Structural Transitions and Magnetic Structure in NH4CuCl3 via 14N-NMR

We report results of 14N-NMR experiments on NH4CuCl3 at the magnetic field of 7 T, where the 1/4-magnetization plateau is observed at low temperatures. The quadrupole splitting parameter $\nu_{z}$ splits below 70 K, indicating a structural phase transition. At 4.2 K, eight N sites with distinct values of both $\nu_{z}$ and the magnetic hyperfine shift $K_{z}$ are resolved in the NMR spectrum for general field directions. We then conlude that the magnetic structure in the 1/4-plateau does not break the symmetry of the crystal. Based on the NMR and the recent neutron scattering results by Ruegg et al. [Phys. Rev. Lett. 93 (2004) 037207], we propose that triplet dimers in the 1/4-plateau is formed not between the nearest neighbor pairs but over different chains.Comment: 7 pages, 5 figures, Proceedings for the International Symposium on Quantum Spin Systems, submitted to Prog. Theor. Phys. Author chang

The Interaction of LFA-1 on Mononuclear Cells and ICAM-1 on Tubular Epithelial Cells Accelerates TGF-β1-Induced Renal Epithelial-Mesenchymal Transition

The epithelial-mesenchymal transition (EMT) of renal epithelial cells (RTECs) has pivotal roles in the development of renal fibrosis. Although the interaction of lymphocyte function-associated antigen 1 (LFA-1) on leukocytes and its ligand, intracellular adhesion molecule 1 (ICAM-1), plays essential roles in most inflammatory reactions, its pathogenetic role in the EMT of RTECs remains to be clarified. In the present study, we investigated the effect of the interaction of LFA-1 on peripheral blood mononuclear cells (PBMCs) and ICAM-1 on HK-2 cells after stimulation with TGF-β1 on the EMT of RTECs. ICAM-1 was highly expressed in HK-2 cells. After TGF-β1 stimulation, the chemokines CCL3 and CXCL12 increased on HK-2 cells. After co-culture of PBMCs and HK-2 cells pre-stimulated with TGF-β1 (0.1 ng/ml) (HK-2-TGF-β1 (0.1)), the expression of the active form of LFA-1 increased on PBMCs; however, total LFA-1 expression did not change. The expression of the active form of LFA-1 on PBMCs did not increase after co-culture with not CCL3 but CXCL12 knockdown HK-2-TGF-β1 (0.1). The expression of epithelial cell junction markers (E-cadherin and occludin) further decreased and that of mesenchymal markers (vimentin and fibronectin) further increased in HK-2-TGF-β1 (0.1) after co-culture with PBMCs for 24 hrs (HK-2-TGF-β1 (0.1)-PBMCs). The phosphorylation of ERK 1/2 but not smad2 and smad3 increased in HK-2-TGF-β1 (0.1)-PBMCs. The snail and slug signaling did not increase HK-2-TGF-β1 (0.1)-PBMCs. Although the migration and invasion of HK-2 cells induced full EMT by a high dose (10.0 ng/ml) and long-term (72–96 hrs) TGF-β1 stimulation increased, that of HK-2-TGF-β1 (0.1)-PBMCs did not increase. These results suggested that HK-2 cells stimulated with TGF-β1 induced conformational activation of LFA-1 on PBMCs by increased CXCL12. Then, the direct interaction of LFA-1 on PBMCs and ICAM-1 on HK-2 cells activated ERK1/2 signaling to accelerate the part of EMT of HK-2 cells induced by TGF-β1

NH4CuCl3 ニ オケル ジカ プラトー ノ 15N-NMR オ モチイタ ビシテキ シテン カラノ ケンキュウ

京都大学0048新制・課程博士博士(人間・環境学)甲第11118号人博第257号16||148(吉田南総合図書館)新制||人||65(附属図書館)22668UT51-2004-L915京都大学大学院人間・環境学研究科文化・地域環境学専攻(主査)教授 前川 覚, 教授 冨田 博之, 助教授 藤原 直樹学位規則第4条第1項該当Doctor of Human and Environmental StudiesKyoto UniversityDA