Spatial contexts can inhibit a mislocalization of visual stimuli during smooth pursuit

The position of a flash presented during pursuit is mislocalized in the direction of the pursuit. Although this has been explained by a temporal mismatch between the slow visual processing of flash and fast efferent signals on eye positions, here we show that spatial contexts also play an important role in determining the flash position. We put various continuously lit objects (walls) between veridical and to-be-mislocalized positions of flash. Consequently, these walls significantly reduced the mislocalization of flash, preventing the flash from being mislocalized beyond the wall (Experiment 1). When the wall was shortened or had a hole in its center, the shape of the mislocalized flash was vertically shortened as if cutoff or funneled by the wall (Experiment 2). The wall also induced color interactions; a red wall made a green flash appear yellowish if it was in the path of mislocalization (Experiment 3). Finally, those flash–wall interactions could be induced even when the walls were presented after the disappearance of flash (Experiment 4). These results indicate that various features (position, shape, and color) of flash during pursuit are determined with an integration window that is spatially and temporally broad, providing a new insight for generating mechanisms of eye-movement mislocalizations

A Variety of Ag-O Bonding Modes and Antimicrobial Activities of Light-Stable Coinage Metal Complexes with Carboxylate Ligands

Using light-stable dimeric silver(I) carboxylate precursors {[Ag(Hpyrrld)]_2}_n formed with chiral and racemic forms of 2-pyrrolidone-5-carboxylic acid (H_2pyrrld) ligand, six novel light-stable, triphenylphosphinesilver(I) complexes consisting of both a hard Lewis base (O atom) and a soft Lewis base (P atom) were prepared, i.e. [Ag_2(R-Hpyrrld)_2(H_2O)(PPh_3)_2]・H_2O 1,[Ag(R-Hpyrrld)(PPh_3)_2]_2 2, [Ag_2(S-Hpyrrld)_2(H_2O)(PPh_3)_2]・H_2O 3, [Ag(S-Hpyrrld)(PPh_3)_2]_2 4,{[Ag(R,S-Hpyrrld)(PPh_3)]_2}_n 5 and [Ag(R,S-Hpyrrld)(PPh_3)_2] 6. Their solid-state and solution structures were unequivocally characterized with elemental analysis, TG/DTA, FTIR, X-ray structure analysis, molecular weight measurements in EtOH with the vaporimetric method, solution (^1H, ^C, ^P) NMR and solid-state ^P CPMAS NMR spectroscopy. Two sets of enantiomeric complexes were isolated as (1 and 3) and (2 and 4). X-ray crystallography revealed that these complexes possessed different Ag-O bonding modes, depending on the number of PPh_3 ligands and the chirality of the Hpyrrld ligand. Complexes 1-6 behaved as a monomeric species in EtOH and CD_2Cl_2. Antimicrobial activites by silver(I) complexes in the water-suspension system against selected bacteria, yeast and molds were significantly correlated with the number of coordinating PPh_3 ligands per silver(I) atom in the complexes

Current Performance and On-Going Improvements of the 8.2 m Subaru Telescope

An overview of the current status of the 8.2 m Subaru Telescope constructed and operated at Mauna Kea, Hawaii, by the National Astronomical Observatory of Japan is presented. The basic design concept and the verified performance of the telescope system are described. Also given are the status of the instrument package offered to the astronomical community, the status of operation, and some of the future plans. The status of the telescope reported in a number of SPIE papers as of the summer of 2002 are incorporated with some updates included as of 2004 February. However, readers are encouraged to check the most updated status of the telescope through the home page, http://subarutelescope.org/index.html, and/or the direct contact with the observatory staff.Comment: 18 pages (17 pages in published version), 29 figures (GIF format), This is the version before the galley proo

Differential orientation effect in the neural response to interacting biological motion of two agents

<p>Abstract</p> <p>Background</p> <p>A recent behavioral study demonstrated that the meaningful interaction of two agents enhances the detection sensitivity of biological motion (BM), however, it remains unclear when and how the 'interaction' information of two agents is represented in our neural system. To clarify this point, we used magnetoencephalography and introduced a novel experimental technique to extract a neuromagnetic response relating to two-agent BM perception. We then investigated how this response was modulated by the interaction of two agents. In the present experiment, we presented two kinds of visual stimuli (interacting and non-interacting BM) with two orientations (upright and inverted).</p> <p>Results</p> <p>We found a neuromagnetic response in the bilateral occipitotemporal region, on average 300 – 400 ms after the onset of a two-agent BM stimulus. This result showed that interhemispheric differences were apparent for the peak amplitudes. For the left hemisphere, the orientation effect was manifest when the two agents were made to interact, and the interaction effect was manifest when the stimulus was inverted. In the right hemisphere, the main effects of both orientation and interaction were significant, suggesting that the peak amplitude was attenuated when the visual stimulus was inverted or made to interact.</p> <p>Conclusion</p> <p>These results demonstrate that the 'interaction' information of two agents can affect the neural activities in the bilateral occipitotemporal region, on average 300 – 400 ms after the onset of a two-agent BM stimulus, however, the modulation was different between hemispheres: the left hemisphere is more concerned with dynamics, whereas the right hemisphere is more concerned with form information.</p

The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force

「コロナ制圧タスクフォース」COVID-19患者由来の血液細胞における遺伝子発現の網羅的解析 --重症度に応じた遺伝子発現の変化には、ヒトゲノム配列の個人差が影響する--. 京都大学プレスリリース. 2022-08-23.Coronavirus disease 2019 (COVID-19) is a recently-emerged infectious disease that has caused millions of deaths, where comprehensive understanding of disease mechanisms is still unestablished. In particular, studies of gene expression dynamics and regulation landscape in COVID-19 infected individuals are limited. Here, we report on a thorough analysis of whole blood RNA-seq data from 465 genotyped samples from the Japan COVID-19 Task Force, including 359 severe and 106 non-severe COVID-19 cases. We discover 1169 putative causal expression quantitative trait loci (eQTLs) including 34 possible colocalizations with biobank fine-mapping results of hematopoietic traits in a Japanese population, 1549 putative causal splice QTLs (sQTLs; e.g. two independent sQTLs at TOR1AIP1), as well as biologically interpretable trans-eQTL examples (e.g., REST and STING1), all fine-mapped at single variant resolution. We perform differential gene expression analysis to elucidate 198 genes with increased expression in severe COVID-19 cases and enriched for innate immune-related functions. Finally, we evaluate the limited but non-zero effect of COVID-19 phenotype on eQTL discovery, and highlight the presence of COVID-19 severity-interaction eQTLs (ieQTLs; e.g., CLEC4C and MYBL2). Our study provides a comprehensive catalog of whole blood regulatory variants in Japanese, as well as a reference for transcriptional landscapes in response to COVID-19 infection

DOCK2 is involved in the host genetics and biology of severe COVID-19

「コロナ制圧タスクフォース」COVID-19疾患感受性遺伝子DOCK2の重症化機序を解明 --アジア最大のバイオレポジトリーでCOVID-19の治療標的を発見--. 京都大学プレスリリース. 2022-08-10.Identifying the host genetic factors underlying severe COVID-19 is an emerging challenge. Here we conducted a genome-wide association study (GWAS) involving 2, 393 cases of COVID-19 in a cohort of Japanese individuals collected during the initial waves of the pandemic, with 3, 289 unaffected controls. We identified a variant on chromosome 5 at 5q35 (rs60200309-A), close to the dedicator of cytokinesis 2 gene (DOCK2), which was associated with severe COVID-19 in patients less than 65 years of age. This risk allele was prevalent in East Asian individuals but rare in Europeans, highlighting the value of genome-wide association studies in non-European populations. RNA-sequencing analysis of 473 bulk peripheral blood samples identified decreased expression of DOCK2 associated with the risk allele in these younger patients. DOCK2 expression was suppressed in patients with severe cases of COVID-19. Single-cell RNA-sequencing analysis (n = 61 individuals) identified cell-type-specific downregulation of DOCK2 and a COVID-19-specific decreasing effect of the risk allele on DOCK2 expression in non-classical monocytes. Immunohistochemistry of lung specimens from patients with severe COVID-19 pneumonia showed suppressed DOCK2 expression. Moreover, inhibition of DOCK2 function with CPYPP increased the severity of pneumonia in a Syrian hamster model of SARS-CoV-2 infection, characterized by weight loss, lung oedema, enhanced viral loads, impaired macrophage recruitment and dysregulated type I interferon responses. We conclude that DOCK2 has an important role in the host immune response to SARS-CoV-2 infection and the development of severe COVID-19, and could be further explored as a potential biomarker and/or therapeutic target