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1.
J Environ Radioact ; 272: 107354, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38086286

ABSTRACT

Particulate matter trapped by tufts of water moss Fontinalis antipyretica inhabiting fast flowing waters of the Yenisei River (Siberia, Russia) contaminated with artificial radionuclides has been studied as a potential monitor of radioactive releases to the river. Particulate matter, which was removed from wet tufts of water moss of the Yenisei by rinsing them in water, constituted at least 38% of bulk dry weight of the moss biomass sample and was similar in the contents of chemical elements, minerals, organic matter, and artificial radionuclides to bottom sediments of the Yenisei. Considerable bulk percentages of artificial radionuclides in the sample of water moss, 77% of 137Cs, 44% of 60Co, 41% of 152Eu, 55% of 154Eu, 66% of 241Am, and 34-36% of plutonium were associated with extracellular particles. The comparative study and correlation analysis suggested that 137Cs was mainly associated with mineral particles trapped by moss and that organic matter was responsible for binding plutonium in samples of water moss. Consequently, analysis of extracellular particles of water moss can provide data on contents and speciation of radionuclides transported by water current. Although a considerably high proportion of particulate matter had been washed out from tufts of water moss, some extracellular mineral particulate material and a large number of epiphytic diatoms remained attached to leaves of water moss. Our study proves that particulate matter trapped by water moss can be used as an informative monitor to trace radioactive pollutants transported by water current in running waters deficient in bottom sediments and potential biomonitors.


Subject(s)
Plutonium , Radiation Monitoring , Water Pollutants, Radioactive , Rivers/chemistry , Water , Particulate Matter/analysis , Plutonium/analysis , Water Pollutants, Radioactive/analysis , Cesium Radioisotopes/analysis , Minerals/analysis , Geologic Sediments
2.
Cell Tissue Res ; 340(3): 437-50, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20512590

ABSTRACT

Two dozen hybrid clones were produced by fusion of diploid embryonic stem (ES) cells positive for green fluorescent protein (GFP) with tetraploid fibroblasts derived from DD/c and C57BL-I(I)1RK mice. Cytogenetic analysis demonstrated that most cells from these hybrid clones contained near-hexaploid chromosome sets. Additionally, the presence of chromosomes derived from both parental cells was confirmed by polymerase chain reaction (PCR) analysis of polymorphic microsatellites. All hybrid cells were positive for GFP and demonstrated growth characteristics and fibroblast-like morphology. In addition, most hybrid cells were positive for collagen type I, fibronectin, and lamin A/C but were negative for Oct4 and Nanog proteins. Methylation status of the Oct4 and Nanog gene promoters was evaluated by bisulfite genomic sequencing analysis. The methylation sites (CpG-sites) of the Oct4 and Nanog gene promoters were highly methylated in hybrid cells, whereas the CpG-sites were unmethylated in the parental ES cells. Thus, the fibroblast genome dominated the ES genome in the diploid ES cell/tetraploid fibroblast hybrid cells. Immunofluorescent analysis of the pluripotent and fibroblast markers demonstrated that establishment of the fibroblast phenotype occurred shortly after fusion and that the fibroblast phenotype was further maintained in the hybrid cells. Fusion of karyoplasts and cytoplast derived from tetraploid fibroblasts with whole ES cells demonstrated that karyoplasts were able to establish the fibroblast phenotype of the reconstructed cells but not fibroblast cytoplasts. Thus, these data suggest that the dominance of parental genomes in hybrid cells of ES cell/somatic cell type depends on the ploidy of the somatic partner.


Subject(s)
Embryonic Stem Cells/metabolism , Fibroblasts/metabolism , Genome/genetics , Hybrid Cells/metabolism , Ploidies , Animals , Base Sequence , Chromosomes, Mammalian/metabolism , Collagen Type I/genetics , Collagen Type I/metabolism , DNA Methylation/genetics , Embryonic Stem Cells/cytology , Embryonic Stem Cells/ultrastructure , Fibroblasts/cytology , Fibroblasts/ultrastructure , Fibronectins/genetics , Fibronectins/metabolism , Fluorescent Antibody Technique , Gene Expression Regulation , Homeodomain Proteins/metabolism , Hybrid Cells/cytology , Hybrid Cells/ultrastructure , Lamin Type A/metabolism , Mice , Molecular Sequence Data , Nanog Homeobox Protein , Octamer Transcription Factor-3/metabolism
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