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  • 1
    In: European Journal of Immunology, Wiley, Vol. 42, No. 4 ( 2012-04), p. 831-841
    Abstract: T‐cell activation and the subsequent transformation of activated T cells into T ‐cell blasts require profound changes in cell volume. However, the impact of cell volume regulation for T ‐cell immunology has not been characterized. Here we studied the role of the cell‐volume regulating osmolyte transporter T aut for T ‐cell activation in T aut‐deficient mice. T‐cell mediated recall responses were severely impaired in taut −/− mice as shown with B 16 melanoma rejection and hapten‐induced contact hypersensitivity. CD4 + and CD8 + T cells were unequivocally located within peripheral lymph nodes of unprimed taut −/− mice but significantly decreased in taut −/− compared with taut +/+ mice following in vivo activation. Further analysis revealed that T aut is critical for rescuing T cells from activation‐induced cell death in vitro and in vivo as shown with TCR , superantigen, and antigen‐specific activation. Consequently, reduction of CD4 + and CD8 + T cells in taut −/− mice upon antigen challenge resulted in impaired in vivo generation of T ‐cell memory. These findings disclose for the first time that volume regulation in T cells is an element in the regulation of adaptive immune responses and that the osmolyte transporter T aut is crucial for T ‐cell survival and T ‐cell mediated immune reactions.
    Type of Medium: Online Resource
    ISSN: 0014-2980 , 1521-4141
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 1491907-2
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  • 2
    In: The Prostate, Wiley, Vol. 71, No. 10 ( 2011-07), p. 1074-1083
    Abstract: We previously reported that over‐expression of the SEC62 gene is a widespread phenomenon in prostate cancer. Since the use of endoplasmic reticulum (ER) stress‐inducing substances such as thapsigargin in prostate cancer therapy is widely discussed in the literature, we investigated the influence of Sec62 protein content on the cellular response to these drugs. METHODS Growth effects were analyzed by real‐time cell analysis and viability tests in DU145‐cells representing an increased SEC62 expression or PC3‐ and LNCaP‐cells representing a similar SEC62 expression compared to non‐tumor cells. Ca 2+ ‐imaging in an established HeLa‐system with fluorescent dye was used to study molecular effects of Sec62 depletion. RESULTS We found a lower propensity toward apoptotic cell death after thapsigargin treatment for DU145 cells compared to PC3 or LNCaP and siRNA‐mediated silencing of SEC62 resulted in a reduced viability of thapsigargin‐treated PC3 cells, indicating that Sec62 functions in cellular stress response. Measurement of cytosolic [Ca 2+ ] demonstrated the influence of Sec62 on the cellular response to thapsigargin on a molecular level. Using real‐time cell analysis, we observed the loss of androgen stimulation of LNCaP cells in the presence of thapsigargin, and an additional negative effect on cell growth of Sec62 depletion. Also, for PC3‐ and DU145‐cells Sec62 depletion inhibited growth after thapsigargin treatment. CONCLUSIONS Our data indicate a crucial function of Sec62 in the response to thapsigargin‐induced ER stress. This will be of great significance on the background of elevated Sec62 protein levels in prostate cancer cells when treatment with thapsigargin analogs is considered. Prostate 71:1074–1083, 2011. © 2011 Wiley‐Liss, Inc.
    Type of Medium: Online Resource
    ISSN: 0270-4137 , 1097-0045
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 1494709-2
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  • 3
    Online Resource
    Online Resource
    Wiley ; 2014
    In:  Oikos Vol. 123, No. 10 ( 2014-10), p. 1224-1233
    In: Oikos, Wiley, Vol. 123, No. 10 ( 2014-10), p. 1224-1233
    Abstract: Soil systems maintain important ecosystem processes crucial for plant life and food production. Especially agricultural systems are strongly affected by climate change due to low vegetation cover associated with high temperatures and drought. Nevertheless, the response of soil systems to climate change is little explored. We used microcosms with a simplified soil community to address effects of climate change using independent temperature and dryness gradients and addressed their effects on top–down control and litter decomposition. The community consisted of maize litter as a basal resource, fungi, springtails and as top predators mites and centipedes. As the body‐size structure is of high importance for communities, we included differently‐sized springtails and predator species. After seven weeks, the experiment was terminated, and the impact of climate change on direct feeding interactions and indirect effects across trophic levels was analysed. With increasing temperature and dryness, consumption rates increased, thereby amplifying the negative influence of consumer populations on their resources. Hence, these climate‐change variables increased the top–down control of 1) predators (mainly mites) on springtails and 2) fungi on litter decomposition. In addition, we found that the climate‐change variables strengthened trophic cascades from predators on fungi whose density was thus increasingly decoupled from top–down control by their springtail consumers. Their increased decomposition rates are of high importance for carbon cycling and may result in accelerated nutrient turnover. In conclusion, our results suggest that climate change may strongly influence the structure and functioning of soil systems by strengthening consumption rates and trophic cascades, which will have far reaching consequences for the nutrient turnover and productivity of agricultural ecosystems.
    Type of Medium: Online Resource
    ISSN: 0030-1299 , 1600-0706
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2025658-9
    detail.hit.zdb_id: 207359-6
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Wiley ; 2012
    In:  Journal of Animal Ecology Vol. 81, No. 3 ( 2012-05), p. 516-523
    In: Journal of Animal Ecology, Wiley, Vol. 81, No. 3 ( 2012-05), p. 516-523
    Abstract: 1.  Model analyses show that the stability of population dynamics and food web persistence increase with the strength of interference competition. Despite this critical importance for community stability, little is known about how external factors such as the environmental temperature affect intraspecific interference competition. 2.  We aimed to fill this void by studying the functional responses of two ground beetle species of different body size, Pterostichus melanarius and Poecilus versicolor . These functional response experiments were replicated across four predator densities and two temperatures to address the impact of temperature on intraspecific interference competition. 3.  We generally expected that warming should increase the speed of movement, encounter rates and in consequence interference among predator individuals. In our experiment, this expectation was supported by the results obtained for the larger predator, P. melanarius , whereas the opposite pattern characterized the interference behaviour of the smaller predator P. versicolor. 4.  These results suggest potentially nontrivial implications for the effects of environmental temperature on intraspecific interference competition, for which we propose an explanation based on the different sensitivity to warming of metabolic rates of both species. As expected, increasing temperature led to stronger interference competition of the larger species, P. melanarius , which exhibited a weaker increase in metabolic rate with increasing temperature. The stronger increase in the metabolic rate of the smaller predator, P. versicolor , had to be compensated by increasing searching activity for prey, which did not leave time for increasing interference. 5.  Together, these results suggest that any generalization how interference competition responds to warming should also take the species’ metabolic response to temperature increases into account.
    Type of Medium: Online Resource
    ISSN: 0021-8790 , 1365-2656
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 2006616-8
    SSG: 12
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  • 5
    In: Journal of Plant Nutrition and Soil Science, Wiley, Vol. 173, No. 5 ( 2010-10), p. 644-653
    Type of Medium: Online Resource
    ISSN: 1436-8730 , 1522-2624
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2010
    detail.hit.zdb_id: 1481142-X
    detail.hit.zdb_id: 1470765-2
    detail.hit.zdb_id: 200063-5
    SSG: 12
    SSG: 13
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  • 6
    In: Clinical Endocrinology, Wiley, Vol. 80, No. 1 ( 2014-01), p. 65-72
    Abstract: Chemerin is a novel adipokine implicated in inflammation and obesity. We hypothesized that foetal chemerin would be elevated in gestational diabetes mellitus ( GDM ) and correlate with foetal and maternal adiposity. Design Observational, longitudinal study. Subjects and measurements Foetal chemerin was measured separately in arterial and venous cord blood of 30 infants born to mothers with ( n  = 15) and without GDM ( n  = 15), in their mothers in early third trimester and at delivery and in amniotic fluid (week 32) of women with GDM . Expression of chemerin and its receptor in human foetal tissues commercially available and in placental cells was measured by quantitative PCR . Associations between foetal and maternal anthropometric and metabolic variables were assessed in multivariate regression models. Results In GDM, foetal arterial but not venous cord blood chemerin levels were elevated by about 60% ( P   〈  0·05). Venous cord blood chemerin was higher in infants of obese women ( P   〈  0·01). In multivariate analyses, neither amniotic fluid nor cord blood chemerin levels correlated with birth weight or ponderal index. Both arterial and venous chemerin levels were related to maternal chemerin at birth, and arterial chemerin was associated with GDM status in addition. Maternal levels were unaltered in GDM, but higher in maternal obesity. Foetal liver produces fourfold more chemerin mRNA than other foetal tissues, whereas its receptor prevails in spleen. Conclusions Based on multivariate analyses, foetal growth appears unrelated to foetal chemerin. Maternal obesity and GDM have differential effects on foetal chemerin levels. Site of major production (liver) and action (spleen) differ in human foetal tissues.
    Type of Medium: Online Resource
    ISSN: 0300-0664 , 1365-2265
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2004597-9
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