Neutron-capture elements in the very metal-poor star HD88609: another st ar with excesses of light neutron-capture elements

We obtained a high resolution, high signal-to-noise UV-blue spectrum of the extremely metal-poor red giant HD88609 to determine the abundances of heavy elements. Nineteen neutron-capture elements are detected in the spectrum. Our analysis revealed that this object has large excesses of light neutron-capture elements while heavy neutron-capture elements are deficient. The abundance pattern shows a continuously decreasing trend, as a function of atomic number, from Sr to Yb, which is quite different from those in stars with excesses of r-process elements. Such an abundance pattern is very similar to that of HD122563 that was studied by our previous work. The results indicate that the abundance pattern found in the two stars could represent the pattern produced by the nucleosynthesis process that provided light neutron-capture elements in the very early Galaxy.Comment: 18 pages, 6 figures, accepted for publication in Ap

Live-cell imaging to analyze intracellular aggregation of recombinant IgG in CHO cells

Recombinant immunoglobulin G (IgG) aggregates are formed during their production. However, the process underlying intracellular/extracellular aggregation in cell culture conditions is not well understood, and no effective method exists to assess IgG aggregates. Here, we establish an approach to detect intracellular aggregates using AF.2A1, a small artificial protein that binds to non-native IgG conformers and aggregates. Fluorescent-labeled AF.2A1 is prepared via conjugation and transfected into antibody-producing Chinese hamster ovary (CHO) cells. Micrographic images show intracellular IgG aggregates in CHO cells. The relative amount of intracellular aggregates (versus total intracellular IgG) differed depending on the type of additives used during cell culture. Interestingly, the relative amount of intracellular aggregates moderately correlates with that of in vitro extracellular IgG aggregates, suggesting they are secreted. This method will allow the investigation of antibody aggregation in cells, and may guide the production of therapeutic antibodies with high yield/quality

小規模マイコンによるIoT機器向けパーティショニングフレームワークの実現

2020南山大学小規模マイコンによるIoT機器向けパーティショニングフレームワークの実現2017～2020年度科学研究費助成事業 (基盤研究 (C) (一般)) 研究成果報告

Molecular Mechanism Underlying the Suppression of CPB2 Expression Caused by Persistent Hepatitis C Virus RNA Replication

The mechanisms of hepatitis C virus (HCV)-associated hepatocarcinogenesis and disease progression are unclear. We previously observed that the expression level of carboxypeptidase B2 (CPB2) gene was remarkably suppressed by persistent HCV RNA replication in human hepatoma cell line Li23-derived cells. The results of the present study demonstrated that the CPB2 expression in patients with chronic hepatitis C was inversely correlated with several risk factors of hepatic fibrosis or steatosis, although ectopic CPB2 expression did not suppress the expression of fibrogenic or lipogenic genes. The suppressed CPB2 expression was restored by treatment with 5-azacytidine. To clarify the mechanism underlying this phenomenon, we analyzed the CPB2 promoter, and the results revealed that (1) hepatocyte nuclear factor 1 (HNF1), especially HNF1α, was essential for the CPB2 promoter, and (2) CPB2 promoter was not methylated by persistent HCV RNA replication. The expression levels of HNF1α and HNF1β were also not changed by persistent HCV RNA replication. These results suggest the existence of 5-azacytidine-inducible or -reducible unknown factor(s) that can control the CPB2 expression. To evaluate this idea we performed a microarray analysis, and several gene candidates corresponding to the suggested factor(s) were identified

Photo-isolation chemistry for high-resolution and deep spatial transcriptome with mouse tissue sections

Photo-isolation chemistry (PIC) enables isolation of transcriptome information from locally defined areas by photo-irradiation. Here, we present an optimized PIC protocol for formalin-fixed frozen and paraffin mouse sections and fresh-frozen mouse sections. We describe tissue section preparation and permeabilization, followed by in situ reverse transcription using photo-caged primers. We then detail immunostaining and UV-mediated uncaging to the target areas, followed by linear amplification of uncaged cDNAs, library preparation, and quantification. This protocol can be applied to various animal tissue types

Western North Pacific Integrated Physical-Biogeochemical Ocean Observation Experiment (INBOX): Part 2. Biogeochemical responses to eddies and typhoons revealed from the S1 mooring and shipboard measurements

An interdisciplinary project called S1-INBOX (Western North Pacific Integrated PhysicalBiogeochemical Ocean Observation Experiment conducted around the S1 biogeochemical mooring site) was carried out during the summer of 2011 in the oligotrophic, subtropical North Pacific Ocean near biogeochemical mooring S1 (30° N, 145° E). Results from the S1 mooring during S1-INBOX revealed a large export flux at a depth of 200 m, a high chlorophyll a concentration in the deep chlorophyll maximum layer, and a high potential photochemical efficiency of photosystem II. These phenomena were associated with vertical uplift of isopycnal surfaces at the edge of a cyclonic eddy and a transition from the cyclonic eddy to an anticyclonic eddy. Shipboard biogeochemical surveys conducted during oligotrophic conditions in July 2011 revealed that the phytoplankton community in these waters was dominated by small species that are responsive to intermittent supplies of nutrients. Surface wind forcing because of Typhoons MA-ON and SONCA may have generated near-inertial oscillations. Diapycnal mixing associated with near-inertial waves was also related to high export fluxes, the indication being that propagation of near-inertial internal waves and subsequent mixing may have been important to biogeochemical phenomena during S1-INBOX