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The cell cycle was examined in embryo and root explants of Vicia faba in culture to test whether or not polyploidy and aneuploidy affected organogenetic potential. Nuclear DNA contents and the mitotic index were measured in the 0–1 mm apical segment of primary roots of 5-day old seedlings and at various times following transfer to modified MS in darkness or Chu's N6 medium in an 8 h light/16h dark cycle (N6-MS programme) at 20°C. Mature embryos were dissected and cut longitudinally. Each half was cultured on the N6-MS programme. Root explants grown on MS in darkness developed into callus but there was no subsequent organogenesis. Only on the N6-MS programme were new roots initiated from root-derived callus. Using the N6-MS programme, embryo-derived callus became green and after 3 to 4 months, produced roots and shoots. Approximately 40% of these cultures regenerated plantlets. Polyploidy occurred within 24 h of culture irrespective of both tissue source and culture protocol. Variations in chromosome number from 2n=2x=12 were also routinely observed. Thus, calluses had the ability to initiate roots and shoots regardless of persistent polyploidy and aneuploidy. Compared with the baseline of cell cycle data for roots in vivo, the proportions of cells in the different cell cycle phases remained constant. Thus, in V. faba induction of organogenesis seems more related to culture protocols than to specific changes to the cell cycle. The mitotic index was significantly lower in vitro compared with meristems of intact roots. 相似文献
946.
Stéphanie Foulon Tim Greacen Blandine Pasquet Romain Dugravier Thomas Sa?as Nicole Guedeney Antoine Guedeney Florence Tubach CAPEDP Study Group 《PloS one》2015,10(11)
Objective
Randomised controlled trials evaluating perinatal home-visiting programs are frequently confronted with the problem of high attrition rates. The aim of the present study is to identify predictors of study attrition in a trial evaluating a perinatal home-visiting program in France.Materials and Methods
CAPEDP is a French randomized trial comparing a perinatal home-visiting program using psychologists versus usual care (N = 440). The first assessment was at inclusion into the trial at the 27th week of pregnancy and the final assessment when the child reached the age of two. Attrition rates were calculated at 3 and 24 months postpartum. Stepwise logistic regression was used to identify predictors of early (between inclusion and 3 months postpartum) and later (between 3 and 24 months postpartum) attrition among social, psychological and parenting factors.Results
Attrition rates were 17% and 63% at 3 and 24 months respectively. At 24 months, there was significantly more attrition in the control arm (70.6%) compared to the intervention arm (55.2%). Five independent predictors of early attrition were identified: having already had an abortion; having greater attachment insecurity as measured with the Vulnerable Attachment Style Questionnaire (VASQ); having lower global severity of psychiatric symptoms as assessed with the Symptom Check-List (SCL-90) at inclusion, being neither currently employed nor studying; and declaring no tobacco consumption during pregnancy. Being randomized into the control arm, having undergone early parental loss before age 11 and having lower global severity of psychiatric symptoms (SCL-90) at 3 months postpartum were the only variables associated with later attrition.Conclusion
This study provides key information for identifying mothers who may require specific support to avoid study attrition in trials evaluating a home-visiting program. 相似文献947.
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Teichoic acids (TAs) are major wall and membrane components of most gram-positive bacteria. With few exceptions, they are polymers of glycerol-phosphate or ribitol-phosphate to which are attached glycosyl and D-alanyl ester residues. Wall TA is attached to peptidoglycan via a linkage unit, whereas lipoteichoic acid is attached to glycolipid intercalated in the membrane. Together with peptidoglycan, these polymers make up a polyanionic matrix that functions in (i) cation homeostasis; (ii) trafficking of ions, nutrients, proteins, and antibiotics; (iii) regulation of autolysins; and (iv) presentation of envelope proteins. The esterification of TAs with D-alanyl esters provides a means of modulating the net anionic charge, determining the cationic binding capacity, and displaying cations in the wall. This review addresses the structures and functions of D-alanyl-TAs, the D-alanylation system encoded by the dlt operon, and the roles of TAs in cell growth. The importance of dlt in the physiology of many organisms is illustrated by the variety of mutant phenotypes. In addition, advances in our understanding of D-alanyl ester function in virulence and host-mediated responses have been made possible through targeted mutagenesis of dlt. Studies of the mechanism of D-alanylation have identified two potential targets of antibacterial action and provided possible screening reactions for designing novel agents targeted to D-alanyl-TA synthesis. 相似文献
950.
Prof. J. Francis Hartmann Ph.D. 《Cell and tissue research》1958,48(3):291-308
Summary The fine structure of the neurohypophysis has been studied in normal and histamine-treated rats with particular reference to capillary relationships and to the neurosecretory vesicles. Certain new information on the pericapillary space has been developed and is discussed with reference to the existing literature on the posterior hypophysis and other endocrine organs. The membrane-bounded pericapillary space penetrates deeply between surrounding nerve terminals and pituicyte processes, seemingly forming a pervasive metabolic lake which undoubtedly is of physiological significance for metabolic and secretory exchange.Following histamine treatment, the neurosecretory vesicles lose their electrondense centers, the mitochondria in the nerve terminals become swollen, and the capillary endothelium shows evidence of increased pinocytosis. In one rat subjected to painful stimuli, only the first and last of the above alterations are prominent. The experimental results are interpreted in the light of previous work done by other authors, as additional evidence for the identity of the stainable neurosecretion of light microscopy and the neurosecretory vesicles of electron microscopy.The author is greatly indebted to Prof. Dr. med. W. Bargmann for the use of electron microscope facilities and for other invaluable help during the course of the work. To Frau Dr. A. Knoop of the Anatomical Institute in Kiel, and to Frl. Dr. Weichan of Siemens & Halske AG in Berlin, for aid in obtaining the micrographs, a grateful acknowledgement is extended.Presented in part at the 55th meeting of the Anatomische Gesellschaft in Frankfurt/Main, April 9–12, 1958.United States Public Health Service Special Research Fellow, on leave from Department of Anatomy, University of Minnesota Medical School, Minneapolis, Minnesota, USA. 相似文献