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21.
Arabidopsis mutants define a central role for the xanthophyll cycle in the regulation of photosynthetic energy conversion. 总被引:9,自引:1,他引:8
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A conserved regulatory mechanism protects plants against the potentially damaging effects of excessive light. Nearly all photosynthetic eukaryotes are able to dissipate excess absorbed light energy in a process that involves xanthophyll pigments. To dissect the role of xanthophylls in photoprotective energy dissipation in vivo, we isolated Arabidopsis xanthophyll cycle mutants by screening for altered nonphotochemical quenching of chlorophyll fluorescence. The npq1 mutants are unable to convert violaxanthin to zeaxanthin in excessive light, whereas the npq2 mutants accumulate zeaxanthin constitutively. The npq2 mutants are new alleles of aba1, the zeaxanthin epoxidase gene. The high levels of zeaxanthin in npq2 affected the kinetics of induction and relaxation but not the extent of nonphotochemical quenching. Genetic mapping, DNA sequencing, and complementation of npq1 demonstrated that this mutation affects the structural gene encoding violaxanthin deepoxidase. The npq1 mutant exhibited greatly reduced nonphotochemical quenching, demonstrating that violaxanthin deepoxidation is required for the bulk of rapidly reversible nonphotochemical quenching in Arabidopsis. Altered regulation of photosynthetic energy conversion in npq1 was associated with increased sensitivity to photoinhibition. These results, in conjunction with the analysis of npq mutants of Chlamydomonas, suggest that the role of the xanthophyll cycle in nonphotochemical quenching has been conserved, although different photosynthetic eukaryotes rely on the xanthophyll cycle to different extents for the dissipation of excess absorbed light energy. 相似文献
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C-peptide has intrinsic biological activity and may be renoprotective. We conducted a systematic review to determine whether C-peptide had a beneficial effect on renal outcomes. MEDLINE, EMBASE, and the Cochrane Central Databases were searched for human and animal studies in which C-peptide was administered and renal endpoints were subsequently measured. We identified 4 human trials involving 74 patients as well as 18 animal studies involving 35 separate experiments with a total of 641 animals. In humans, the renal effects of exogenously delivered C-peptide were only studied in type 1 diabetics with either normal renal function or incipient nephropathy. Pooled analysis showed no difference in GFR (mean difference, -1.36 mL/min/1.73 m2, p = 0.72) in patients receiving C-peptide compared to a control group, but two studies reported a reduction in glomerular hyperfiltration (p<0.05). Reduction in albuminuria was also reported in the C-peptide group (p<0.05). In diabetic rodent models, C-peptide led to a reduction in GFR (mean difference, -0.62 mL/min, p<0.00001) reflecting a partial reduction in glomerular hyperfiltration. C-peptide also reduced proteinuria (mean difference, -186.25 mg/day, p = 0.05), glomerular volume (p<0.00001), and mesangial matrix area (p<0.00001) in diabetic animals without affecting blood pressure or plasma glucose. Most studies were relatively short-term in duration, ranging from 1 hour to 3 months. Human studies of sufficient sample size and duration are needed to determine if the beneficial effects of C-peptide seen in animal models translate into improved long-term clinical outcomes for patients with chronic kidney disease. (PROSPERO CRD42014007472) 相似文献
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Bo Chen Allison L. Miller Marlon Rebelatto Yambasu Brewah Daniel C. Rowe Lori Clarke Meggan Czapiga Kim Rosenthal Tomozumi Imamichi Yan Chen Chew-Shun Chang Partha S. Chowdhury Brian Naiman Yue Wang De Yang Alison A. Humbles Ronald Herbst Gary P. Sims 《PloS one》2015,10(2)
Release of endogenous damage associated molecular patterns (DAMPs), including members of the S100 family, are associated with infection, cellular stress, tissue damage and cancer. The extracellular functions of this family of calcium binding proteins, particularly S100A8, S100A9 and S100A12, are being delineated. They appear to mediate their functions via receptor for advanced glycation endproducts (RAGE) or TLR4, but there remains considerable uncertainty over the relative physiological roles of these DAMPs and their pattern recognition receptors. In this study, we surveyed the capacity of S100 proteins to induce proinflammatory cytokines and cell migration, and the contribution RAGE and TLR4 to mediate these responses in vitro. Using adenoviral delivery of murine S100A9, we also examined the potential for S100A9 homodimers to trigger lung inflammation in vivo. S100A8, S100A9 and S100A12, but not the S100A8/A9 heterodimer, induced modest levels of TLR4-mediated cytokine production from human PBMC. In contrast, for most S100s including S100A9, RAGE blockade inhibited S100-mediated cell migration of THP1 cells and major leukocyte populations, whereas TLR4-blockade had no effect. Intranasal administration of murine S100A9 adenovirus induced a specific, time-dependent predominately macrophage infiltration that coincided with elevated S100A9 levels and proinflammatory cytokines in the BAL fluid. Inflammatory cytokines were markedly ablated in the TLR4-defective mice, but unexpectedly the loss of TLR4 signaling or RAGE-deficiency did not appreciably impact the S100A9-mediated lung pathology or the inflammatory cell infiltrate in the alveolar space. These data demonstrate that physiological levels of S100A9 homodimers can trigger an inflammatory response in vivo, and despite the capacity of RAGE and TLR4 blockade to inhibit responses in vitro, the response is predominately independent of both these receptors. 相似文献
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Aimee M. Terauchi Graham Peers Marilyn C. Kobayashi Krishna K. Niyogi Sabeeha S. Merchant 《Photosynthesis research》2010,105(1):39-49
To investigate the impact of iron deficiency on bioenergetic pathways in Chlamydomonas, we compared growth rates, iron content,
and photosynthetic parameters systematically in acetate versus CO2-grown cells. Acetate-grown cells have, predictably (2-fold) greater abundance of respiration components but also, counter-intuitively,
more chlorophyll on a per cell basis. We found that phototrophic cells are less impacted by iron deficiency and this correlates
with their higher iron content on a per cell basis, suggesting a greater capacity/ability for iron assimilation in this metabolic
state. Phototrophic cells maintain both photosynthetic and respiratory function and their associated Fe-containing proteins
in conditions where heterotrophic cells lose photosynthetic capacity and have reduced oxygen evolution activity. Maintenance
of NPQ capacity might contribute to protection of the photosynthetic apparatus in iron-limited phototrophic cells. Acetate-grown
iron-limited cells maintain high growth rates by suppressing photosynthesis but increasing instead respiration. These cells
are also able to maintain a reduced plastoquinone pool. 相似文献
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Arthur R. Grossman Steven J. Karpowicz Mark Heinnickel David Dewez Blaise Hamel Rachel Dent Krishna K. Niyogi Xenie Johnson Jean Alric Francis-André Wollman Huiying Li Sabeeha S. Merchant 《Photosynthesis research》2010,106(1-2):3-17
Chlamydomonas reinhardtii, a unicellular green alga, has been exploited as a reference organism for identifying proteins and activities associated with the photosynthetic apparatus and the functioning of chloroplasts. Recently, the full genome sequence of Chlamydomonas was generated and a set of gene models, representing all genes on the genome, was developed. Using these gene models, and gene models developed for the genomes of other organisms, a phylogenomic, comparative analysis was performed to identify proteins encoded on the Chlamydomonas genome which were likely involved in chloroplast functions (or specifically associated with the green algal lineage); this set of proteins has been designated the GreenCut. Further analyses of those GreenCut proteins with uncharacterized functions and the generation of mutant strains aberrant for these proteins are beginning to unmask new layers of functionality/regulation that are integrated into the workings of the photosynthetic apparatus. 相似文献
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Shovonlal Roy Sabyasachi Bhattacharya Partha Das Joydev Chattopadhyay 《Journal of biological physics》2007,33(1):1-17
We explore the mutual dependencies and interactions among different groups of species of the plankton population, based on
an analysis of the long-term field observations carried out by our group in the North–West coast of the Bay of Bengal. The
plankton community is structured into three groups of species, namely, non-toxic phytoplankton (NTP), toxic phytoplankton
(TPP) and zooplankton. To find the pair-wise dependencies among the three groups of plankton, Pearson and partial correlation
coefficients are calculated. To explore the simultaneous interaction among all the three groups, a time series analysis is
performed. Following an Expectation Maximization (E-M) algorithm, those data points which are missing due to irregularities
in sampling are estimated, and with the completed data set a Vector Auto-Regressive (VAR) model is analyzed. The overall analysis
demonstrates that toxin-producing phytoplankton play two distinct roles: the inhibition on consumption of toxic substances
reduces the abundance of zooplankton, and the toxic materials released by TPP significantly compensate for the competitive
disadvantages among phytoplankton species. Our study suggests that the presence of TPP might be a possible cause for the generation
of a complex interaction among the large number of phytoplankton and zooplankton species that might be responsible for the
prolonged coexistence of the plankton species in a fluctuating biomass. 相似文献
30.
Biswas PS Pedicord V Ploss A Menet E Leiner I Pamer EG 《Journal of immunology (Baltimore, Md. : 1950)》2007,179(7):4520-4528
Regulation of CD8 T cell expansion and contraction is essential for successful immune defense against intracellular pathogens. IL-10 is a regulatory cytokine that can restrict T cell responses by inhibiting APC functions. IL-10, however, can also have direct effects on T cells. Although blockade or genetic deletion of IL-10 enhances T cell-mediated resistance to infections, the extent to which IL-10 limits in vivo APC function or T cell activation/proliferation remains unknown. Herein, we demonstrate that primary and memory CD8 T cell responses following Listeria monocytogenes infection are enhanced by the absence of IL-10. Surface expression of the IL-10R is transiently up-regulated on CD8 T cells following activation, suggesting that activated T cells can respond to IL-10 directly. Consistent with this notion, CD8 T cells lacking IL-10R2 underwent greater expansion than wild-type T cells upon L. monocytogenes infection. The absence of IL-10R2 on APCs, in contrast, did not enhance T cell responses following infection. Our studies demonstrate that IL-10 produced during bacterial infection directly limits expansion of pathogen-specific CD8 T cells and reveal an extrinsic regulatory mechanism that modulates the magnitude of memory T cell responses. 相似文献