Pro-inflammatory/Th1 gene expression shift in high glucose stimulated mesangial cells and tubular epithelial cells.
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S. Kaneko | K. Matsushima | K. Yokota | S. Hashimoto | T. Wada | S. Kitajima | T. Toyama | Y. Iwata | N. Sakai | K. Furuichi | Y. Shinozaki | A. Sagara | H. Yasuda
[1] Jurong Yang,et al. ATP-P2X4 signaling mediates NLRP3 inflammasome activation: a novel pathway of diabetic nephropathy. , 2013, The international journal of biochemistry & cell biology.
[2] S. Kaneko,et al. CCL2/CCR2 augments the production of transforming growth factor-beta1, type 1 collagen and CCL2 by human CD45-/collagen 1-positive cells under high glucose concentrations , 2013, Clinical and Experimental Nephrology.
[3] J. O’Shea,et al. Helper T‐cell identity and evolution of differential transcriptomes and epigenomes , 2013, Immunological reviews.
[4] G. Ramesh,et al. Proximal tubule-specific overexpression of netrin-1 suppresses acute kidney injury-induced interstitial fibrosis and glomerulosclerosis through suppression of IL-6/STAT3 signaling. , 2013, American journal of physiology. Renal physiology.
[5] H. Makino,et al. Inflammation and the pathogenesis of diabetic nephropathy. , 2013, Clinical science.
[6] B. Kestenbaum,et al. Kidney disease and increased mortality risk in type 2 diabetes. , 2013, Journal of the American Society of Nephrology : JASN.
[7] A. Duschl,et al. STAT6-dependent and -independent mechanisms in Th2 polarization , 2012, European journal of immunology.
[8] G. Tesch,et al. Inflammation in Diabetic Nephropathy , 2012, Mediators of inflammation.
[9] S. Tang,et al. The pathogenic role of the renal proximal tubular cell in diabetic nephropathy. , 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[10] P. Greengard,et al. IRE1α induces thioredoxin-interacting protein to activate the NLRP3 inflammasome and promote programmed cell death under irremediable ER stress. , 2012, Cell metabolism.
[11] L. Morel,et al. Aberrant Macrophages Mediate Defective Kidney Repair That Triggers Nephritis in Lupus-Susceptible Mice , 2012, The Journal of Immunology.
[12] Alberto Mantovani,et al. Macrophage plasticity and polarization: in vivo veritas. , 2012, The Journal of clinical investigation.
[13] J. Moon,et al. Aberrant Recruitment and Activation of T Cells in Diabetic Nephropathy , 2012, American Journal of Nephrology.
[14] S. Holdsworth,et al. Signal transducer and activation of transcription 6 (STAT6) regulates T helper type 1 (Th1) and Th17 nephritogenic immunity in experimental crescentic glomerulonephritis , 2011, Clinical and experimental immunology.
[15] Yuh-Feng Lin,et al. Role of T Cells in Type 2 Diabetic Nephropathy , 2011, Experimental diabetes research.
[16] W. Patsch,et al. Potential Role of Regulatory T Cells in Reversing Obesity-Linked Insulin Resistance and Diabetic Nephropathy , 2011, Diabetes.
[17] D. Scott,et al. Activation of Protein Kinase C-ζ in Pancreatic β-Cells In Vivo Improves Glucose Tolerance and Induces β-Cell Expansion via mTOR Activation , 2011, Diabetes.
[18] D. Harris,et al. IL-25 induces M2 macrophages and reduces renal injury in proteinuric kidney disease. , 2011, Journal of the American Society of Nephrology : JASN.
[19] M. Hall,et al. mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in mice. , 2011, The Journal of clinical investigation.
[20] L. Gesualdo,et al. IL‐17 Expression by Tubular Epithelial Cells in Renal Transplant Recipients with Acute Antibody‐Mediated Rejection , 2011, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.
[21] F. Brosius,et al. GLUT1 enhances mTOR activity independently of TSC2 and AMPK. , 2011, American journal of physiology. Renal physiology.
[22] D. Harris,et al. Transfused Macrophages Ameliorate Pancreatic and Renal Injury in Murine Diabetes Mellitus , 2011, Nephron Experimental Nephrology.
[23] H. Bagavant,et al. Mesangial pathology in glomerular disease: targets for therapeutic intervention. , 2010, Advanced drug delivery reviews.
[24] C. Spencer,et al. Mammalian target of rapamycin protein complex 2 regulates differentiation of Th1 and Th2 cell subsets via distinct signaling pathways. , 2010, Immunity.
[25] A. Sanz,et al. Suppressors of cytokine signaling abrogate diabetic nephropathy. , 2010, Journal of the American Society of Nephrology : JASN.
[26] W. Paul,et al. Mechanisms Underlying Lineage Commitment and Plasticity of Helper CD4+ T Cells , 2010, Science.
[27] S. Twigg,et al. Mesangial cell-derived factors alter monocyte activation and function through inflammatory pathways: possible pathogenic role in diabetic nephropathy. , 2009, American journal of physiology. Renal physiology.
[28] S. Kaneko,et al. Dendritic Cells Contribute to Autoimmune Kidney Injury in MRL-Faslpr Mice , 2009, The Journal of Rheumatology.
[29] A. Breggia,et al. JAK2/Y343/STAT5 signaling axis is required for erythropoietin-mediated protection against ischemic injury in primary renal tubular epithelial cells. , 2008, American journal of physiology. Renal physiology.
[30] J. Jenkins,et al. Antiapoptotic properties of erythropoiesis-stimulating proteins in models of cisplatin-induced acute kidney injury. , 2008, American journal of physiology. Renal physiology.
[31] M. Cooper,et al. Inhibition of NADPH Oxidase Prevents Advanced Glycation End Product–Mediated Damage in Diabetic Nephropathy Through a Protein Kinase C-α–Dependent Pathway , 2008, Diabetes.
[32] S. Kaneko,et al. Reduction in Chronic Allograft Nephropathy by Inhibition of p38 Mitogen-Activated Protein Kinase , 2006, American Journal of Nephrology.
[33] N. Yorioka,et al. PDGF receptor tyrosine kinase inhibitor suppresses mesangial cell proliferation involving STAT3 activation , 2006, Clinical and experimental immunology.
[34] H. Rabb,et al. Contrasting roles for STAT4 and STAT6 signal transduction pathways in murine renal ischemia-reperfusion injury. , 2003, American journal of physiology. Renal physiology.
[35] K. Matsushima,et al. Administration of FR167653, a new anti-inflammatory compound, prevents renal ischaemia/reperfusion injury in mice. , 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[36] M. G. Koerkamp,et al. Dynamics of gene expression revealed by comparison of serial analysis of gene expression transcript profiles from yeast grown on two different carbon sources. , 1999, Molecular biology of the cell.
[37] J. Krepinsky,et al. High glucose-induced RhoA activation requires caveolae and PKCβ1-mediated ROS generation. , 2012, American journal of physiology. Renal physiology.
[38] T. Wada,et al. Involvement of extracellular signal-regulated kinase and p38 in human diabetic nephropathy. , 2005, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[39] K. Matsushima,et al. p38 Mitogen-activated protein kinase contributes to autoimmune renal injury in MRL-Fas lpr mice. , 2003, Journal of the American Society of Nephrology : JASN.