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741.
742.
Capacity for NADPH regeneration in the leaves of two poplar genotypes differing in ozone sensitivity
Ata Allah Dghim Jennifer Dumont Marie‐Paule Hasenfratz‐Sauder Pierre Dizengremel Didier Le Thiec Yves Jolivet 《Physiologia plantarum》2013,148(1):36-50
Cell capacity for cytosolic NADPH regeneration by NADP‐dehydrogenases was investigated in the leaves of two hybrid poplar (Populus deltoides × Populus nigra) genotypes in response to ozone (O3) treatment (120 ppb for 17 days). Two genotypes with differential O3 sensitivity were selected, based on visual symptoms and fallen leaves: Robusta (sensitive) and Carpaccio (tolerant). The estimated O3 flux (POD0), that entered the leaves, was similar for the two genotypes throughout the treatment. In response to that foliar O3 flux, CO2 assimilation was inhibited to the same extent for the two genotypes, which could be explained by a decrease in Rubisco (EC 4.1.1.39) activity. Conversely, an increase in PEPC (EC 4.1.1.31) activity was observed, together with the activation of certain cytosolic NADP‐dehydrogenases above their constitutive level, i.e. NADP‐G6PDH (EC 1.1.1.49), NADP‐ME (malic enzyme) (EC 1.1.1.40) and NADP‐ICDH (NADP‐isocitrate dehydrogenase) (EC1.1.1.42). However, the activity of non‐phosphorylating NADP‐GAPDH (EC 1.2.1.9) remained unchanged. From the 11th fumigation day, NADP‐G6PDH and NADP‐ME profiles made it possible to differentiate between the two genotypes, with a higher activity in Carpaccio than in Robusta. At the same time, Carpaccio was able to maintain high levels of NADPH in the cells, while NADPH levels decreased in Robusta O3‐treated leaves. All these results support the hypothesis that the capacity for cells to regenerate the reducing power, especially the cytosolic NADPH pool, contributes to improve tolerance to high ozone exposure. 相似文献
743.
Maxime Séleck Jean-Philippe Bizoux Gilles Colinet Michel-Pierre Faucon Arielle Guillaume Pierre Meerts Julien Piqueray Grégory Mahy 《Plant and Soil》2013,373(1-2):455-469
Aims
Define the chemical factors structuring plant communities of three copper-cobalt outcrops (Tenke-Fungurume, Katangan Copperbelt, D. R. Congo) presenting extreme gradients.Methods
To discriminate plant communities, 172 vegetation records of all species percentage cover were classified based on NMDS and the Calinski criterion. Soil samples were analyzed for 13 chemical factors and means compared among communities with ANOVA. Partial canonical correspondence analysis (pCCA) was used to determine amount of variation explained individually by each factor and site effect.Results
Seven communities were identified. Six of the studied communities were related to distinct sites. Site effect (6.0 % of global inertia) was identified as the most important factor related to plant communities’ variation followed by Cu (5.5 %), pH (3.6 %) and Co (3.5 %). Unique contribution of site effect (3.8 %) was higher than that of Cu (1.1 %) and Co (1.0 %).Conclusions
In restoration, not only Cu and Co contents will be important to maintain vegetation diversity, attention should also be given to co-varying factors potentially limiting toxicity of metals: pH, organic matter, Ca and Mn. Physical parameters were also identified as important in the creation of adequate conditions for diverse communities. Further studies should focus on the effect of physical parameters and geology. 相似文献744.
745.
746.
Pierre L. van den Berghe Walker Connor A. H. M. Kirk‐Greene Robert Mahuta Robert Miles John Beattie 《Ethnic and racial studies》2013,36(4):484-498
Milton M. Gordon, HUMAN NATURE, CLASS AND ETHNICITY. London and New York, Oxford University Press, 1978, 302 pp., £6.50, $11.95 ($3.50 paper). June Teufel Dreyer, CHINA'S FORTY MILLIONS: MINORITY NATIONALITIES AND NATIONAL INTEGRATION IN THE PEOPLE'S REPUBLIC OF CHINA. Cambridge (Mass.) and London, Harvard University Press, 1976, 333 pp., £9.55. W. Stanford Reid (ed), THE SCOTTISH TRADITION IN CANADA. Toronto, McClelland & Stewart, 1976, xi + 324 pp., $12.55. I. H. Kawharu, MAORI LAND TENURE: STUDIES OF A CHANGING INSTITUTION. Oxford, Clarendon Press, 1977, 362 pp., £13.50. David T. Wellman, PORTRAITS OF WHITE RACISM. London, Cambridge University Press, 1977, 254 pp., £9.50 (£4.00 paper). Lucy Mair, AFRICAN KINGDOMS. Oxford, Clarendon Press, 1977, 151 pp., £3.95, (£1.95 paper). Roger Scott, NORTHERN IRELAND: THE POLITICS OF VIOLENCE. Canberra Series in Administrative Studies 2., Canberra College of Advanced Education, 1977, 84 pp., n.p. James A. Geschwender, CLASS, RACE AND WORKER INSURGENCY: THE LEAGUE OF BLACK REVOLUTIONARY WORKERS. London, Cambridge University Press, 1977, 249 pp., £8.50 (£3.50 paper). Crawford Young, THE POLITICS OF CULTURAL PLURALISM. Madison, University of Wisconsin Press, 1976. 560 pp., £13.60. D. C. R. A. Goonetilleke, DEVELOPING COUNTRIES IN BRITISH FICTION. London, Macmillan, 1977, 282 pp., £8.95. M. M. Mahood, THE COLONIAL ENCOUNTER. London, Rex Collings, 1977, 210 pp., £4.75. Brian V. Street, THE SAVAGE IN LITERATURE. London, Routledge & Kegan Paul, 1975, 207 pp., £5.75. 相似文献
747.
748.
Émilie Degagné Jade Degrandmaison Djordje M. Grbic Valérie Vinette Guillaume Arguin Fernand‐Pierre Gendron 《Journal of cellular physiology》2013,228(1):99-109
P2Y2 receptor expression is increased in intestinal epithelial cells (IECs) during inflammatory bowel diseases (IBDs). In this context, P2Y2 stimulates PGE2 release by IECs, suggesting a role in wound healing. For this study, we have used the non‐cancerous IEC‐6 cell line. IEC‐6 cell migration was determined using Boyden chambers and the single‐edged razor blade model of wounding. The receptor was activated using ATP, UTP, or 2‐thioUTP. Pharmacological inhibitors, a blocking peptide, a neutralizing antibody and interfering RNAs were used to characterize the signaling events. Focal adhesions and microtubule (MT) dynamics were determined by immunofluorescence using anti‐vinculin and anti‐acetylated‐α‐tubulin antibodies, respectively. In vivo, the dextran sodium sulfate mouse model of colitis was used to characterize the effects of P2Y2 agonist 2‐thioUTP on remission. We showed that P2Y2 increased cell migration and wound closure by recruiting Go protein with the cooperation of integrin αv. Following P2Y2 activation, we demonstrated that GSK3β activity was inhibited in response to Akt activation. This leads to MT stabilization and increased number of focal adhesions. In vivo, P2Y2 activation stimulates remission, as illustrated by a reduction in the disease activity index values and histological scores as compared to control mice. These findings highlight a novel function for this receptor in IECs. They also illustrate that P2Y receptors could be targeted for the development of innovative therapies for the treatment of IBDs. J. Cell. Physiol. 228: 99–109, 2013. © 2012 Wiley Periodicals, Inc. 相似文献
749.
Jean‐François Bourzac Karine L'Ériger Jean‐François Larrivée Guillaume Arguin Maude S. Bilodeau Jana Stankova Fernand‐Pierre Gendron 《Journal of cellular physiology》2013,228(1):120-129
With the diabetes epidemic affecting the world population, there is an increasing demand for means to regulate glycemia. Dietary glucose is first absorbed by the intestine before entering the blood stream. Thus, the regulation of glucose absorption by intestinal epithelial cells (IECs) could represent a way to regulate glycemia. Among the molecules involved in glycemia homeostasis, extracellular ATP, a paracrine signaling molecule, was reported to induce insulin secretion from pancreatic β cells by activating P2Y and P2X receptors. In rat's jejunum, P2X7 expression was previously immunolocalized to the apex of villi, where it has been suspected to play a role in apoptosis. However, using an antibody recognizing the receptor extracellular domain and thus most of the P2X7 isoforms, we showed that expression of this receptor is apparent in the top two‐thirds of villi. These data suggest a different role for this receptor in IECs. Using the non‐cancerous IEC‐6 cells and differentiated Caco‐2 cells, glucose transport was reduced by more than 30% following P2X7 stimulation. This effect on glucose transport was not due to P2X7‐induced cell apoptosis, but rather was the consequence of glucose transporter 2 (Glut2)'s internalization. The signaling pathway leading to P2X7‐dependent Glut2 internalization involved the calcium‐independent activation of phospholipase Cγ1 (PLCγ1), PKCδ, and PKD1. Although the complete mechanism regulating Glut2 internalization following P2X7 activation is not fully understood, modulation of P2X7 receptor activation could represent an interesting approach to regulate intestinal glucose absorption. J. Cell. Physiol. 228: 120–129, 2013. © 2012 Wiley Periodicals, Inc. 相似文献
750.
Simon Ladevèze Laurence Tarquis Davide A. Cecchini Juliette Bercovici Isabelle André Christopher M. Topham Sandrine Morel Elisabeth Laville Pierre Monsan Vincent Lombard Bernard Henrissat Gabrielle Potocki-Véronèse 《The Journal of biological chemistry》2013,288(45):32370-32383
To metabolize both dietary fiber constituent carbohydrates and host glycans lining the intestinal epithelium, gut bacteria produce a wide range of carbohydrate-active enzymes, of which glycoside hydrolases are the main components. In this study, we describe the ability of phosphorylases to participate in the breakdown of human N-glycans, from an analysis of the substrate specificity of UhgbMP, a mannoside phosphorylase of the GH130 protein family discovered by functional metagenomics. UhgbMP is found to phosphorolyze β-d-Manp-1,4-β-d-GlcpNAc-1,4-d-GlcpNAc and is also a highly efficient enzyme to catalyze the synthesis of this precious N-glycan core oligosaccharide by reverse phosphorolysis. Analysis of sequence conservation within family GH130, mapped on a three-dimensional model of UhgbMP and supported by site-directed mutagenesis results, revealed two GH130 subfamilies and allowed the identification of key residues responsible for catalysis and substrate specificity. The analysis of the genomic context of 65 known GH130 sequences belonging to human gut bacteria indicates that the enzymes of the GH130_1 subfamily would be involved in mannan catabolism, whereas the enzymes belonging to the GH130_2 subfamily would rather work in synergy with glycoside hydrolases of the GH92 and GH18 families in the breakdown of N-glycans. The use of GH130 inhibitors as therapeutic agents or functional foods could thus be considered as an innovative strategy to inhibit N-glycan degradation, with the ultimate goal of protecting, or restoring, the epithelial barrier. 相似文献