京都大学 · 材料科学
Takashi Nozawa教授の研究室では、心筋の力学的・エネルギー的特性と細胞内シグナル伝達の両面から循環器系の機能を解明しています。特に心室の圧-容量関係とエネルギー効率の関係を動物モデルを用いて解析しており、心不全のメカニズム解明に貢献しています。また、細菌感染における細胞自食体の制御機構についても、GAS感染をモデルとして分子メカニズムを解明しています。
Figures are computed from collected data and may differ slightly.
We studied the effects of ventricular end-systolic elastance (Ees) and effective arterial elastance (Ea) on the efficiency of energy transfer from pressure-volume area (PVA) to external mechanical work (EW) in the left ventricle of anesthetized closed-chest dogs. PVA represents the total mechanical energy generated by ventricular contraction, which is an intermediate form of energy between oxygen consumption, the total energy input, and EW, the effective energy output. PVA and EW were determined
Streptococcus pyogenes, one of the major human pathogens, is a unique species since it has acquired diverse strain-specific virulence properties mainly through the acquisition of streptococcal prophages. In addition, S. pyogenes possesses clustered regularly interspaced short palindromic repeats (CRISPR)/Cas systems that can restrict horizontal gene transfer (HGT) including phage insertion. Therefore, it was of interest to examine the relationship between CRISPR and acquisition of prophages in S
The relationship between the total loss under tensile stress and the tilt angle of the [001] out of crystal surface β was studied in 3 percent Si-Fe single crystals. The total loss largely depends upon β. When β is about 2°, the total loss under tensile stress is the smallest, and the decrease of the total loss due to tensile stress is the largest. When β is less than about 2°, the total loss increases as β decreases. In the case of perfect
Autophagy mediates the degradation of cytoplasmic contents in the lysosome and plays a significant role in immunity. Here we identified the small GTPases Rab9A and Rab23 as novel autophagy regulators during Group A streptococcus (GAS) infection. Rab9A was recruited to GAS-containing autophagosome-like vacuoles (GcAVs) after autophagosomal maturation and its activity was required for GcAV enlargement and eventual lysosomal fusion. GcAV enlargement appeared to be related to homotypic fusion of GcA
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