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Seasonal dymanic of the infestation of young landlocked salmon (Salmo salar morpha sebago, Girard) by the monogenean species Gyrodactylus salaris Malberg, 1957 was studied in the river Lizhma, Karelia. It is established, that the temperature optimal for the development and reproduction of the parasite is about 3-8 degrees C. It is stated, that the abundance of G. salaris in the river Lizhma do not reach so high values, as it was observed in the regions outside the natural area of the parasite. 相似文献
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Using circulant symmetry to model featureless objects 总被引:1,自引:0,他引:1
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Youjin Lee Jieun Jung Kyung Jin Cho Seoung‐Kwan Lee Jong‐Wan Park IL‐Hoan Oh Gi Jin Kim 《Journal of cellular biochemistry》2013,114(1):79-88
Hypoxia triggers physiological and pathological cellular processes, including proliferation, differentiation, and death, in several cell types. Mesenchymal stem cells (MSCs) derived from various tissues have self‐renewal activity and can differentiate towards multiple lineages. Recently, it has been reported that hypoxic conditions tip the balance between survival and death by hypoxia‐induced autophagy, although the underlying mechanism is not clear. The objectives of this study are to compare the effect of hypoxia on the self‐renewal of bone marrow‐derived mesenchymal stem cells (BM‐MSCs) and placental chorionic plate‐derived mesenchymal stem cells (CP‐MSCs) and to investigate the regulatory mechanisms of self‐renewal in each MSC type during hypoxia. The expression of self‐renewal markers (e.g., Oct4, Nanog, Sox2) was assessed in both cell lines. PI3K and stem cell factor (SCF) expression gradually increased in CP‐MSCs but were markedly downregulated in BM‐MSCs by hypoxia. The phosphorylation of ERK and mTOR was augmented by hypoxia in CP‐MSCs compared to control. Also, the expression of LC3 II, a component of the autophagosome and the hoof‐shaped autophagosome was detected more rapidly in CP‐MSCs than in BM‐MSCs under hypoxia. Hypoxia induced the expression of SCF in CP‐MSCs and increased SCF/c‐kit pathway promotes the self‐renewal activities of CP‐MSCs via an autocrine/paracrine mechanism that balances cell survival and cell death events by autophagy. These activities occur to a greater extent in CP‐MSCs than in BM‐MSCs through regulating the phosphorylation of mTOR. These findings will provide useful guidelines for better understanding the function of SCF/c‐kit in the self‐renewal and autophagy‐regulated mechanisms that promote of MSC survival. J. Cell. Biochem. 114: 79–88, 2012. © 2012 Wiley Periodicals, Inc. 相似文献
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通过RNA印迹分析和亚硝酸盐含量测定检查TNF-α、IL-1β和LPS对大鼠血管平滑肌细胞(VSMC)诱导型一氧化氮合酶(iNOS)基因表达及NO生成的影响.结果表明,TNF-α、IL-1β和LPS均能显著诱导VSMCiNOS基因表达和促进NO生成,其作用强度与浓度和作用时间有关;双因素(TNF-α+LPS,LPS+IL-1β)对诱导iNOS基因表达及NO生成产生协同作用.PolymyxinB和地塞米松可部分抑制TNF-α对iNOS基因表达的诱导作用及NO生成 相似文献
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Mary L. Taub IL Suk Yang Yue Wang 《In vitro cellular & developmental biology. Plant》1989,25(9):770-775
Summary A primary rabbit kidney epithelial cell culture system has been developed which retains differentiated functions of the renal
proximal tubule. In addition, the cells have a distinctive metabolism and spectrum of hormone responses. The primary cell
were observed to retain in vitro a Na+-dependent sugar transport system (distinctive of the proximal segment of the nephron) and a Na+-dependent phosphate transport system. Both of these transport processes are localized on the apical membrane of proximal
tubule cells in vivo. In addition, probenicid-sensitivep-aminohippurate (PAH) uptake was observed in basolateral membranes of the primary tubule cells, and the PAH uptake by these
vesicles occurred at a rate that was very similar to that observed with membranes derived from the original tissue. Several
other characteristics of the primary cells were examined, including hormone-sensitive cyclic AMP production and phosphoenolpyruvate
carboxykinase (PEPCK) activity. Like the cells in vivo, the primary proximal tubule cells were observed to produce significant
cyclic AMP in response to parathyroid hormone, but not in response to arginine vasopressin or salmon calcitonin. Significant
PEPCK acivity was observed in the particulate fraction derived from a homogenate of primary rabbit kidney proximal tubule
cells.
This paper was presented at a Symposium on the Physiology and Toxicology of the Kidney In Vitro co-sponsored by The Society
of Toxicology (SOT) and the Tissue Culture Association held at the 27th annual meeting of the SOT in Dallas, Texas in 1988.
This work was supported by Grant 9 RO1 DK40286-07 from the National Institutes of Health, Bethesda, MD, and NIH Research Career
Development Award 1 K04 CA 0088-01 to M.T. 相似文献
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Won IL Choi 《Journal of Asia》2011,14(2):227-231
Forest insect pests are one of the major disturbance factors in forest ecosystems and their outbreaks are expected to be more severe under the influence of global warming. Coleopterans are dominant among forest insects and their ecological functions include general detritivores, dead wood feeders, fungivores, herbivores, live wood feeders and predators. Ambrosia and bark beetles contribute to ecological succession of forests and, therefore, ecological functions of forests can be changed in response to their outbreaks. Mountain pine beetle (MPB) outbreaks are the most dramatic example of changes in the ecological functions of forest due to the outbreak of a forest insect pest altered by global warming. Composition of coleopteran species varies with latitude. However, composition of functional groups is consistent with latitude which indicates that resources available to beetles are consistent. In coleopteran communities, ambrosia and bark beetles can become dominant due to increases of dead or stressed trees due to the warming climate. This can also induce changes in the ecological functions of coleopterans, i.e. selective force to displace trees that have lower ecological fitness due to temperature increase. Therefore, recent increases in the density ambrosia and bark beetles offer a chance to study ecological processes in forests under the influence of global warming. 相似文献
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Dong‐Wook Kim Jung‐IL Chae Ji‐Young Kim Jhang Ho Pak Deog‐Bon Koo Young Yil Bahk Sang‐Beom Seo 《Journal of cellular biochemistry》2009,106(6):1048-1059
A nuclear phosphoprotein, DEK, is implicated in certain human diseases, such as leukemia and antoimmune disorders, and a major component of metazoan chromatin. Basically as a modulator of chromatin structure, it can involve in various DNA and RNA‐dependent processes and function as either an activator or repressor. Despite of numerous efforts to suggest the biological role of DEK, direct target proteins of DEK in different physiological status remains elusive. To investigate if DEK protein triggers the changes in certain protein networks, DEK was knocked down at both types of cell clones using siRNA expression. Here we provide a catalogue of proteome profiles in total cell lysates derived from normal HeLa and DEK knock‐down HeLa cells and a good in vitro model system for dissecting the protein networks due to this proto‐oncogenic DEK protein. In this biological context, we compared total proteome changes by the combined methods of two‐dimensional gel electrophoresis, quantitative image analysis and MALDI‐TOF MS analysis. There were a large number of targets for DEK, which were differentially expressed in DEK knock‐down cells and consisted of 58 proteins (41 up‐regulated and 17 down‐regulated) differentially regulated expression was further confirmed for some subsets of candidates by Western blot analysis using specific antibodies. In the identified 58 spots, 16% of proteins are known to be associated with apoptosis. Among others, we identified apoptosis related proteins such as Annexins, Enolase1, Lamin A, and Glutathione‐S‐transferase omega 1. These results are consistent with recent studies indicating the crucial role of DEK in apoptosis pathway. We further demonstrated by ChIP analysis that knock‐down of DEK caused hyperacetylation of histones around Prx VI promoter which is upregulated in our profile. Using immunoblotting analysis, we have demonstrated the modulation of other caspase‐dependent apoptosis related proteins by DEK knock‐down and further implicate its role in apoptosis pathway. J. Cell. Biochem. 106: 1048–1059, 2009. © 2009 Wiley‐Liss, Inc. 相似文献