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排序方式: 共有106条查询结果,搜索用时 62 毫秒
1.
T K Lebskaia N G Dolgikh G M Dubnitskaia K I Pakhomova L D Khobotilova 《Arkhiv anatomii, gistologii i émbriologii》1985,88(2):64-71
During initial stages freezing and conservation of Notothenia nudifrons L. muscle tissue are accompanied with nonspecific changes in the intracellular membranous system of fibers, in their lipid and protein composition. Certain connections between development of destructive changes in mitochondrial membranes, sarcoplasmic reticulum, T-system and intensity of accumulation of free fatty acids and products of peroxide oxydation of tissue lipids are revealed. Manifestation of hydrolitic enzymes activity coinsides, in time, with formation of autophage vacuoles. Transformation of the latter into residual bodies is in accord with a decreased enzymatic activity. A supposition is made concerning the mechanism of the muscle tissue destruction in the process of a prolonged conservation in cold. 相似文献
2.
mtDNA diversity in rhesus monkeys reveals overestimates of divergence time and paraphyly with neighboring species 总被引:4,自引:0,他引:4
Reconstructions of the human-African great ape phylogeny by using
mitochondrial DNA (mtDNA) have been subject to considerable debate. One
confounding factor may be the lack of data on intraspecific variation. To
test this hypothesis, we examined the effect of intraspecific mtDNA
diversity on the phylogenetic reconstruction of another Plio- Pleistocene
radiation of higher primates, the fascicularis group of macaque (Macaca)
monkey species. Fifteen endonucleases were used to identify 10 haplotypes
of 40-47 restriction sites in M. mulatta, which were compared with similar
data for the other members of this species group. Interpopulational,
intraspecific mtDNA diversity was large (0.5%- 4.5%), and estimates of
divergence time and branching order incorporating this variation were
substantially different from those based on single representatives of each
species. We conclude that intraspecific mtDNA diversity is substantial in
at least some primate species. Consequently, without prior information on
the extent of genetic diversity within a particular species, intraspecific
variation must be assessed and accounted for when reconstructing primate
phylogenies. Further, we question the reliability of hominoid mtDNA
phylogenies, based as they are on one or a few representatives of each
species, in an already depauperate superfamily of primates.
相似文献
3.
Correlation times in rotation diffusion of the radical in leaves and roots of wheat "Moskovskaya 35" were found under different conditions from the ESR spectra parameters of iminoxyl radical 2,2,6,6-tetramethyl-4-oxopiperidine-1-oxyl injected into these objects. The radical was shown to be transported along the plant with water current. Change of viscosity in dehydrated plant was studied. Temperature relationship (in the range 10-35 degrees C) of the probe surrounding in wheat leaves was investigated. A change of stabilizing effect of KCl admixture on the short-range order in water structure of the plants as compared to pure water was found. 相似文献
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Assembly of TbetaRI:TbetaRII:TGFbeta ternary complex in vitro with receptor extracellular domains is cooperative and isoform-dependent 总被引:4,自引:0,他引:4
Zúñiga JE Groppe JC Cui Y Hinck CS Contreras-Shannon V Pakhomova ON Yang J Tang Y Mendoza V López-Casillas F Sun L Hinck AP 《Journal of molecular biology》2005,354(5):1052-1068
Transforming growth factor-beta (TGFbeta) isoforms initiate signaling by assembling a heterotetrameric complex of paired type I (TbetaRI) and type II (TbetaRII) receptors on the cell surface. Because two of the ligand isoforms (TGFbetas 1, 3) must first bind TbetaRII to recruit TbetaRI into the complex, and a third (TGFbeta2) requires a co-receptor, assembly is known to be sequential, cooperative and isoform-dependent. However the source of the cooperativity leading to recruitment of TbetaRI and the universality of the assembly mechanism with respect to isoforms remain unclear. Here, we show that the extracellular domain of TbetaRI (TbetaRI-ED) binds in vitro with high affinity to complexes of the extracellular domain of TbetaRII (TbetaRII-ED) and TGFbetas 1 or 3, but not to either ligand or receptor alone. Thus, recruitment of TbetaRI requires combined interactions with TbetaRII-ED and ligand, but not membrane attachment of the receptors. Cell-based assays show that TbetaRI-ED, like TbetaRII-ED, acts as an antagonist of TGFbeta signaling, indicating that receptor-receptor interaction is sufficient to compete against endogenous, membrane-localized receptors. On the other hand, neither TbetaRII-ED, nor TbetaRII-ED and TbetaRI-ED combined, form a complex with TGFbeta2, showing that receptor-receptor interaction is insufficient to compensate for weak ligand-receptor interaction. However, TbetaRII-ED does bind with high affinity to TGFbeta2-TM, a TGFbeta2 variant substituted at three positions to mimic TGFbetas 1 and 3 at the TbetaRII binding interface. This proves both necessary and sufficient for recruitment of TbetaRI-ED, suggesting that the three different TGFbeta isoforms induce assembly of the heterotetrameric receptor complex in the same general manner. 相似文献
7.
Cvak L Jegorov A Sedmera P Císarová I Cejka J Kratochvíl B Pakhomova S 《Amino acids》2005,29(2):145-150
Summary. A novel natural peptide ergot alkaloid γ-ergokryptinine containing norleucine has been isolated from ergot sclerotia of the field-growing parasitic fungus Claviceps purpurea CCM 8059. Its structure was deduced from the NMR and mass spectral data. The final structural proof was provided by the crystal structure determination, which is the first X-ray structure of a natural Nle-containing secondary metabolite. The conformations of three ergopeptinines: γ-ergokryptinine, ergoladinine, and α-ergokryptinine were compared. 相似文献
8.
Walker K Pakhomova ON Kolb J Schoenbach KS Stuck BE Murphy MR Pakhomov AG 《Bioelectromagnetics》2006,27(3):221-225
The study explored the effect of ambient oxygen on mammalian cell survival after exposure to 10 ns duration, high voltage electrical pulses (nsEP, 80-90 or 120-130 kV/cm; 200-400 pulses per exposure). Cell samples were equilibrated with pure nitrogen, atmospheric air, or pure oxygen prior to the nsEP treatment and were returned to the incubator (air + 5% CO2) shortly after the exposure. The experiments established that survival of hypoxic Jurkat and U937 cells exceeded that of air-equilibrated controls about twofold (P < .01). Conversely, saturation of the medium with oxygen prior to exposure decreased Jurkat cell survival about 1.5 times, P < .01. Attenuation of the cytotoxic effect under hypoxic conditions resembled a well-known effect of oxygen on cell killing by sparsely ionizing radiations and may be indicative of the similarity of underlying cell damage mechanisms. 相似文献
9.
Oxidative effects of nanosecond pulsed electric field exposure in cells and cell-free media 总被引:2,自引:0,他引:2
ON Pakhomova VA Khorokhorina AM Bowman R Rodaitė-Riševičienė G Saulis S Xiao AG Pakhomov 《Archives of biochemistry and biophysics》2012,527(1):55-64
Nanosecond pulsed electric field (nsPEF) is a novel modality for permeabilization of membranous structures and intracellular delivery of xenobiotics. We hypothesized that oxidative effects of nsPEF could be a separate primary mechanism responsible for bioeffects. ROS production in cultured cells and media exposed to 300-ns PEF (1-13kV/cm) was assessed by oxidation of 2',7'-dichlorodihydrofluoresein (H(2)DCF), dihidroethidium (DHE), or Amplex Red. When a suspension of H(2)DCF-loaded cells was subjected to nsPEF, the yield of fluorescent 2',7'-dichlorofluorescein (DCF) increased proportionally to the pulse number and cell density. DCF emission increased with time after exposure in nsPEF-sensitive Jurkat cells, but remained stable in nsPEF-resistant U937 cells. In cell-free media, nsPEF facilitated the conversion of H(2)DCF into DCF. This effect was not related to heating and was reduced by catalase, but not by mannitol or superoxide dismutase. Formation of H(2)O(2) in nsPEF-treated media was confirmed by increased oxidation of Amplex Red. ROS increase within individual cells exposed to nsPEF was visualized by oxidation of DHE. We conclude that nsPEF can generate both extracellular (electrochemical) and intracellular ROS, including H(2)O(2) and possibly other species. Therefore, bioeffects of nsPEF are not limited to electropermeabilization; concurrent ROS formation may lead to cell stimulation and/or oxidative cell damage. 相似文献
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