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Latest Paper:

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Assembly and directed orientation of anisotropic particles with an external AC electric field in a range of 1 kHz to 2 MHz were studied for asymmetric composite dumbbells incorporating a silica, titania or titania/silica (titania:silica=75:25 vol%) sphere. The asymmetric composite dumbbells, which were composed of a polymethylmethacrylate(PMMA)-coated sphere (core-shell part) and a polystyrene (PSt) lobe, were synthesized with a soap-free emulsion polymerization to prepare PMMA-coated inorganic spheres and another soap-free emulsion polymerization to form a polystyrene (PSt) lobe from the PMMA-coated inorganic spheres. The composite dumbbells dispersed in water were directly observed with optical microscopy. The dumbbells incorporating a silica sphere oriented parallel to an electric field in the whole frequency range, and they formed pearl chain structure at a high frequency of 2 MHz. The titania-incorporated dumbbells formed chain structures, in which they contacted their core-shell parts and oriented perpendicularly to a low-frequency (kHz) field whereas they oriented parallel to a high-frequency (MHz) field. Since the alignment of dumbbells in the chains depends not only on the interparticle forces but also on the torque that the induced dipoles in the dumbbells experience in the electric field, the orientation of dumbbells perpendicularly to the electric field was the case dominated by the interparticle force whereas the other orientation was the case dominated by the torque. The present experiments show that the incorporation of inorganic dumbbells is an effective way to control the assembled structure and orientation with an electric field.
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Department of Pediatrics.
Human bocavirus (HBoV) 1, 2, 3 and 4 were detected in 132 (15.5%), 5 (0.6%), 3 (0.4%) and 5 (0.6%) of 850 nasopharyngeal swab samples collected from children with respiratory tract infections, respectively. Out of the 145 HBoV1-4-positive samples, 62 (42.8%) were co-detected with other respiratory viruses.
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Division of Preventive Oncology, Department of Oncology, Faculty of Medicine, University of Calgary, Calgary, AB, Canada.
Every year, approximately 25,000 patients are diagnosed with oral cavity squamous cell carcinoma (OCSCC) in the USA. The 5-year survival rate for OCSCC is approximately 40%. Intratumoral hypoxia confers poor prognosis and treatment failure but direct tumor oxygen measurement is challenging. Carbonic anhydrase IX (CAIX) is a marker of tissue hypoxia and we have recently shown that stromal CAIX is associated with reduced survival in patients with HPV-negative head and neck cancer. We examined the importance of this observation in OCSCC patients. We identified patients diagnosed and treated with OCSCC in Calgary (Alberta, Canada) between 1998 and 2005. Clinical and pathologic data were obtained from the Alberta Cancer Registry and chart review. Tissue microarrays (TMAs) were assembled from triplicate cores of archived tumor tissue. Stromal CAIX expression was assessed by quantitative immunohistochemistry (AQUA-HistoRx). The primary endpoint was disease-specific survival. We identified 102 patients with OCSCC; 87 patients had surgery as their primary treatment and adequate tumor tissue for TMA construction was available for all patients. CAIX expression was evaluable for 61 patients. High (top quartile) stromal CAIX expression was associated with significantly reduced 5-year disease-specific survival compared to low stromal CAIX expression (p<0.006). This study confirms our previously reported association between high stromal CAIX expression and significantly reduced overall survival in an independent, predominantly p16-negative, cohort of surgically treated OCSCC. Assessment of stromal CAIX expression could identify patients with the least favorable prognosis and inform therapeutic strategies in OCSCC.
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Department of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.
Microglia are intrinsic immune cells in the brain. In response to neurodegenerative events, excessively activated microglia change their shapes and release various cytokines leading to the pathogenesis of central nervous system (CNS) disease. Because the intracellular mechanisms of this process are still unclear, we have evaluated the functional roles of transient receptor potential vanilloid 4 (TRPV4) channel expressed in the microglia. Robust microglial activation after an injection of lipopolysaccharide (LPS) into the mouse cerebral ventricle was suppressed by concurrent administration of a selective TRPV4 agonist, 4α-phorbol 12,13-didecanoate (4α-PDD). When the mechanism was further investigated using cultured rat microglia intrinsically expressing functional TRPV4, release of tumor necrosis factor-α (TNF-α) and expression of galectin-3 were both increased by LPS. These increases were significantly suppressed by cotreatment with 4α-PDD, and the inhibitory effects of 4α-PDD were abolished by knockdown of TRPV4 or TRPV4 antagonists. The amplitude of voltage-dependent K(+) current, which is augmented during microglial activation, was also suppressed by 4α-PDD treatment. Opening of TRPV4 channels with 4α-PDD induced membrane depolarization mainly by increasing Na(+) influx. In addition, mimicking depolarization with a high-K(+) solution suppressed LPS-induced TNF-α release and galectin-3 upregulation. Both depolarizing treatments with 4α-PDD and high-K(+) solution decreased store-operated Ca(2+) influx caused by thapsigargin. These results suggest that depolarization in response to opening of the TRPV4 channel attenuates the driving force for extracellular Ca(2+) and suppresses microglial activation.
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Department of Neurology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.
Dementia is one of the most debilitating symptoms of Parkinson's disease. A recent longitudinal study suggests that up to 80% of patients with Parkinson's disease will eventually develop dementia. Despite its clinical importance, the development of dementia is still difficult to predict at early stages. We previously identified olfactory dysfunction as one of the most important indicators of cortical hypometabolism in Parkinson's disease. In this study, we investigated the possible associations between olfactory dysfunction and the risk of developing dementia within a 3-year observation period. Forty-four patients with Parkinson's disease without dementia underwent the odour stick identification test for Japanese, memory and visuoperceptual assessments,(18)F-fluorodeoxyglucose positron emission tomography scans and magnetic resonance imaging scans at baseline and 3 years later. A subgroup of patients with Parkinson's disease who exhibited severe hyposmia at baseline showed more pronounced cognitive decline at the follow-up survey. By the end of the study, 10 of 44 patients with Parkinson's disease had developed dementia, all of whom had severe hyposmia at baseline. The multivariate logistic analysis identified severe hyposmia and visuoperceptual impairment as independent risk factors for subsequent dementia within 3 years. The patients with severe hyposmia had an 18.7-fold increase in their risk of dementia for each 1 SD (2.8) decrease in the score of odour stick identification test for Japanese. We also found an association between severe hyposmia and a characteristic distribution of cerebral metabolic decline, which was identical to that of dementia associated with Parkinson's disease. Furthermore, volumetric magnetic resonance imaging analyses demonstrated close relationships between olfactory dysfunction and the atrophy of focal brain structures, including the amygdala and other limbic structures. Together, our findings suggest that brain regions related to olfactory function are closely associated with cognitive decline and that severe hyposmia is a prominent clinical feature that predicts the subsequent development of Parkinson's disease dementia.
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[My paper] A Adare, S Afanasiev, C Aidala, N N Ajitanand, Y Akiba, H Al-Bataineh, J Alexander, K Aoki, Y Aramaki, E T Atomssa, R Averbeck, T C Awes, B Azmoun, V Babintsev, M Bai, G Baksay, L Baksay, K N Barish, B Bassalleck, A T Basye, S Bathe, V Baublis, C Baumann, A Bazilevsky, S Belikov, R Belmont, R Bennett, A Berdnikov, Y Berdnikov, A A Bickley, J S Bok, K Boyle, M L Brooks, H Buesching, V Bumazhnov, G Bunce, S Butsyk, C M Camacho, S Campbell, C-H Chen, C Y Chi, M Chiu, I J Choi, R K Choudhury, P Christiansen, T Chujo, P Chung, O Chvala, V Cianciolo, Z Citron, B A Cole, M Connors, P Constantin, M Csanád, T Csörgő, T Dahms, S Dairaku, I Danchev, K Das, A Datta, G David, A Denisov, A Deshpande, E J Desmond, O Dietzsch, A Dion, M Donadelli, O Drapier, A Drees, K A Drees, J M Durham, A Durum, D Dutta, S Edwards, Y V Efremenko, F Ellinghaus, T Engelmore, A Enokizono, H En'yo, S Esumi, B Fadem, D E Fields, M Finger, M Finger Jr, F Fleuret, S L Fokin, Z Fraenkel, J E Frantz, A Franz, A D Frawley, K Fujiwara, Y Fukao, T Fusayasu, I Garishvili, A Glenn, H Gong, M Gonin, Y Goto, R Granier de Cassagnac, N Grau, S V Greene, M Grosse Perdekamp, T Gunji, H-Å Gustafsson, J S Haggerty, K I Hahn, H Hamagaki, J Hamblen, R Han, J Hanks, E P Hartouni, E Haslum, R Hayano, X He, M Heffner, T K Hemmick, T Hester, J C Hill, M Hohlmann, W Holzmann, K Homma, B Hong, T Horaguchi, D Hornback, S Huang, T Ichihara, R Ichimiya, J Ide, Y Ikeda, K Imai, M Inaba, D Isenhower, M Ishihara, T Isobe, M Issah, A Isupov, D Ivanischev, B V Jacak, J Jia, J Jin, B M Johnson, K S Joo, D Jouan, D S Jumper, F Kajihara, S Kametani, N Kamihara, J Kamin, J H Kang, J Kapustinsky, K Karatsu, D Kawall, M Kawashima, A V Kazantsev, T Kempel, A Khanzadeev, K M Kijima, B I Kim, D H Kim, D J Kim, E Kim, E J Kim, S H Kim, Y J Kim, E Kinney, K Kiriluk, A Kiss, E Kistenev, L Kochenda, B Komkov, M Konno, J Koster, D Kotchetkov, A Kozlov, A Král, A Kravitz, G J Kunde, K Kurita, M Kurosawa, Y Kwon, G S Kyle, R Lacey, Y S Lai, J G Lajoie, A Lebedev, D M Lee, J Lee, K Lee, K B Lee, K S Lee, M J Leitch, M A L Leite, E Leitner, B Lenzi, X Li, P Liebing, L A Linden Levy, T Liška, A Litvinenko, H Liu, M X Liu, B Love, R Luechtenborg, D Lynch, C F Maguire, Y I Makdisi, A Malakhov, M D Malik, V I Manko, E Mannel, Y Mao, H Masui, F Matathias, M McCumber, P L McGaughey, N Means, B Meredith, Y Miake, A C Mignerey, P Mikeš, K Miki, A Milov, M Mishra, J T Mitchell, A K Mohanty, Y Morino, A Morreale, D P Morrison, T V Moukhanova, J Murata, S Nagamiya, J L Nagle, M Naglis, M I Nagy, I Nakagawa, Y Nakamiya, T Nakamura, K Nakano, J Newby, M Nguyen, R Nouicer, A S Nyanin, E O'Brien, S X Oda, C A Ogilvie, M Oka, K Okada, Y Onuki, A Oskarsson, M Ouchida, K Ozawa, R Pak, V Pantuev, V Papavassiliou, I H Park, J Park, S K Park, W J Park, S F Pate, H Pei, J-C Peng, H Pereira, V Peresedov, D Yu Peressounko, C Pinkenburg, R P Pisani, M Proissl, M L Purschke, A K Purwar, H Qu, J Rak, A Rakotozafindrabe, I Ravinovich, K F Read, K Reygers, V Riabov, Y Riabov, E Richardson, D Roach, G Roche, S D Rolnick, M Rosati, C A Rosen, S S E Rosendahl, P Rosnet, P Rukoyatkin, P Ružička, B Sahlmueller, N Saito, T Sakaguchi, K Sakashita, V Samsonov, S Sano, T Sato, S Sawada, K Sedgwick, J Seele, R Seidl, A Yu Semenov, R Seto, D Sharma, I Shein, T-A Shibata, K Shigaki, M Shimomura, K Shoji, P Shukla, A Sickles, C L Silva, D Silvermyr, C Silvestre, K S Sim, B K Singh, C P Singh, V Singh, M Slunečka, R A Soltz, W E Sondheim, S P Sorensen, I V Sourikova, N A Sparks, P W Stankus, E Stenlund, S P Stoll, T Sugitate, A Sukhanov, J Sziklai, E M Takagui, A Taketani, R Tanabe, Y Tanaka, K Tanida, M J Tannenbaum, S Tarafdar, A Taranenko, P Tarján, H Themann, T L Thomas, M Togawa, A Toia, L Tomášek, H Torii, R S Towell, I Tserruya, Y Tsuchimoto, C Vale, H Valle, H W van Hecke, E Vazquez-Zambrano, A Veicht, J Velkovska, R Vértesi, A A Vinogradov, M Virius, V Vrba, E Vznuzdaev, X R Wang, D Watanabe, K Watanabe, Y Watanabe, F Wei, R Wei, J Wessels, S N White, D Winter, J P Wood, C L Woody, R M Wright, M Wysocki, W Xie, Y L Yamaguchi, K Yamaura, R Yang, A Yanovich, J Ying, S Yokkaichi, Z You, G R Young, I Younus, I E Yushmanov, W A Zajc, C Zhang, S Zhou, L Zolin
University of Colorado, Boulder, Colorado 80309, USA.
Flow coefficients v_{n} for n=2, 3, 4, characterizing the anisotropic collective flow in Au+Au collisions at sqrt[s_{NN}]=200  GeV, are measured relative to event planes Ψ_{n}, determined at large rapidity. We report v_{n} as a function of transverse momentum and collision centrality, and study the correlations among the event planes of different order n. The v_{n} are well described by hydrodynamic models which employ a Glauber Monte Carlo initial state geometry with fluctuations, providing additional constraining power on the interplay between initial conditions and the effects of viscosity as the system evolves. This new constraint can serve to improve the precision of the extracted shear viscosity to entropy density ratio η/s.
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Division of Neurology, Department of Neuroscience & Sensory Organs, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
MANY NEURODEGENERATIVE DISEASES SHARE A COMMON PATHOLOGICAL FEATURE: the deposition of amyloid-like fibrils composed of misfolded proteins. Emerging evidence suggests that these proteins may spread from cell-to-cell and encourage the propagation of neurodegeneration in a prion-like manner. Here, we demonstrated that α-synuclein (αSYN), a principal culprit for Lewy pathology in Parkinson's disease (PD), was present in endosomal compartments and detectably secreted into the extracellular milieu. Unlike prion protein, extracellular αSYN was mainly recovered in the supernatant fraction rather than in exosome-containing pellets from the neuronal culture medium and cerebrospinal fluid. Surprisingly, impaired biogenesis of multivesicular body (MVB), an organelle from which exosomes are derived, by dominant-negative mutant vacuolar protein sorting 4 (VPS4) not only interfered with lysosomal targeting of αSYN but facilitated αSYN secretion. The hypersecretion of αSYN in VPS4-defective cells was efficiently restored by the functional disruption of recycling endosome regulator Rab11a. Furthermore, both brainstem and cortical Lewy bodies in PD were found to be immunoreactive for VPS4. Thus, VPS4, a master regulator of MVB sorting, may serve as a determinant of lysosomal targeting or extracellular secretion of αSYN and thereby contribute to the intercellular propagation of Lewy pathology in PD.
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Department of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8501, Japan.
Store-operated channels (SOC) are Ca(2+)-permeable channels that are activated by IP(3)-receptor-mediated Ca(2+) depletion of the endoplasmic reticulum (ER). Recent studies identify a membrane pore subunits, Orai1 and a Ca(2+) sensor on ER, STIM1 as components of Ca(2+) release-activated Ca(2+)(CRAC) channels, which are well-characterized SOCs. On the other hand, proteins that act as modulators of SOC activity remain to be identified. Calumin is a Ca(2+)-binding protein that resides on the ER and functional experiments using calumin-null mice demonstrate that it is involved in SOC function, although its role is unknown. This study used electrophysiological analysis to explore whether calumin modulates CRAC channel activity. CRAC channel currents were absent in HEK293 cells co-expressing calumin with the CRAC channel components, Orai1 or STIM1. Meanwhile, HEK cells that co-expressed calumin with CRAC channels exhibited larger currents with slower inactivation than cells expressing CRAC channels alone. The current-voltage relationship showed an inwardly rectifying current, but a negative shift in the reversal potential of greater than 60mV was observed in HEK cells co-expressing calumin with CRAC channels. In addition, the permeability coefficient ratio of Ca(2+) over monovalent cations was much lower than that of cells expressing CRAC channels alone. Replacement of Na(+) with N-methyl-d-glucamine(+) in the external solution noticeably diminished the CRAC current in HEK cells co-expressing calumin and CRAC channels. In a Cs(+)-based external solution, CRAC current was not observed in either cell-type. In addition, Ca(2+) imaging analysis revealed that co-transfection of calumin reduced extracellular Ca(2+) influx via CRAC channels. Further, calumin was shown to be directly associated with CRAC channels. These results reveal a novel mechanism for the regulation of CRAC channels by calumin.
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Department of Morphological Brain Science, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan, Japan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST), Tokyo 102-0075, Japan, and Department of Anatomy for Oral Sciences, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
Corticothalamic projection neurons in the cerebral cortex constitute an important component of the thalamocortical reciprocal circuit, an essential input/output organization for cortical information processing. However, the spatial organization of local excitatory connections to corticothalamic neurons is only partially understood. In the present study, we first developed an adenovirus vector expressing somatodendritic membrane-targeted green fluorescent protein. After injection of the adenovirus vector into the ventrobasal thalamic complex, a band of layer (L) 6 corticothalamic neurons in the rat barrel cortex were retrogradely labeled. In addition to their cell bodies, fine dendritic spines of corticothalamic neurons were well visualized without the labeling of their axon collaterals or thalamocortical axons. In cortical slices containing retrogradely labeled L6 corticothalamic neurons, we intracellularly stained single pyramidal/spiny neurons of L2-6. We examined the spatial distribution of contact sites between the local axon collaterals of each pyramidal neuron and the dendrites of corticothalamic neurons. We found that corticothalamic neurons received strong and focused connections from L4 neurons just above them, and that the most numerous nearby and distant sources of local excitatory connections to corticothalamic neurons were corticothalamic neurons themselves and L6 putative corticocortical neurons, respectively. These results suggest that L4 neurons may serve as an important source of local excitatory inputs in shaping the cortical modulation of thalamic activity.
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Department of Chemical Engineering, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki-aza Aoba-ku, Sendai, 980-8579, Japan.
Hollow silica particle was obtained with a vesicle template synthesis in water under ambient conditions in the presence of ammonia. Biomimetic vesicles, liposomes were used, which consisted of a zwitterionic phospholipid, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and a tiny amount of charged amphiphiles, hexadecylamine (HDA) or dicetylphosphate (DCP). Aggregation of silica occurred for DPPC or cationic DPPC/HDA liposome, whereas well-dispersed hollow silica particle could be obtained for anionic DPPC/DCP liposome. The hollow particle synthesized with the anionic liposome had single-layered and raspberry-like structures. Electrostatic repulsion between anionic vesicles maintained stable dispersion of the as-synthesized particles during the reaction. Formation of the raspberry-like morphology is explained by silica particle precipitation selectively induced around the liposomes under basic conditions due to affinity of silica precursors for the liposomes. Synthesis of well-dispersed hollow silica particle with a raspberry-like morphology is the first report in vesicle template syntheses.
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2012-05-22 17:24:44 © BioInfoBank Institute