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10.3892/mmr.2016.5786 http://scihub22266oqcxt.onion/10.3892/mmr.2016.5786 C5101890!5101890 !27748847     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27748847 &cmd=llinks): Failed to open stream: HTTP request failed! 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Glycogen synthase kinase?3? is required for epithelial?mesenchymal transition and barrier dysfunction in mouse podocytes under high glucose conditions |pdf=|usr=}}{{27748847 }} gab.com Text Glycogen synthase kinase 3 is required for epithelial mesenchymal transition and barrier dysfunction in mouse podocytes under high glucose conditions JO: Mol Med Rep http://www.kidney.de/pget.php?&tw=1&pmid=27748847 #FOAvip Epithelial-mesenchymal transition (EMT) is important for diabetic nephropathy (DN). Podocytes are specialized epithelial cells, which form a major component of the glomerular filtration barrier. Podocyte damage has been suggested to be the primary mechanism behind the albuminuria associated with DN. The present study aimed to determine the function of glycogen synthase kinase (GSK)?3? in EMT and barrier dysfunction of mouse podocytes exposed to high glucose (HG) conditions. Matured and differentiated podocytes were treated with normal glucose (NG), HG or NG + mannitol. Podocytes were also transfected with a small interfering RNA (siRNA) against GSK?3? or a scrambled siRNA, or were treated with lithium chloride (LiCl), a GSK?3? inhibitor, under NG or HG conditions. The expression levels of the epithelial cell markers, nephrin and podocin, and the myofibroblast cell markers, ??smooth muscle actin (SMA) and fibronectin, in podocytes by western blot analysis and immunofluorescence staining, respectively. The monolayer barrier function was assessed by albumin inflow. The phosphorylation and activity levels of GSK?3? were also quantified. It was observed that HG promotes EMT in podocytes, due to the increased levels of podocin and nephrin expression and the reduced ??SMA and fibronectin expression levels. HG also induced barrier dysfunction and increased the expression level of total GSK?3?, Try216?phosphorylated?GSK?3? and the GSK?3? activity in podocytes. Transfection of GSK?3? siRNA or treatment with LiCl reversed the HG?induced EMT and barrier dysfunction in podocytes. In conclusion, the present study determined that GSK?3? is required for EMT and barrier dysfunction in podocytes under HG conditions; therefore, GSK?3? may be a novel target for the treatment of DN. Twit Text FOAVip Glycogen synthase kinase 3 is required for epithelial mesenchymal transition and barrier dysfunction in mouse podocytes under high glucose conditions ????Mol Med Rep http://www.kidney.de/pget.php?&tw=1&pmid=27748847 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27748847 #FOAvip English Wikipedia <ref>{{Cite pmid|27748847 }}</ref> Glycogen synthase kinase?3? is required for epithelial?mesenchymal transition and barrier dysfunction in mouse podocytes under high glucose conditions #MMPMID27748847 Guo J ; Yang L ; Qiao Y ; Liu Z Mol Med Rep 2016[Nov]; 14 (5 ): 4091-4098 PMID27748847 show ga Epithelial-mesenchymal transition (EMT) is important for diabetic nephropathy (DN). Podocytes are specialized epithelial cells, which form a major component of the glomerular filtration barrier. Podocyte damage has been suggested to be the primary mechanism behind the albuminuria associated with DN. The present study aimed to determine the function of glycogen synthase kinase (GSK)?3? in EMT and barrier dysfunction of mouse podocytes exposed to high glucose (HG) conditions. Matured and differentiated podocytes were treated with normal glucose (NG), HG or NG + mannitol. Podocytes were also transfected with a small interfering RNA (siRNA) against GSK?3? or a scrambled siRNA, or were treated with lithium chloride (LiCl), a GSK?3? inhibitor, under NG or HG conditions. The expression levels of the epithelial cell markers, nephrin and podocin, and the myofibroblast cell markers, ??smooth muscle actin (SMA) and fibronectin, in podocytes by western blot analysis and immunofluorescence staining, respectively. The monolayer barrier function was assessed by albumin inflow. The phosphorylation and activity levels of GSK?3? were also quantified. It was observed that HG promotes EMT in podocytes, due to the increased levels of podocin and nephrin expression and the reduced ??SMA and fibronectin expression levels. HG also induced barrier dysfunction and increased the expression level of total GSK?3?, Try216?phosphorylated?GSK?3? and the GSK?3? activity in podocytes. Transfection of GSK?3? siRNA or treatment with LiCl reversed the HG?induced EMT and barrier dysfunction in podocytes. In conclusion, the present study determined that GSK?3? is required for EMT and barrier dysfunction in podocytes under HG conditions; therefore, GSK?3? may be a novel target for the treatment of DN. |Actins/biosynthesis [MESH] |Animals [MESH] |Diabetic Nephropathies/*genetics/metabolism/pathology [MESH] |Disease Models, Animal [MESH] |Epithelial-Mesenchymal Transition/genetics [MESH] |Gene Expression Regulation/drug effects [MESH] |Glomerular Filtration Barrier/*metabolism/pathology [MESH] |Glucose/toxicity [MESH] |Glycogen Synthase Kinase 3 beta/antagonists & inhibitors/*genetics/metabolism [MESH] |Humans [MESH] |Intracellular Signaling Peptides and Proteins/biosynthesis [MESH] |Lithium Chloride/administration & dosage [MESH] |Membrane Proteins/biosynthesis [MESH] |Mice [MESH] |Podocytes/*metabolism/pathology [MESH]Glycogen synthase kinase?3? is required for epithelial?mesenchymal tra(epmc).pdf DeepDyve Pubget Overpricing