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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Annals of hematology 41 (1980), S. 119-130 
    ISSN: 1432-0584
    Schlagwort(e): Nucleus ; Nuclear protein ; Histone ; Granulocyte ; Leukocyte ; Nuklearproteine ; Histone ; Granulozyten ; Leukozyten
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Beschreibung / Inhaltsverzeichnis: Summary Alterations in nuclear proteins during maturation may be responsible for gene activation and repression. Study of these proteins requires: (1) a system for separating cells into varying degrees of maturity, and (2) a procedure for separating the nuclear proteins. The former was accomplished using Ficoll/Hypaque density gradients to separate rabbit granulocyte precursors. Erythrocytes and their precursors were removed by hypotonic lysis. Histones were extracted from purified nuclei with sulfuric acid, and analyzed on polyacrylamide gels containing urea. Residual non-histone proteins were separated by electrophoresis on sodium dodecyl sulfate-polyacrylamide gels. Quantitation of nuclear proteins during development shows no change in the histones, but a significant increase in the non-histone proteins. Therefore, the ratio of non-histone to histones increases progressively during maturation. Histone electrophoresis revealed no significant qualitative or quantitative changes in their five major classes during development. By contrast, electrophoretic analysis of the non-histone proteins revealed distinct changes which include a striking decrease in low molecular weight protein during maturation, and also certain changes in other peptide bands. These changes may reflect alterations in nuclear structure, a changing complement of the nuclear proteins involved in genetic regulation, or a combination of both.
    Notizen: Zusammenfassung Veränderungen der Kernproteine während der Zellreifung können für die Gen-Aktivierung und -Repression verantwortlich sein. Eine Untersuchung dieser Proteine erfordert: 1. Ein System zur Separierung von Zellen verschiedener Reifestufen; 2. eine Methode zur Separierung der Kernproteine. Das erstere wurde durch Separation von granulozytären Vorläuferzellen des Kaninchens im Ficoll-Hypaque-Dichtegradienten erreicht; hierbei wurden Erythrozyten und ihre Vorläufer durch hypotone Lyse entfernt. Sodann wurden Histone aus gereinigten Kernextrakten durch Schwefelsäure extrahiert und auf harnstoffhaltigem Polyacrylamid-Gel analysiert. Die restlichen Proteine wurden elektrophoretisch auf Polyacrylamid-Gel getrennt. Während der Zellentwicklung zeigen die Kernproteine keine quantitativen Änderungen der Histone, jedoch eine signifikante Zunahme der Nicht-Histon-Proteine. Das Verhältnis von Nicht-Histonen zu Histonen nimmt deshalb während der Zellreifung ständig zu. Die Histon-Elektrophorese deckte keine signifikanten oder quantitativen Veränderungen in den fünf Hauptgruppen während der Reifung auf. Im Gegensatz hierzu zeigte die elektrophoretische Analyse der Nicht-Histon-Proteine deutliche Veränderungen, wie z.B. eine wesentliche Abnahme der niedrigmolekularen Proteine während der Reifung und bestimmte Veränderungen in anderen Peptidbanden. Diese Befunde können Veränderungen in der Kernstruktur oder einen wechselnden Anteil an Kernproteinen der genetischen Regulation bzw. beides widerspiegeln.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Cell & tissue research 200 (1979), S. 443-451 
    ISSN: 1432-0878
    Schlagwort(e): Light scatter sorting ; Thymus ; Cell cycle ; Morphology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Summary Two populations of thymic lymphocytes from eight-week-old mice were separated based on the light scatter intensity they generated while passing through a flow cell analyser. The two populations were subsequently studied morphologically and analysed for the relative amount of DNA present in each cell. Cells having a low light scatter intensity had a high nuclear: cytoplasmic ratio, a heterochromatic nucleus, and a proliferative index (S + G2 + M) of only 23%. Cells with a high light scatter intensity had a low nuclear: cytoplasmic ratio, dispersed chromatin, frequently a uropod with budding microvilli and a proliferative index of 71%. The low light scatter cells resemble small cortical thymocytes or lymphocytes from the thoracic duct described by others. The highest light scatter cells resemble medium lymphocytes shown by others to be proliferative.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 144 (1990), S. 42-51 
    ISSN: 0021-9541
    Schlagwort(e): Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: The shape of the fluidity gradient of the outer hemileaflet of the plasma membrane of normal, living, human white blood cells was determined using a series of n-(9-anthroyloxy) fatty acid probes where n = 2, 3, 6, 7, 9, 11, 12, and 16, to establish a baseline for future studies on the consequences of various pathological states. Fluorescence uptake and steady-state anisotropy values were obtained with a flow cytometer capable of continuous recording over time of vertical and horizontal emission intensities, with the output of these intensities as calculated anisotropy values. The fluorescence uptake of all of the membrane probes was rapid up to about 15 min. The magnitudes of the uptake of fluorescence was, for the n-(9-anthroyioxy) series, in the order 2 〉 3 〉 6 〉 7 〉 9 〉 11 =12 = 16 for neutrophils, lymphocytes, and monocytes. Anisotropy values were constant from 5 to 30 min after addition of the various probes. The orders of the anisotropy magnitudes, indicative of the shapes of the fluidity gradient, were, for neutrophils, 6 〉 7 〉 9 〉 2 = 3 = 11 = 12 〉 16, and for lymphocytes, 7 〉 6 〉 9 〉 11 〉 2 = 3 〉 11 = 12 〉 16, and for monocytes, 9 〉 7 〉 6 〉 11 〉 2 = 3 〉 12 〉 16. The kinetics of anisotropy from 1 to 5 min after addition of the probes differed for each of the three cell types. Probes with an n-value less than or equal to the maxima (n = 6, neutrophils; n = 7, lymphocytes; n = 9, monocytes) rapidly (1.2 min) reached equilibrium, whereas those probes with n-values greater than the maxima took progressively longer times to equilibrate as n increased. This behavior is consistent with the existence of an energy barrier just below the approximate region sensed by the probes, which would correspond to just below 6AS for neutrophils, 7AS for lymphocytes, and 9AS for monocytes.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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