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71.
Takahashi M Yokoe S Asahi M Lee SH Li W Osumi D Miyoshi E Taniguchi N 《Biochimica et biophysica acta》2008,1780(3):520-524
More and more evidence indicates that N-glycan regulates signal transduction by modulating receptor functions. Previous studies suggested that glycosylation of EGFR is involved in dimerization and endocytosis. We further determined the role of N-glycosylation of ErbB family. A series of human ErbB3 mutants that lack each of the 10 N-glycosylation sites were prepared and transfected to Flp-In-CHO cells for stable expression. A crosslinking study showed that Asn 418 to Gln mutant (N418Q) of ErbB3 underwent autodimerization without its ligand, heregulin, and the heterodimer formation with ErbB2 was also increased. The N418Q mutant of ErbB3 co-expressed with ErbB2 promoted downstream signaling, anchorage-independent cell growth and the tumor growth in athymic mice. These findings suggest that the specific N-glycan in domain III of ErbB family plays an essential role in regulating receptor dimerization and transforming activity. We assume that the N-glycans affect the conformation of ErbB family, which is crucial for their activity. Together with findings from other laboratories, it is suggested that N-glycosylation controls ErbB signaling by various mechanisms. 相似文献
72.
Yamochi T Ohnuma K Hosono O Tanaka H Kanai Y Morimoto C 《Biochemical and biophysical research communications》2008,370(1):195-199
We identified human decapping enzyme 2 (hDCP2) as a binding protein with Ro52, being colocalized in processing bodies (p-bodies). We also showed that the N-terminus and C-terminus of Ro52 bound to hDCP2. Moreover, Ro52 enhanced decapping activity of hDCP2 in a dose-dependent manner. Our data support the novel notion of the association between Ro52 with hDCP2 protein in cytoplasmic p-bodies, playing a role in mRNA metabolism in response to cellular stimulation. 相似文献
73.
Ishihara K Kitamura H Hiraizumi K Kaneko M Takahashi A Zee O Seyama T Hong J Ohuchi K Hirasawa N 《Biochemical and biophysical research communications》2008,366(4):1007-1011
The constitutively activated tyrosine kinase Fip1-like 1 (FIP1L1)-platelet-derived growth factor receptor α (PDGFRα) causes eosinophilic leukemia EoL-1 cells to proliferate. Recently, we demonstrated that histone deacetylase inhibitors suppressed this proliferation and induced the differentiation of EoL-1 cells into eosinophils in parallel with a decrease in the level of FIP1L1-PDGFRα. In this study, we analyzed the mechanism by which FIP1L1-PDGFRα induces the proliferation and whether the suppression of cell proliferation triggers the differentiation into eosinophils. The FIP1L1-PDGFRα inhibitor imatinib inhibited the proliferation of EoL-1 cells and decreased the level of the oncoprotein c-Myc as well as the phosphorylation of extracellular signal-regulated kinase and c-Jun N-terminal kinase (JNK). The proliferation of EoL-1 cells and expression of c-Myc were also inhibited by the MEK inhibitor U0126 and JNK inhibitor SP600125. The expression of the eosinophilic differentiation marker CCR3 was not induced by imatinib. These findings suggest that FIP1L1-PDGFRα induces the proliferation of EoL-1 cells through the induction of c-Myc expression via ERK and JNK signaling pathways, but is not involved in the inhibition of differentiation toward mature eosinophils. 相似文献
74.
Nie X Nishitani C Yamazoe M Ariki S Takahashi M Shimizu T Mitsuzawa H Sawada K Smith K Crouch E Nagae H Takahashi H Kuroki Y 《Biochemistry》2008,47(48):12878-12885
Pulmonary surfactant protein D (SP-D) is a member of the collectin family and plays crucial roles in the innate immunity of the lung. We have previously shown that surfactant protein A (SP-A), a homologous collectin, interacts with MD-2 and alters lipopolysaccharide signaling. In this study, we examined and characterized the binding of SP-D to MD-2 using a soluble form of recombinant MD-2 (sMD-2). SP-D bound in a concentration- and Ca(2+)-dependent manner to sMD-2 coated onto microtiter wells. Excess mannose abolished the binding of SP-D to sMD-2. In solution, SP-D cosedimented with sMD-2 in the presence of Ca(2+). The direct binding of SP-D to sMD-2 was confirmed by BIAcore analysis. Anti-SP-D monoclonal antibody that recognizes the carbohydrate recognition domain (CRD) of SP-D significantly inhibited the binding of SP-D to sMD-2, indicating the involvement of the CRD for the binding to sMD-2. Ligand blot analysis revealed that SP-D bound to N-glycopeptidase F-treated sMD-2. In addition, the biotinylated SP-D pulled down the mutant sMD-2 with Asn(26) --> Ala and Asn(114) --> Ala substitutions, which lacks the consensus for N-glycosylation. Furthermore, the sMD-2 mutant cosedimented SP-D. These results demonstrate that SP-D directly interacts with MD-2 through the CRD. 相似文献
75.
Regulation of stress-activated protein kinase signaling pathways by protein phosphatases. 总被引:5,自引:0,他引:5
Shinri Tamura Masahito Hanada Motoko Ohnishi Koji Katsura Masato Sasaki Takayasu Kobayashi 《European journal of biochemistry》2002,269(4):1060-1066
Stress-activated protein kinase (SAPK) signaling plays essential roles in eliciting adequate cellular responses to stresses and proinflammatory cytokines. SAPK pathways are composed of three successive protein kinase reactions. The phosphorylation of SAPK signaling components on Ser/Thr or Thr/Tyr residues suggests the involvement of various protein phosphatases in the negative regulation of these systems. Accumulating evidence indicates that three families of protein phosphatases, namely the Ser/Thr phosphatases, the Tyr phosphatases and the dual specificity Ser/Thr/Tyr phosphatases regulate these pathways, each mediating a distinct function. Differences in substrate specificities and regulatory mechanisms for these phosphatases form the molecular basis for the complex regulation of SAPK signaling. Here we describe the properties of the protein phosphatases responsible for the regulation of SAPK signaling pathways. 相似文献
76.
Three-week-old DDD mice were easily rendered tolerant to human IgG while 12-week-old mice were tolerized only partially. Mechanisms of the development of the resistance with age were investigated. It was shown by the cell transfer experiments that spleen T cells, purified on a Tetron wool column, from older mice were responsible for the resistance, which was not associated with the loss of suppressor cells with age. To elucidate the possibility of whether tolerogen-sensitive spleen T cells differentiate into resistant ones, cell transfer experiments were carried out in which thymectomized, lethally irradiated mice were reconstituted with spleen cells from 3-week-old mice and then treated with the tolerogen on various days afterward. The results indicated that tolerance was inducible in these hosts to the same degree, irrespective of the timing of the tolerogen injection, while age-matched intact mice gradually acquired the resistance. Then the possibility of whether age of thymus affected tolerance inducibility of the hosts or not was examined. The tolerogen was injected into irradiated, bone-marrow-reconstituted mice which bore either 4- or 7-week-old thymus. It was shown that helper T cells newly generated under younger thymus acquired higher susceptibility to the tolerogen. There was no difference in tolerance inducibility irrespective as to whether bone marrow cells were prepared from younger or older mice. From these observations it was suggested that the resistance to tolerance induction in DDD mice is acquired through the appearance of resistant T cells which are generated from T-cell precursors in bone marrow under the influence of a radioresistant thymic constitution and predominantly located in the spleen. 相似文献
77.
Kazuhiko S.K. Uchida Minji Jo Kota Nagasaka Motoko Takahashi Norihisa Shindo Katsushi Shibata Kozo Tanaka Hiroshi Masumoto Tatsuo Fukagawa Toru Hirota 《Current biology : CB》2021,31(8):1581-1591.e3
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78.
Hideharu Miura Shuichi Ozawa Takaaki Matsuura Atsushi Kawakubo Fumika Hosono Kiyoshi Yamada Yasushi Nagata 《Reports of Practical Oncology and Radiotherapy》2018,23(3):183-188
Purpose
The purpose of this study was to verify whether the dynamic tumor tracking (DTT) feature of a Vero4DRT system performs with 10-mm-long and 0.28 mm diameter gold anchor markers.Methods
Gold anchor markers with a length of 10 mm and a diameter of 0.28 mm were used. Gold anchor markers were injected with short and long types into bolus material. These markers were sandwiched by a Tough Water (TW) phantom in the bolus material. For the investigation of 4-dimensional (4D) modeling feasibility under various phantom thicknesses, the TW phantom was added at 2 cm intervals (in upper and lower each by 1 cm). A programmable respiratory motion table was used to simulate breathing-induced organ motion, with an amplitude of 30 mm and a breathing cycle of 3 s. X-ray imaging parameters of 80 kV and 125 kV (320 mA and 5 ms) were used. The least detection error of the fiducial marker was defined as the 4D-modeling limitation.Results
The 4D modeling process was attempted using short and long marker types and its limitation with the short and long types was with phantom thicknesses of 6 and 10 cm at 80 kV and 125 kV, respectively. However, the loss in detectability of the gold anchor because of 4D-modeling errors was found to be approximately 6% (2/31) with a phantom thickness of 2 cm under 125 kV. 4D-modeling could be performed except under the described conditions.Conclusions
This work showed that a 10-mm-long gold anchor marker in short and long types can be used with DTT for short water equivalent path length site, such as lung cancer patients, in the Vero4DRT system. 相似文献79.
Effect of gas pressure in the root and stem base zone on methane transport through rice bodies 总被引:3,自引:0,他引:3
Ebullition of gas bubbles from the soil surface is, in some cases (e.g., in early growth stage of rice), one of the major pathways for methane transport from rice paddies to the atmosphere. However, the role of the gas phase (entrapped gas) in the paddy soil in plant-mediated methane transport, which is the major pathway for methane emission, has not been clarified. To clarify the effect of the gas phase below ground on the methane emission rate through rice plants, we partly exposed the root and stem base of hydroponically grown rice to a high concentration of methane gas at various gas pressures, and immersed the rest of the roots in a solution with a high methane concentration. The methane emission rate was measured from the top of the rice plant using a flow-through chamber method. The methane emission rate drastically increased with a small increase in gas pressure in the gas phase at the root and stem base zone, with about a 3 times larger emission rate being observed with 10 × 10-3 atm of extra pressure (corresponding to 10 cm of standing water in rice paddy) compared to no extra pressure. However, when alginate was applied to the stem near the base to prevent contact with the gas phase, the methane emission rate did not increase with increasing gas pressure. On the other hand, from observations in the rice paddy, it was found that the gas is entrapped near the surface (e.g., at a depth of 1 cm) and the gas entrapped in the soil would come into direct contact with a part of the stem near the base of the rice plant. Thus, the gas entrapped in the soil could enter into the rice body directly from the part of the stem near the base which is beneath the soil surface due to gas pressure in the gas phase resulting from the pressure exerted by the standing water. Hence, this mechanism involving the entrapped gas could play an important role in methane emission from rice paddy by affecting the plant-mediated methane transport as well as ebullition of gas bubbles. 相似文献
80.
Large diurnal and seasonal variations in methane flux from rice paddies have been found in many studies. Although these variations are considered to result from changes in methane formation rates in the soil and the transport capacity (e.g. biomass, physiological activities, and so on) of rice plants, the real reasons for such variations are as yet unclear. This study was conducted to clarify the effects of temperature on the rate of methane transport from the root zone to the atmosphere using hydroponically grown rice plants. Methane emission rates from the top of the rice plants whose roots were soaked in a solution with a high methane concentration were measured using a flow-through chamber method with the top or root of the rice plants being kept at various temperatures. The methane emission rates and methane concentrations in solution were analyzed using a diffusion model which assumes that the methane emission from a rice paddy is driven by molecular diffusion through rice plants by a concentration gradient. In the experiment where the temperature around the root was changed, the conductance for methane diffusion was typically 2.0-2.2 times larger when the solution temperature was changed from 15 to 30 °C. When the air temperature surrounding the top of the rice plant was changed, the change in conductance was much less. In addition, from measurements of methane flux and methane concentration in soil water in a lysimeter rice paddy during the 2 growing seasons of rice, it was found that the conductance for methane transport was correlated with the soil temperature at 5 cm depth. These results suggest that the temperature around the root greatly affects the methane transport process in rice plants, and that the process of passing through the root is important in determining the rate of methane transport through rice plants. 相似文献