明显减轻二者非共存对菜豆生长的抑制作用。② 同一处理, 菜豆整株对主要营养元素吸收量的次序为: N > K> P > Ca >Mg > Fe >Mn , 以NH4+2N 为主要氮源时, 随HCO₃^-浓度升高, 菜豆对N、P、Ca、Mn 的吸收量逐渐增大。③以NO_3^--N 为主要氮源, P、Fe、Mn 元素在根部出现累积, 而以NH₄⁺-N为主要氮源时, 随HCO₃^-浓度增加, N、P、Ca、Mn 在根部亦有累积现象。     

Chloride channels of platelets

Chloride channels distribute widely in the body, and participate in many physiological actions and regulatory processes. Based on their physiological roles and molecular structures, six kinds of chloride channels have been identified: (1) The chloride channels family; (2) Cystic fibrosis transmembrane conductance regulator; (3) Swelling-activated chloride channels; (4) Calcium-activated chloride channels; (5) The p64 (CLIC) gene family; (6) γ-aminobutyric acid and glycine receptors. The chloride channels do exist in platelets, and their appearances are dependent on the presence of intracellular calcium. Blocking agents of chloride channels inhibit the thrombin-activated platelet aggregation and the elevation of the intracellular calcium concentration in a dose-dependent manner. It is suggested that chloride channels play a role in the activation of platelets. In addition, chloride channels act on both the cell volume regulation and the intracellular pH regulation in platelets.     

Differential gene expression of Eph‐ephrin A1 and LEPR‐LEP with high or low number of embryos in pigs during implantation

The objective of this study was to ascertain whether mRNA and protein expressions of implantation‐related genes (erythropoietin‐producing hepatocellular receptor–ligand A1, Eph‐ephrin A1 and leptin receptor–leptin, LEPR‐LEP) differed between pigs with high and low number of embryos, and whether these differences in gene expression might affect embryo implantation. Experimental pig groups (n = 24) for high and low number of embryos were prepared by altering the number of eggs ovulated in pre‐pubertal gilts treated with 1.5 × (High) or 1.0 × (Low) PG600 ([400 IU PMSG + 200 IU hCG]/dose, AKZO‐NOBEL). Gilts expressing oestrus were artificially inseminated twice and maintained in breeding and gestation until the reproductive tract was collected on day 22 of pregnancy. At slaughter, the reproductive tracts from each pregnant gilt from each treatment were immediately processed to collect samples for RNA and protein analysis. Within each gilt, three conceptus points were sampled, one from each horn and then a random conceptus within the tract. At each conceptus point, endometrial attachment site, chorion–allantois and embryo were collected and immediately frozen in liquid nitrogen. Number of corpus luteum (CL) (35.4 vs. 12.6) and total embryo number (18.8 vs. 10.2) were greater in the high‐embryo compared to the low‐embryo group, respectively (p < .05). Real‐time qPCR results showed that Eph‐ephrin A1 mRNA expression was less in the high‐embryo (p < .05) compared to the low‐embryo group. In addition, Western blotting analysis indicated that Eph‐ephrin A1 and LEP protein expression at endometrial attachment site in high‐embryo was less (p < .05) compared to low‐embryo group. It was also noted that mRNA expression of Eph‐ephrin A1 and LEPR‐LEP was greater in pregnant than non‐pregnant gilts (p < .05). Moreover, mRNA expression of Eph‐ephrin A1 (p < .05) and LEPR‐LEP was greatest at endometrial attachment site among all three tissues. There was a positive correlation between expressions of Eph‐ephrin A1, LEPR‐LEP and embryo length with the correlation coefficient 0.31–0.59. For Eph‐ephrin A1, the highest correlation coefficient appeared between Eph A1 expression and normal embryo number, between ephrin A1 expression and embryo length. For LEPR‐LEP, the highest correlation coefficient appeared between LEPR‐LEP expression and ovary weight (0.79 for both, p < .05), followed by embryo length and weight. The results of this study suggest that low expression of Eph‐ephrin A1 and LEPR‐LEP is somehow related to increased embryo number during implantation and that endometrial attachment site might be the main target tissue of these gene products. Yet, the increased expression of Eph‐ephrin A1 and LEPR‐LEP appeared associated with increased embryo growth (length and weight) and ovary weight, Eph‐ephrin A1 and LEPR‐LEP might play roles in the regulation of embryo implantation in pigs.     

重组白细胞介素-2高效纯化方法建立

依次通过离子交换法、凝胶过滤法纯化重组白细胞介素-2(IL-2)粗品,利用SDS-PAGE电泳和hIL-2 Elisa kit检测纯化后重组IL-2的纯度和浓度。结果表明,纯化后的重组IL-2纯度和浓度高。本纯化方法简单、稳定、纯化效果好,可为重组IL-2的生产工艺提供技术支持和依据。     

潮州6种蔬菜汤中F~-·Cl~-·NO_2~-·NO_3~-的同时测定

[目的]同时测定潮州蔬菜汤中F-、Cl-、NO2-和NO3-的含量。[方法]利用WICⅡ-型离子色谱仪,测定潮州不同鲜度6种蔬菜汤中F-、Cl-、NO2-和NO3-的的含量。[结果]菜汤中NO3-的含量较高;菜汤中有适宜的F-、Cl-含量。[结论]保鲜处理放置的蔬菜中,NO2-、NO3-含量增加。     

Evaluation of Commercial Fe(III)‐Chelates Using Different Methods

Abstract

A collaborative assay among three laboratories was made in order to compare both the ion (CEN. EN 13368‐2:2001 E. Determination of chelating agents in fertilizers by ion chromatography. Part 2: EDDHA and EDDHMA, 2001a) and the ion‐pair (Lucena, J.J.; Barak, P.; Hernandez‐Apaolaza, L. Isocratic ion‐pair high‐performance liquid chromatographic method for the determination of various iron(III) chelates. J. Chromatogr. A 1996, 727, 253–264) high performance liquid chromatography (HPLC) methods as well as the soluble and complexed Fe (CEN. EN 13366:2001 E. Treatment with a cation exchange resin for the determination of the chelated micronutrient content and of the chelated fraction of micronutrients, 2001b) methods. Fifteen and ten samples of commercial fertilizers of Fe‐EDDHA, Fe‐EDDHMA, respectively were analysed by three laboratories using these methods. No significant differences were observed between the results obtained for the Fe‐EDDHA content using the Lucena et al. or CEN method. The first method makes it possible to distinguish between the meso and DL‐racemic diasteroisomers of Fe‐o, o‐EDDHA. For the Fe‐EDDHMA formulations, the CEN method gives higher values than the ion‐pair method, since in the first one Fe‐EDDH4,6MA coelutes with FeEDDHMA. Also the CEN method does not makes it possible to distinguish between Fe‐EDDHMA and Fe‐EDDH5MA products. The variability among laboratories was larger for the CEN method than for the Lucena et al. method.     

A novel mutation of the CLCN1 gene associated with myotonia hereditaria in an Australian cattle dog

BACKGROUND: Heritable myotonia is a genetic muscle disorder characterized by slow relaxation of skeletal muscles. The main clinical signs are skeletal muscle stiffness, especially after vigorous contraction, and muscle hypertrophy. Muscle stiffness may be enhanced by inactivity, and often is relieved by exercise. Myotonia can be inherited in an autosomal dominant or recessive manner (Thomsen- or Becker-type myotonia, respectively). In mice, goats, Miniature Schnauzer dogs, and most affected humans, the disorder is caused by mutations in CLCN1, which encodes the skeletal muscle voltage-gated chloride channel, Cl1C-1. HYPOTHESIS: We hypothesized that an Australian Cattle Dog with generalized muscle stiffness and hypertrophy examined at the Ontario Veterinary College would have a mutation in the CLCN1 gene. ANIMALS: A pure-bred Australian Cattle Dog from Ontario, Canada, was used. METHODS: Based on clinical signs and electromyographic test results, a diagnosis of myotonia hereditaria was made, and a muscle biopsy was collected for genetic analysis. RESULTS: Sequence data obtained from the affected dog confirmed that it was homozygous for a single base insertion in the CLCN1 coding sequence. This mutation would result in a truncated ClC-1 protein being expressed, which, based on molecular evidence from other studies, would result in functionally compromised chloride conduction in the skeletal muscles of the animal. CONCLUSIONS AND CLINICAL IMPORTANCE: To the authors' knowledge, this report describes the Ist case of myotonia in an Australian Cattle Dog and represents the 1st non-Schnauzer canine myotonia to be genetically characterized. In addition, we developed a polymerase chain reaction-based genetic screen to detect heterozygotes with this mutation in the at-large Australian Cattle Dog population.