Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy最新文献

{"title":"Pitfalls in interpreting therapy for early pregnancy.","authors":"H J Carp","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 2","pages":"96-101"},"PeriodicalIF":0.0,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20294087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Altered expression of the tumor suppressor/oncoprotein p53 in SV40 Tag-transformed human placental trophoblast and malignant trophoblast cell lines.","authors":"G Aboagye-Mathiesen,&nbsp;M Zdravkovic,&nbsp;F D Tóth,&nbsp;C H Graham,&nbsp;P K Lala,&nbsp;P Ebbesen","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The expression of the tumor suppressor/oncoprotein p53 has been investigated in normal human placental villous trophoblast, in vitro propagated invasive extravillous trophoblast, SV40 tumor antigen (Tag)-immortalized extravillous trophoblast, human cytomegalovirus (hCMV)-infected syncytiotrophoblast and malignant trophoblast (choriocarcinoma) cell lines (JAR, JEG-3 and BeWo) using quantitative enzyme-linked immunosorbent assay (ELISA) and Western immunoblot methods using monoclonal antibodies specific for wild-type and mutant p53. The normal villous and extravillous trophoblast cells expressed low levels of the wild-type p53 protein, whereas normal terminally differentiated multinucleated syncytiotrophoblast cells, as well as hCMV-infected syncytiotrophoblast, showed a higher expression of the wild-type p53 protein. SV40 Tag-immortalized invasive trophoblast cells also showed a high expression of the wild-type p53 protein which remained complexed with the Tag protein. All the choriocarcinoma cell lines over expressed the mutant form of the p53 protein. The increased expression of p53 protein in the SV40 Tag-immortalized invasive trophoblast and choriocarcinoma cells paralleled with increased expression of the mouse double minute 2 (mdm2) oncogenic protein. Transforming growth factor (TGF)-beta inhibited proliferation of normal extravillous trophoblast cells. The antiproliferative effects of TGF-beta were reduced in SV40 Tag-immortalized cells and non-detectable in choriocarcinoma cell lines JAR, BeWo and JEG-3. The inactivation of p53 owing to complexing with Tag in the immortalized premalignant trophoblast and p53 mutation in the malignant trophoblast may be responsible for their aberrant proliferation and refractoriness to antiproliferative effects of TGF-beta observed in these cells as compared to the normal trophoblast. These results may suggest the role of p53 protein in trophoblast differentiation, transformation and tumorigenesis.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 2","pages":"102-12"},"PeriodicalIF":0.0,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20294088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Current progress in early pregnancy investigation.","authors":"B M Polliotti","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 2","pages":"136-49"},"PeriodicalIF":0.0,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20294093","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Localization of leukemia inhibitory factor in human endometrium during the menstrual cycle.","authors":"Z M Yang,&nbsp;D B Chen,&nbsp;S P Le,&nbsp;R W Brown,&nbsp;C J Chuong,&nbsp;M J Harper","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Leukemia inhibitory factor (LIF) has been shown to be imperative for the implantation of mouse blastocysts. The objective of this study was to examine the pattern of LIF protein in the human endometrium during the menstrual cycle. A low level of LIF was detected in endometrial glands during the proliferative phase. During the luteal phase, LIF staining in the glands appeared stronger in the mid- and late luteal phase than immediately after ovulation. However, a low level of LIF was detected in the stromal cells during the early and midproliferative phase, while only a minimal level was observed during the late proliferative and luteal phases.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"18-22"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20292842","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Differential effects of plasma from normal and ectopic gestation on lymphocyte proliferation.","authors":"T A Nasser,&nbsp;K A Hansen,&nbsp;R E Ratzlaff","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>This study investigated immunoregulatory differences as a result of anatomical changes in the fetomaternal interface. Thirty-one female subjects were recruited from a military tertiary-care facility. Ten subjects were non-pregnant while 21 were pregnant (nine normal and 12 ectopic gestations). Immune tests included one-way mixed lymphocyte cultures with and without maternal plasma, phytohemagglutinin stimulation and lymphocyte phenotypes. Basic statistics and a one-way ANOVA using Tuckey's HSD model were employed. Autologous plasma significantly enhanced the allogeneic responses of first-trimester pregnant females with normal gestations to spouses as well as to control male lymphocytes. This enhancement was not observed in either ectopically-pregnant or non-pregnant subjects. Mitogen stimulation and lymphocyte populations were similar in all three groups. The first trimester of normal pregnancy is characterized by the presence of soluble intrauterine pregnancy-specific lymphocyte-enhancing factors. Ectopic gestation lacks this phenomenon.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"23-8"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20292843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Current progress in early pregnancy investigation.","authors":"B M Polliotti","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"43-52"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20294083","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Comparison of production of choriogonadotropin inhibitory protein, prolactin and insulin-like growth factor binding protein-1 by human decidua in vitro.","authors":"S G Ren,&nbsp;G D Braunstein","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>We have previously demonstrated that human decidua produces a protein (decidual choriogonadotropin inhibitory protein, DCIP) that inhibits human chorionic gonadotropin (hCG) secretion from primary trophoblasts and JEG-3 choriocarcinoma cells. The present study was undertaken to examine the relationship of DCIP production to that of cell protein, prolactin (PRL) and insulin-like growth factor binding protein-1 (IGFBP-1). Term decidual cells, isolated from placental membranes by enzyme digestion and density gradient centrifugation, were incubated for 12 days in serum-free CMRL-1066 medium which was changed daily. At the end of each experiment the DCIP in the decidual culture medium was measured by bioassay: the percentage reduction, from control, of hCG production by JEG-3 cells exposed to 30% DCIP-containing decidual culture medium. Prolactin, IGFBP-1 and hCG were measured by radioimmunoassay. The DCIP activity was maximal during the first 3 days in culture. The bioactivity of decidual culture medium collected after the 5th day of culture gradually decreased and medium obtained from the final day of culture actually stimulated hCG secretion in the bioassay. Decidual cell protein gradually declined from 100% on day 1 to 56% on the last day of culture. The concentrations of protein, PRL and IGFBP-1 in the decidual culture medium gradually decreased during the first 4-6 days, followed by a rise. In contrast, glucose increased with time in culture. Production of PRL, IGFBP-1 and decidual culture medium protein exhibited a significant quadratic effect over the 12 days in culture. There was a negative relationship between decidual cell protein and glucose (r = -0.95) and a positive correlation between cell protein and protein in the decidual culture medium (r = 0.58). The DCIP activity was related to cell protein (r = 0.39), protein concentration in decidual culture medium (r = 0.36), and inversely related to the glucose level (r = -0.41). There was no relationship between DCIP activity and PRL or IGFBP-1. These results indicate that maximal DCIP production occurs during the first several days in short-term culture of decidual cells and is related to decidual-cell viability. As decidual-cell viability decreases, there is less glucose consumption in the decidual culture medium and the higher glucose levels may be responsible for the stimulatory effect of medium collected at the end of the study on JEG-3 hCG secretion.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"36-42"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20294082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Cell adhesion, cell adhesion molecules and their functional role in the human endometrium.","authors":"P J van der Linden","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In summary, cadherins are important determinants of tissue morphology. They play a major role in the maintenance of intercellular junctions in normal epithelial cells in most organs. Cadherin expression is found to be perturbed in human invasive carcinoma. Cadherins are probably crucial for many other morphogenetic processes which involve selective cell adhesion or detachment. Expression of integrins allows binding of endometrial cells to various ligands (fibronectin, laminin, collagens) and hence adds to the preservation of the architectural integrity of endometrium. Regulation of adhesion-molecule expression probably contributes to the invasive behavior of cytotrophoblast, both in physiological and pathophysiological conditions. The integrin expression by the endometrium seems to be a dynamic process, many details of which still remain to be elucidated.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"5-14"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20292840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A meta-analysis of perinatal complications of maternal diabetes. Can they be prevented?","authors":"M Hod,&nbsp;P Merlob","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"15-7"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20292841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Comparative responsiveness to prolonged hyperinsulinemia between adipose-tissue and mammary-gland lipoprotein lipase activities in pregnant rats.","authors":"P Ramos,&nbsp;E Herrera","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The present study was addressed to determining the comparative responsiveness of lipoprotein lipase (LPL) activity, in white adipose tissue and mammary gland, to a prolonged hyperinsulinemic stimulus, in pregnant and virgin rats. Pregnant rats at the 17th day of gestation and virgin animals were subjected, under conscious and unrestrained conditions, to a continuous infusion with either 50% glucose or double-distilled water (controls) (35 ml/day) for 72 h through a catheter in the jugular vein. The basal plasma-glucose levels were lower in pregnant than in virgin rats. After the glucose infusion plasma-glucose levels remained unchanged but plasma-insulin levels were much higher, and this effect was greater in pregnant than in virgin rats. Whereas LPL activity in white adipose tissue in the controls was lower in pregnant than in virgin rats, in rats receiving the glucose infusion it increased more in pregnant than in virgin rats. However, LPL activity in the mammary gland was already higher in control pregnant rats than in virgin controls and the glucose infusion caused a similar increase in both groups. Although there was a linear correlation when individual values, from all the studied rats, for LPL activity in both tissues were plotted against plasma insulin levels, the correlation coefficient was much higher for mammary-gland LPL activity than for adipose-tissue LPL activity. Plasma-triglyceride levels were higher in pregnant than in virgin rats. The glucose infusion did not modify this parameter, probably because of the changes in LPL activity in other tissues which are known to occur in the opposite direction to those observed in this study for adipose tissue and mammary gland. The present results support the notion that the insulin resistant condition which normally occurs during late gestation is responsible for the decreased LPL activity in adipose tissue, but that the mammary gland remains sensitive to insulin and so maternal hyperinsulinemia would contribute to the induction of LPL activity in this organ prior to parturition.</p>","PeriodicalId":11444,"journal":{"name":"Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy","volume":"2 1","pages":"29-35"},"PeriodicalIF":0.0,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20292844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}