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방향족 폴리우레탄의 합성과 수소결합 상호작용에 의한 액정성의 발견
Uryu, Toshiyuki,이종백 한국공업화학회 1998 응용화학 Vol.2 No.2
Thermotropic polymers consisting of mesogenic units in the main chain have attracted attention for the demand of high performance materials. We reported that polyurethanes obtained by polyaddition of 1,4-phenylene diisocyanate or 2,5-tolylene diisocyanate, with 1,4-bis(w-hydroxyalkoxy)benzene showed monotropic liquid crystalline behaviors. In the present study, thermotropic properties of liquid crystalline polyurethanes have been investigigated by wide-angle x-ray scattering and infrared spectroscopy. Curve-fitting analysis of the C=O band region of infrared spectra at various temperatures revealed three bands the ordered H-bonded carbonyl band the disordered H-bonded carbonyl band, and the free carbonyl band. The mesomorphic behavior of the polyurethanes was greatly dependent on the hydrogen bonds between the urethane linkage.
Spacer 의 변화에 의한 Thermotropic Polyamide 및 Copolyamide 의 합성
송진철,김경환,Toshiyuki Uryu 한국염색가공학회 1993 韓國染色加工學會誌 Vol.5 No.2
Synthesis and liquid-crystallinites of thermotropic polyamides and copolyamides were investigated. Thermotropic polyamides and copolyamides containing a flexible spacer in the backbone were obtained by the two or three components melt polycondensations of 4,4'-dicarboxy-${\alpha}$${\omega}$-diphenoxy alkane as an A components, 4,4'-diacetoamido-3,3' dimethoxybiphenyl as a B, 1,4-diacetoamido-benzene (diacetylated p-phenylenediamine) was used as another amide-group-forming minomer. The content of the amide groups in the thermotropic polyamide and Copolyamide widely varied depending on the structure of the amide-group forming diacetoamido monomers. A polymer (9CLDI) showed a typical nematic texture between 218$^{circle}C$ ($T_m$) and 345$^{circle}C$($T_i$) The melting points of the members of this series of polymers increased with decreasing methylene spacer. The polymer structure and mesmorphic nature were examined by solid and solution ${^13}C$-NMR spectroscopy, cross polarizing microscopy with a hot stage.
( Takeshi Hashimoto ),( Yoko Okada ),( Atsushi Yamanaka ),( Natsuhiko Ono ),( Keisuke Uryu ),( Isafumi Maru ) 한국운동영양학회 2020 Physical Activity and Nutrition (Phys Act Nutr) Vol.24 No.3
[Purpose] In vivo studies have demonstrated the ergogenic benefits of eleutherococcus senticosus (ES) supplementation. ES has been observed to enhance endurance capacity, improve cardiovascular function, and alter metabolic functions (e.g., increased fat utilization); however, the exact mechanisms involved remain unknown. We aimed to determine whether ES could effectively induce fat loss and improve muscle metabolic profiles through increases in lipolysis- and lipid metabolism-associated protein expression in 3T3-L1 adipocytes and C2C12 skeletal muscle cells, respectively, to uncover the direct effects of ES on adipocytes and skeletal muscle cells. [Methods] Different doses of ES extracts (0.2, 0.5, and 1.0 mg/mL) were added to cells (0.2 ES, 0.5 ES, and 1.0 ES, respectively) for 72 h and compared to the vehicle control (control). [Results] The intracellular triacylglycerol (TG) content significantly decreased (p < 0.05 for 0.2 ES, p < 0.01 for 0.5 ES and 1.0 ES) in 3T3-L1 cells. Adipose triglyceride lipase, which is involved in active lipolysis, was significantly higher in the 1.0 ES group than in the control group (p < 0.01) of 3T3-L1 adipocytes. In C2C12 cells, the mitochondrial protein voltage-dependent anion channel (VDAC) was significantly increased in the 1.0 ES group (p < 0.01). Furthermore, we found that 1.0 ES activated both 5' AMP-activated protein kinase (AMPK) and acetyl-CoA carboxylase (ACC) in skeletal muscle cells (p < 0.01). [Conclusion] These findings suggest that ES extracts decreased TG content, presumably by increasing lipase in adipocytes and metabolism-associated protein expression as well as mitochondrial biogenesis in muscle cells. These effects may corroborate previous in vivo findings regarding the ergogenic effects of ES supplementation.
VEGF-Induced Vascular Permeability Is Mediated by FAK
Chen, X.,Nam, J.O.,Jean, C.,Lawson, C.,Walsh, Colin T.,Goka, E.,Lim, S.T.,Tomar, A.,Tancioni, I.,Uryu, S.,Guan, J.L.,Acevedo, Lisette M.,Weis, Sara M.,Cheresh, David A.,Schlaepfer, David D. Cell Press 2012 DEVELOPMENTAL CELL Vol.22 No.1
Endothelial cells (ECs) form cell-cell adhesive junctional structures maintaining vascular integrity. This barrier is dynamically regulated by vascular endothelial growth factor (VEGF) receptor signaling. We created an inducible knockin mouse model to study the contribution of the integrin-associated focal adhesion tyrosine kinase (FAK) signaling on vascular function. Here we show that genetic or pharmacological FAK inhibition in ECs prevents VEGF-stimulated permeability downstream of VEGF receptor or Src tyrosine kinase activation in vivo. VEGF promotes tension-independent FAK activation, rapid FAK localization to cell-cell junctions, binding of the FAK FERM domain to the vascular endothelial cadherin (VE-cadherin) cytoplasmic tail, and direct FAK phosphorylation of β-catenin at tyrosine-142 (Y142) facilitating VE-cadherin-β-catenin dissociation and EC junctional breakdown. Kinase inhibited FAK is in a closed conformation that prevents VE-cadherin association and limits VEGF-stimulated β-catenin Y142 phosphorylation. Our studies establish a role for FAK as an essential signaling switch within ECs regulating adherens junction dynamics.