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141.
142.
Ryo Kodama Masayoshi Kato Shuichi Furuta Shouta Ueno Yugen Zhang Kuniharu Matsuno Chihiro Yabe‐Nishimura Eiji Tanaka Tohru Kamata 《Genes to cells : devoted to molecular & cellular mechanisms》2013,18(1):32-41
Activated oncogenes induce premature cellular senescence, a permanent state of proliferative arrest in primary rodent and human fibroblasts. Recent studies suggest that generation of reactive oxygen species (ROS) is involved in oncogenic Ras‐induced premature senescence. However, the signaling mechanism controlling this oxidant‐mediated irreversible growth arrest is not fully understood. Here, we show that through the Ras/MEK pathway, Ras oncogene up‐regulated the expression of superoxide‐generating oxidases, Nox1 in rat REF52 cells and Nox4 in primary human lung TIG‐3 cells, leading to an increase in intracellular level of ROS. Ablation of Nox1 and Nox4 by small interfering RNAs (siRNAs) blocked the RasV12 senescent phenotype including β‐galactosidase activity, growth arrest and accumulation of tumor suppressors such as p53 and p16Ink4a. This suggests that Nox‐generated ROS transduce senescence signals by activating the p53 and p16Ink4a pathway. Furthermore, Nox1 and Nox4 siRNAs inhibited both Ras‐induced DNA damage response and p38MAPK activation, whereas overexpression of Nox1 and Nox4 alone was able to induce senescence. The involvement of Nox1 in Ras‐induced senescence was also confirmed with embryonic fibroblasts derived from Nox1 knockout mice. Together, these findings suggest that Nox1‐ and Nox4‐generated ROS play an important role in Ras‐induced premature senescence, which may involve DNA damage response and p38MAPK signaling pathways. 相似文献
143.
The development of new technologies for securing and recycling water resources are in high demand. A key focus of these technologies is the development of various ion exchangers or adsorbents that are used for the purification of aqueous solutions. Layered sodium titanate is one of the cation exchangers utilised in the removal of heavy metals and radionuclides from wastewater. To enhance the removal efficiency, the precise design of the crystal morphology, structure, and chemical composition is important. Herein, we synthesised a unique seaweed-like sodium titanate mat (SST) using a template-free alkaline hydrothermal process. The Co2+ sorption capacity of SST was investigated by batch testing with cobalt(ii) nitrate. SST, which was synthesised from titanium sulphate in a 10 M NaOH solution at 200 °C, had a seaweed-like structure composed of randomly distributed nanofibres of layered sodium titanate that is approximately 9 nm in diameter. The crystal shape changed from roundish crystals to fibrous crystals as the hydrothermal reaction period increased. The Co2+ sorption isotherm of SST was fitted with the Langmuir isotherm model and the maximum sorption density was 1.85 mmol g−1. The selectivity of the Co2+ sorption on SST was high in comparison to that of Ca2+ and Mg2+. Herein, the Co2+ sorption mechanisms of SST were studied in comparison with commercially available sodium titanate. Results show that controlling the crystal morphology, structure, and Na concentration of the layered titanate that can be ion-exchanged determines the cation sorption properties of sodium titanate.The seaweed-like sodium titanate mat has a high Co2+ sorption capacity via the ion-exchange reaction due to its crystal structure, low crystallinity, and morphology. 相似文献
144.
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146.
Kujiraoka T Hattori H Ito M Nanjee MN Ishihara M Nagano M Iwasaki T Cooke CJ Olszewski WL Stepanova IP Egashira T Miller NE 《Atherosclerosis》2004,176(1):57-62
We have previously shown that intravenous apolipoprotein (apo) A-I/phosphatidylcholine (apo A-I/PC) discs increase plasma high-density lipoprotein (HDL) concentration in humans. We have now studied the associated changes in two enzymes, paraoxonase (PON) and platelet-activating factor acetylhydrolase (PAF-AH) that are carried in whole or in part by HDLs, and are thought to influence atherogenesis by hydrolyzing oxidized phospholipids in lipoproteins. Apo A-I/PC discs (40 mg/kg over 4 h) were infused into eight healthy males. Although plasma apo A-I and HDL cholesterol increased on average by 178 and 158%, respectively, plasma total PON and total PAF-AH concentrations did not rise. By the end of the infusion, HDL-associated PAF-AH had increased by 0.56 +/- 0.14 microg/mL (mean +/- S.D., P < 0.01), and nonHDL-associated PAF-AH had decreased by 0.84 +/- 0.11 microg/mL (P < 0.05). These changes were accompanied by an increase in the HDL-associated PAF-AH/apo A-I ratio from 0.19 to 0.35 (P < 0.05), and by a decrease in the nonHDL-associated PAF-AH/apo B ratio from 2.1 to 1.4 (P < 0.05). No changes in PON or PAF-AH concentrations were detected in prenodal lymph (tissue fluid), collected continuously from the leg. Our results show that the total concentrations of PON and PAF-AH in plasma are uninfluenced by plasma HDL concentration. PAF-AH transfers readily between HDLs and LDLs in vivo, and its distribution between them is determined partly by their relative concentrations and partly by HDL composition. 相似文献
147.
Tohru Minamino Yusuke V. Morimoto Miki Kinoshita Keiichi Namba 《Proceedings of the National Academy of Sciences of the United States of America》2021,118(22)
The proton motive force (PMF) consists of the electric potential difference (Δψ), which is measured as membrane voltage, and the proton concentration difference (ΔpH) across the cytoplasmic membrane. The flagellar protein export machinery is composed of a PMF-driven transmembrane export gate complex and a cytoplasmic ATPase ring complex consisting of FliH, FliI, and FliJ. ATP hydrolysis by the FliI ATPase activates the export gate complex to become an active protein transporter utilizing Δψ to drive proton-coupled protein export. An interaction between FliJ and a transmembrane ion channel protein, FlhA, is a critical step for Δψ-driven protein export. To clarify how Δψ is utilized for flagellar protein export, we analyzed the export properties of the export gate complex in the absence of FliH and FliI. The protein transport activity of the export gate complex was very low at external pH 7.0 but increased significantly with an increase in Δψ by an upward shift of external pH from 7.0 to 8.5. This observation suggests that the export gate complex is equipped with a voltage-gated mechanism. An increase in the cytoplasmic level of FliJ and a gain-of-function mutation in FlhA significantly reduced the Δψ dependency of flagellar protein export by the export gate complex. However, deletion of FliJ decreased Δψ-dependent protein export significantly. We propose that Δψ is required for efficient interaction between FliJ and FlhA to open the FlhA ion channel to conduct protons to drive flagellar protein export in a Δψ-dependent manner.The ion motive force (IMF) across the cell membrane is one of the most important sources of biological energy in any cell. The IMF is utilized for many essential biological activities, such as ATP synthesis, solute transport, nutrient uptake, protein secretion, flagella-driven motility, and so on (1). The IMF is the sum of the electrical (Δψ) and chemical (ΔpI) potential differences of ions such as protons (H+) (the proton motive force [PMF]) and sodium ions (Na+) (the sodium motive force [SMF]) across the membrane and is defined by Eq. 1:[1]where Vm is Δψ; [ion]in and [ion]ex are the internal and external ion concentrations, respectively; kB is Boltzmann’s constant; T is the absolute temperature (in kelvins); and q is the charge of the ion. The Δψ corresponds to the membrane voltage (2).The flagellum of the enteric bacterium Salmonella enterica serovar Typhimurium (hereafter referred to as Salmonella) is a supramolecular motility machine consisting of the basal body, which acts as a bidirectional rotary motor; the hook, which functions as a universal joint; and the filament, which works as a helical propeller. The Salmonella flagellar motor is powered by a PMF across the cytoplasmic membrane. The motor consists of a rotor and multiple stator units, each of which acts as a transmembrane proton channel complex. The stator unit converts the proton influx through the channel into the force for high-speed rotation of the long helical filament (3, 4).For construction of the hook and filament structures at the cell exterior, a specialized protein transporter utilizes the PMF to transport flagellar building blocks to the distal end of the growing flagellar structure. The flagellar protein transporter consists of a PMF-driven export gate complex made of five transmembrane proteins, FlhA, FlhB, FliP, FliQ, and FliR, and an ATPase ring complex consisting of three cytoplasmic proteins, FliH, FliI, and FliJ (SI Appendix, Fig. S1) (5, 6). These proteins are evolutionarily related to those of the virulence-associated type III secretion systems of pathogenic bacteria, which inject effector proteins into eukaryotic host cells for invasion (7). Furthermore, the entire structure of the ATPase ring complex is structurally similar to the cytoplasmic F1 part of FOF1-ATP synthase, which utilizes the PMF for ATP synthesis (8–10).FliI forms a homo-hexamer that hydrolyzes ATP at an interface between neighboring FliI subunits (10–12). FliJ binds to the central pore of the FliI ring (9). ATP hydrolysis by the FliI ATPase not only activates the transmembrane export gate complex through an interaction between FliJ and the C-terminal cytoplasmic domain of FlhA (FlhAC) (13, 14) but also opens the entrance gate of the polypeptide channel through an interaction between FliI and the C-terminal cytoplasmic domain of FlhB (FlhBC) (15). As a result, the export gate complex becomes an active proton/protein antiporter that couples an inward-directed H+ flow with an outward-directed protein export (SI Appendix, Fig. S1) (16). When the cytoplasmic ATPase complex becomes nonfunctional, the FlgN chaperone activates the Na+-driven export engine of the export gate complex over a wide range of external pH, allowing the export gate complex to drive Na+-coupled protein export (17, 18). The transmembrane domain of FlhA (FlhATM) acts as a transmembrane ion channel for the transit of both H+ and Na+ across the cytoplasmic membrane (17).A chemical potential gradient of either H+ (ΔpH) or Na+ (ΔpNa) is required for efficient inward-directed translocation of H+ or Na+ when FliH and FliI are absent (13, 17). Although the Δψ component is critical for flagellar protein export by the wild-type export gate complex (19), it remains unknown when and how Δψ is used for the flagellar protein export process. To clarify this question, we used the Salmonella MMHI0117 [ΔfliH-fliI flhB(P28T)] strain (hereafter referred to as ΔHI B*; Table 1) (20), in which the export gate complex uses both Δψ and ΔpNa at different steps of the flagellar protein export process (13, 17). We show that an increase in Δψ generated by an upward shift of the external pH from 7.0 to 8.5 activates flagellar protein export by this mutant even in the absence of ΔpNa, suggesting the presence of a Δψ-dependent activation mechanism for proton-coupled protein secretion by the export gate complex. We also show that an increased Δψ facilitates efficient docking of FliJ to FlhAC.Table 1.Summary for flagellar protein export properties of Salmonella strains used in this study
Open in a separate window 相似文献
Strains | Abbreviated name | External pH | FlgD secretion |
SJW1103 (wild type) | WT | 7.0 | ++++ |
7.5 | +++++ | ||
8.0 | +++++ | ||
8.5 | +++++ | ||
MMHI0117 (ΔfliHI flhB*) | ΔHI B* | 7.0 | +/− |
7.5 | + | ||
8.0 | ++++ | ||
8.5 | +++++ | ||
NH004 (ΔfliHI flhB* ΔflhA) | ΔHI B* ΔA | 7.0 | — |
7.5 | — | ||
8.0 | — | ||
8.5 | — | ||
MMHI0017-3 [ΔfliHI flhB* flhA(T490M)] | ΔHI B* A* | 7.0 | +++++ |
7.5 | +++++ | ||
8.0 | +++++ | ||
8.5 | +++++ | ||
MMHIJ0117 (ΔfliHIJ flhB*) | ΔHIJ B* | 7.0 | — |
7.5 | — | ||
8.0 | +/− | ||
8.5 | + | ||
MMHIJ0117-3 [ΔfliHIJ flhB* flhA(T490M)] | ΔHIJ B* A* | 7.0 | +++++ |
7.5 | +++++ | ||
8.0 | +++++ | ||
8.5 | +++++ |
148.
Motoyasu Ishii Yutaka Miyazaki Takeshi Yamamoto Masahito Miura Yoshiyuki Ueno Tohru Takahashi Takayoshi Toyota 《Liver international》1993,13(4):227-231
ABSTRACT— A 50-year-old woman suffered from a diffuse skin rash, high fever and jaundice immediately after a second injection of glutathion and Stronger Neo-minophagen C which contains glycyrrhizin. Liver biopsy performed 11 months after the onset showed mild spotty hepatocyte necrosis, marked cholestasis in parenchyma, and some lymphocyte infiltration in the portal area. Interlobular bile ducts had undergone vacuolar degeneration or were absent in some portal tracts. In her hospital course, unremitting jaundice persisted and biliary cirrhosis developed with signs of portal hypertension; she died from liver failure 26 months after the onset. A liver specimen at her death revealed that most of the interlobular bile ducts had vanished. Based on the clinical course and pathology, drug-induced ductopenia, possibly due to an adverse reaction to glycyrrhizin, is the most likely diagnosis. While drug-related biliary cirrhosis is rarely fatal, this case presented an unusually rapid course of fatal biliary cirrhosis. 相似文献
149.
Tatsuro Wakayama M.D. Tohru Itoh M.D. Yasushi Takeda M.D. Tomoo Kosuge M.D. Kazuaki Shimada M.D. Yuji Nomura M.D. Kazuyuki Shimomura M.D. Yasuo Idezuki M.D. F.A.C.S. 《The American journal of gastroenterology》1990,85(9):1168-1171
We report the successful treatment of bilateral intrahepatic biliary stones by endoscopic electrohydraulic lithotripsy (EHL). EHL is a useful procedure by which large stones can be fragmented easily and complete removal of stones can be attained. 相似文献
150.
Seiji Kawamura Yasuo Ono Tetsuro Kamiya Yoshio Arakaki Tohru Nakajima Yoshihisa Kinoshita Muneo Yoshibayashi Toshikatsu Yagihara 《Heart and vessels》1995,10(4):214-217
Summary Between August 1985 and July 1992, at our center, 142 Japanese children had an extracardiac conduit operation to reconstruct the right ventricular outflow tract. The study group consisted of 22 of these 142 children who had a persistent fever and whose serum was positive for acute-phase reactants after the operation. We present the diagnostic findings for 10 children with infection of an extracardiac conduit that had been placed to restore the continuity of the right ventricle-pulmonary artery. They were part of the group of 22 children who were followed over the past 7 years with blood cultures, echocardiography, and67Ga imaging. All 10 developed a persistent fever and were seropositive for acute-phase reactants. Conduit infection was diagnosed in only 2 patients by the detection of vegetation on echocardiography and was diagnosed in 9 of the 10 patients by an abnormal67Ga uptake in the area of the artificial vessels used to reconstruct the pulmonary artery. The present study compared the use of blood cultures, echocardiography, and67Ga imaging in diagnosing an infection of the extracardiac conduit. The sensitivity of blood cultures in diagnosing an extracardiac conduit infection was 70% (7/10), and the specificity was 92% (1/12).67Ga imaging showed a higher sensitivity than echocardiography in diagnosing infection of an extracardiac conduit. 相似文献