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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cytotechnology 12 (1993), S. 325-345 
    ISSN: 1573-0778
    Keywords: cell cycle arrest ; cell membrane ; DNA repair ; oncogene ; radiation resistance ; signal transduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Cells and tissues have developed a variety of ways of responding to a hostile environment, be it from drugs (toxins) or radiation (summarized in Fig. 1). Three categories of radiation damage limitation are: (i) DNA repair (ii) changes in cellular metabolism (iii) changes in cell interaction (cell contact or tissue-based resistance; whole organism based resistance). DNA repair has been evaluated predominantly by the study of repair-deficient mutants. The function of the repair genes they lack is not fully understood, but some of their important interactions are now characterized. For example, the interaction of transcription factors with nucleotide excision repair is made clear by the genetic syndromes of xeroderma-pigmentosum groups B, D and G. These diseases demonstrate ultraviolet light sensitivity and general impairment of transcription: they are linked by impaired unwinding of the DNA required for both transcription and repair. The transfer of DNA into cells is sometimes accompanied by a change in sensitivity to radiation, and this is of special interest when this is the same genetic change seen in tumors. DNA repair has a close relationship with the cell cycle and cell cycle arrest in response to damage may determine sensitivity to that damage. DNA repair mechanisms in response to a variety of drugs and types of radiation can be difficult to study because of the inability to target the damage to defined sequencesin vivo and the lack of a statisfactory substrate forin vitro studies. Changes in cellular metabolism as a result of ionizing radiation can impart radiation resistance, which is usually transientin vitro, but may be more significantin vivo for tissues or tumors. The mechanisms by which damage is sensed by cells is unknown. The detection of free radicals is thought likely, but distortion to DNA structure or strand breakage and a direct effect on membranes are other possibilities for which there is evidence. Changes in extracellular ATP occur in response to damage, and this could be a direct membrane effect. External purinergic receptors can then be involved in signal transduction pathways resulting in altered levels of thiol protection or triggering apoptosis. Changes in the functional level of proteins as a consequence of ionizing radiation include transcription factors, for example c-jun and c-fos; cell cycle arrest proteins such as GADD (growth arrest and DNA damage inducible proteins) and p53; growth factors such as FGF, PDGF; and other proteins leading to radioresistance. Mechanisms for intercellular resistance could be mediated by cell contact, such as gap junctions, which may help resistance to radiation in non-cycling cells. Paracrine response mechanisms, such as the release of angiogenic factors via membrane transport channels may account for tissue and tumor radiation resistance. Endocrine response mechanisms may also contribute to tissue or tumor resistance.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 559-563 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The products of the reaction between fullerenes (C60/C70) and dimethylamine were investigated by fast atom bombardment (FAB) mass spectrometry and tandem mass spectrometry (MS/MS). The FAB mass spectrum shows peaks corresponding to the addition of up to eight dimethylamine species, exclusively to C70. MS/MS reveals an unusual fragmentation pattern. The mass spectrum of the reaction products, together with a number of tandem mass spectra, are shown.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 22 (1993), S. 712-720 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bacitracin is a mixture of polypeptide antibiotics produced by the action of Bacillus subtilis and Bacillus licheniformis. The mixture has previously been shown to contain at least ten components, of which only the major component, Bacitracin A, and its oxidized counterpart, Bacitracin F, have been fully structurally evaluated. Using fast atom bombardment ionization with tandem mass spectrometry, three isobaric components of one of the minor constituents of the mixture, Bacitracin B, have been structurally characterized, delineating the three single substitution sites within Bactitracin A where Ile has been replaced by Val.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2022-05-25
    Description: Author Posting. © Society for Neuroscience, 2005. This article is posted here by permission of Society for Neuroscience for personal use, not for redistribution. The definitive version was published in Journal of Neuroscience 25 (2005): 2853-2864, doi:10.1523/JNEUROSCI.4313-04.2005.
    Description: Ca2+ signals in neurons use specific temporal and spatial patterns to encode unambiguous information about crucial cellular functions. To understand the molecular basis for initiation and propagation of inositol 1,4,5-trisphosphate (InsP3)-mediated intracellular Ca2+ signals, we correlated the subcellular distribution of components of the InsP3 pathway with measurements of agonist-induced intracellular Ca2+ transients in cultured rat hippocampal neurons and pheochromocytoma cells. We found specialized domains with high levels of phosphatidylinositol-4-phosphate kinase (PIPKIγ) and chromogranin B (CGB), proteins acting synergistically to increase InsP3 receptor (InsP3R) activity and sensitivity. In contrast, Ca2+ pumps in the plasma membrane (PMCA) and sarco-endoplasmic reticulum as well as buffers that antagonize the rise in intracellular Ca2+ were distributed uniformly. By pharmacologically blocking phosphatidylinositol-4-kinase and PIPKIγ or disrupting the CGB-InsP3R interaction by transfecting an interfering polypeptide fragment, we produced major changes in the initiation site and kinetics of the Ca2+ signal. This study shows that a limited number of proteins can reassemble to form unique, spatially restricted signaling domains to generate distinctive signals in different regions of the same neuron. The finding that the subcellular location of initiation sites and protein microdomains was cell type specific will help to establish differences in spatiotemporal Ca2+ signaling in different types of neurons.
    Description: This work was supported by grants from the National Institutes of Health (GM63496, DK61747 to B.E.E., and MH67830 to M.F.Y.), Whitehall Foundation (M.F.Y.), German National Merit Foundation (S.N.J. and C.-U.C.), and Vetenskapsrådet, the Swedish Research Council (P.U.).
    Keywords: InsP3 ; PIPKIγ ; Chromogranin ; Signaling microdomain ; Calcium imaging ; Hippocampal neurons
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 5
    Publication Date: 2011-08-16
    Description: Beta Cephei star discovery criteria, examining mu-mechanism theory by He and N overabundances, far UV flux, spectral line width and binary character
    Keywords: SPACE SCIENCES
    Type: ; TROPHYSICAL JOURNAL
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  • 6
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    In:  Other Sources
    Publication Date: 2011-08-16
    Description: Polytropic models second order pulsations, evaluating stellar pulsational stability and thermal imbalance
    Keywords: SPACE SCIENCES
    Type: ; BROTECHNIKA, NO. 1(
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  • 7
    Publication Date: 2011-08-16
    Description: Massive homogeneous star pulsation stability, determining maximum mass by opacity formula
    Keywords: SPACE SCIENCES
    Type: ; 37 (
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  • 8
    Publication Date: 2011-08-12
    Description: Nuclear energized pulsational instability of stars based on linear quasi-adiabatic theory, including models with hydrogen burning shells
    Keywords: SPACE SCIENCES
    Type: ; ADEMIE DES SCIENCES
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  • 9
    Publication Date: 2011-08-12
    Description: Structure and pulsational properties of massive stars with helium cores and thin hydrogen poor envelopes
    Keywords: SPACE SCIENCES
    Type: ; 565 (
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  • 10
    Publication Date: 2011-08-12
    Description: Variable stars blue sequence, proposing mu mechanism and beta mechanism as explanation for radial pulsations
    Keywords: SPACE SCIENCES
    Type: ; TROPHYSICAL JOURNAL
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