Volume 56, Issue 5, Pages (November 1999)

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Volume 56, Issue 5, Pages 1737-1750 (November 1999) Differential expression of protein kinase C isoforms in streptozotocin-induced diabetic rats  Ningling Kang, Gabriele Alexander, Joon Keun Park, Christian Maasch, Igor Buchwalow, Friedrich C. Luft, Hermann Haller, M.D.  Kidney International  Volume 56, Issue 5, Pages 1737-1750 (November 1999) DOI: 10.1046/j.1523-1755.1999.00725.x Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 1 Immunohistochemistry of PKC isoform α in kidneys (A–D) and heart (E and F) from normoglycemic (left panels) and hyperglycemic animals (right panels). In renal tissue from normoglycemic rats, PKC α was faintly expressed in the glomeruli and apical tubules (A). Hyperglycemia increased PKC α expression in the glomeruli and the interstitial space (B). Hyperglycemia also induced and increased expression in the endothelium and in the perivascular space (C and D). Similar changes were present in the vessels of the heart (E and F). Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 2 Immunohistochemistry of PKC β (common antibody; A–D) and PKC δ (E–H) in kidney (A and B, E and F), and myocardium (C and D, G and H) of normoglycemic (left panel) and hyperglycemic rats (right panel). Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 3 Immunohistochemistry of PKC βI (A–D) and PKC βII (E–H) in kidney (A and B, E and F), and myocardium (C and D, G and H) of normoglycemic (left panel) and hyperglycemic rats (right panel). Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 4 Immunohistochemistry of PKC ϵ (A–D) and PKC ζ (E–H) in kidney (A and B, E and F), and myocardium (C and D, G and H) of normoglycemic (left panel) and hyperglycemic rats (right panel). Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 5 Protein expression (A) and translocation (B and C) of PKC isoforms α, βI, βII, δ, ϵ, and ζ in renal tissue of normoglycemic control (c) and hyperglycemic (gl) rats. For the translocation experiments, renal cortical tissue was fractionated by ultracentrifugation, and the cytosolic and particulate fractions were analyzed. Bars represent the densitometric analysis of more than experiments. Symbols in C are: () particulate fraction; () cytosolic fraction; (□) control; (▪) hyperglycemia. Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 6 Western blotting of PKC isoforms α, βI, βII, δ, ϵ, and ζ in myocardial tissue of normal and hyperglycemic rats. Bars are densitometric analysis of more than experiments. Symbols are: (□) control; (▪) hyperglycemia. Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions

Figure 7 Immunofluorescence of PKC α in renal tissue (A–D), skeletal muscle (E and F), and aorta (G and H) of normoglycemic (left panel) and hyperglycemic rats (right panel). Kidney International 1999 56, 1737-1750DOI: (10.1046/j.1523-1755.1999.00725.x) Copyright © 1999 International Society of Nephrology Terms and Conditions