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  • Phloem regeneration  (3)
  • Histochemistry  (2)
  • photochemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 371 (1976), S. 161-170 
    ISSN: 1432-2307
    Keywords: Giant cell granuloma ; Histochemistry ; Ultrastructure ; Cell function ; Osteoclasts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die mehrkernigen Riesenzellen des zentralen Riesenzellgranuloms entstehen durch Zellfusion aus den Pericyten der Kapillaren. In der vorliegenden Studie werden die Funktionsmerkmale der Riesenzellen durch Kombination histologischer, histochemischer und elektronenmikroskopischer Methoden untersucht. In den mehrkernigen Riesenzellen ließen sich in Übereinstimmung mit älteren Untersuchungen die lysosomalen Enzyme saure Phosphatase und Aminopeptidase nachweisen. Das lysosomale System der Riesenzellen befähigt diese zur aktiven Phagocytoseleistung. Darüber hinaus können sich die Riesenzellen neugebildeten Geflechtknochenbälkchen anlagern und osteoclastäre Funktionen übernehmen. Die enzymhistochemische und funktioneile Ähnlichkeit mit den mehrkernigen Osteoclasten wirft die Frage nach einer vergleichbaren Cytogenese beider Zellformen auf.
    Notes: Summary Multinucleated giant cells in giant cell granuloma are formed by cell fusion of capillary pericytes. In our present study we tried to analyze cell function and activity by histologic, histochemical, and electronmicroscopic examination of giant cells. Lysosomal enzymes such as acid phosphatase and amino-peptidase were found in giant cells which is in agreement with former work. By their lysosomal system giant cells are proved phagocytic. In addition, giant cells being localized at trabecular surfaces of newly formed woven bone may develop osteoclastic functions. The enzymatic and functional resemblance of giant cells and multinucleated osteoclasts points to the possibility of a similar cytogenesis of both cell types.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Virchows Archiv 370 (1976), S. 163-175 
    ISSN: 1432-2307
    Keywords: Central giant cell granuloma ; Histogenesis ; Histochemistry ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bisherige Untersuchungen an zentralen Riesenzellgranulomen des Gesichts-Kieferbereiches haben die Histogenese dieser tumorähnlichen Knochenerkrankung nicht klären können. Wir untersuchten daher zwei bioptisch gesicherte zentrale Riesenzellgranulome unter dieser Fragestellung histochemisch und elektronenmikroskopisch. Histochemisch findet sich eine enge Enzymverwandtschaft zwischen den mehrkernigen Riesenzellen und den Pericyten der Kapillaren, die das Granulom dicht durchsetzen. Elektronenmikroskopisch zeigen sich typische Membranphänomene der Zellfusion zwischen den mehrkernigen Riesenzellen und den Pericyten. Die für das Granulom charakteristischen mehrkernigen Riesenzellen entstehen daher durch Zellfusion aus den Pericyten, die als ihre Stammzellen angesehen werden müssen. Da die Pericyten das Granulom auch in Form zahlreicher blinder Kapillarsprossen durchsetzen, erklärt sich die Entwicklung einer Vielzahl von Riesenzellen. Die Ursachen, die diesem Verhalten der Pericyten aetiologisch zugrunde liegen, sind unbekannt. Ob die Cytogenese der Riesenzellen des zentralen Riesenzellgranuloms Modellcharakter hat und analog auch für die Entwicklung von Riesenzellen in anderen Gewebsneubildungen oder für die Enstehung der mehrkernigen Osteoclasten gilt, muß weiteren Untersuchungen vorbehalten bleiben.
    Notes: Summary Until now numerous studies on central giant cell granuloma of jawbones have not been able to reveal the histogenesis of this tumourlike lesion. The aim of the present investigation in two surgically proven cases was to study this question by means of histochemical and electron-microscopic methods. Rather similar histochemieal properties were shown in giant cells and pericytes of capillary sprouts penetrating the granuloma. Cell fusion occurred between both cell types as was observed by electron microscopy. The process of cell fusion is defined by characteristic interdigitations of cell membranes. Therefore pericytes are believed to be the stem cells of multinucleated giant cells in giant cell granuloma. The abundance of giant cells usually occurring in the granuloma might be explained by plenty of capillary sprouts made up by clusters of pericytes. The factors inducing the pericytic cell fusion process are still unknown. The question arises whether cytogenesis of giant cells in giant cell granuloma might be similar in other giant cell lesions or even in the development of multinucleated osteoclasts.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Planta 150 (1980), S. 357-365 
    ISSN: 1432-2048
    Keywords: Cell division pattern ; Coleus ; Phloem regeneration ; Sieve elements, differentiation ; Wound sieve-elements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The wound phloem bridges which have developed six days after interrupting an internodal vascular bundle contain wound sieve-elements, companion cells, and phloem parenchyma cells. An analysis of the meristematic activity responding to the wounding clearly demonstrates that three consecutive divisions are prerequisite to the formation of phloem mother-cells. Companion cells are obligatory sister cells of wound sieve-elements, connected to the latter by specific plasmatic strands and provided with a dense protoplast. Six days after wounding most of the wound sieve-elements are still at a nucleate state of development, but already have characteristic P-protein bodies and plastids containing sieve-element starch. Their cytoplasmic differentiation corresponds to the changes recorded during maturation of ordinary sieve elements. Sieve-plate pores penetrate through preexisting parenchyma cell walls, only, and develop from primary pitfield-plasmodesmata. Wound sieve-elements do not connect to preexisting bundle sieve-elements, they open a new tier of young sieve elements produced by cambial activity.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4994
    Keywords: Fluorescence ; multiplex dyes ; photochemistry ; time-resolved spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract New dyes with characteristic fluorescence lifetimes have been developed for bioanalytical applications. Based upon the concept of “multiplex dyes,” we have designed rhodamine dyes with nearly identical absorption and emission spectral characteristics but different fluorescence lifetimes. Extending this principle to applications with laser diodes, new rhodamines with functional groups for covalent coupling of analytes have been developed. The new labels exhibit absortion and fluorescence beyond 600 nm and have a high quantum efficiency, even in aqueous buffer systems.
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  • 5
    ISSN: 1573-4994
    Keywords: Fluorescence ; photochemistry ; rhodamine dyes ; time-resolved spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The increased sensitivity together with the advent of low-cost optical sources and detectors in the visible-near IR region has led us to current efforts to develop new efficient fluorescent labels for biodiagnostics with absorption and emission beyond 600 nm. In view of the general fluorescence decrease with increasing emission wavelength, we investigated the possibility to shift the absorption of rhodamine dyes toward the region 620–670 nm. The hydrophobic nature of all known long-wavelength dyes results in the tendency to form intra- and intermolecular aggregates in hydrophilic solvents, especially in aqueous environment. Due to the aggregation with biological materials, fluorescence quenching of the dyes is often observed. New strategies for prevention of these processes are considered.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 130 (1986), S. 12-26 
    ISSN: 1615-6102
    Keywords: Phloem initiation ; Phloem regeneration ; Pisum ; Sieve element, sequential differentiation ; Wound-sieve elements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 48 hours after interrupting the root stele ofPisum, wound phloem initiated (proximally or distally to the wound) to reconnect the vascular stumps was found to contain some nucleate wound-sieve elements. At the elongating end of an incomplete wound-sieve tube these elements exhibit a sequence of ultrastructural changes as known from protophloem-sieve tubes. Elongation occurs by the addition of newly divided (wound-) sieve-element/companion-cell complexes. In order to dedifferentiate and assume a new specialization formerly quiescent stelar or cortical cells require at least one (mostly more) preliminary division. Companion cells are consequently obligatory sister cells to wound-sieve elements. By reconstruction using serial sections it could be shown that wound-sieve tubes elongate bidirectionally, starting in an early activated procambial cell of the stele. The elongation is directed by the existence of plasmodesmata, preferably when lying in primary pit fields, and by the plane of preceding divisions. Thus, the developing wound-sieve tube can deviate from the damaged bundle and radiate into the cortex as soon as the plane of the preceding divisions is favourable. In the opposite direction, elongating wound-sieve tubes run parallel to pre-existing phloem traces, thus broading their base at the bundle for the deviating part of the wound-sieve tube. Frequently an individual wound-sieve tube is supplemented at the bundle by a further wound-sieve tube which is partly running parallel to it. Both sieve tubes are interlinked with sieve plates by three-poled sieve elements. Ultrastructurally, the developmental changes of nucleate wound-sieve elements follow the known pattern. In spite of its contrasting origin and odd shape a mature wound-sieve element eventually has the same contents as regular sieve elements: sieve-element plastids, mitochondria, stacked ER and small amounts of P-protein within an electronlucent cytoplasm.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 130 (1986), S. 27-40 
    ISSN: 1615-6102
    Keywords: Phloem contact ; Phloem regeneration ; Pisum ; Sieve pores ; Wound phloem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Following severance of the root stele mature bundle-sieve tubes show a rapid wound response, plugging their sieve pores and depositing callose. Close to the blocked sieve tubes the predetermined but still immature bundle sieve tubes differentiate and consist of mature sieve elements 48 hours after wounding. Within a serially sectioned area the existence of lateral sieve pores connecting blocked bundle-sieve tubes with those which matured after wounding could be proved. Wound-sieve tubes are initiated close to the latter, linked to them by lateral sieve pores. The wound-sieve tubes elongate bidirectionally, parallel to the interrupted phloem trace, until a first (towards the cortex) deviating member is established on one end and, on the other, the length of the common course with the bundle is sufficient for assimilate transfer. Presumably, both initiation and elongation of wound-sieve tubes are guided by preexisting plasmodesmata, which later give rise to sieve pores. Eventually the deviating wound-sieve tubes are in close plasmatic contact with those bundle-sieve tubes which mature after wounding and hence, indirectly, with blocked sieve tubes. One precondition to the restitution of translocation within blocked bundle-sieve tubes is a secondary opening of the plugged sieve pores. The reversibility of callose deposition and the structure of functional pores are discussed. The model of sequential differentiation for channelling auxin in undifferentiated tissue (Sachs 1975) is compared with the sequential differentiation of wound-sieve tubes.
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