Volume 69, Issue 12, Pages (June 2006)

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Volume 69, Issue 12, Pages 2186-2193 (June 2006) ABC transporter expression profiling after ischemic reperfusion injury in mouse kidney  M. Huls, J.J.M.W. van den Heuvel, H.B.P.M. Dijkman, F.G.M. Russel, R. Masereeuw  Kidney International  Volume 69, Issue 12, Pages 2186-2193 (June 2006) DOI: 10.1038/sj.ki.5000407 Copyright © 2006 International Society of Nephrology Terms and Conditions

Figure 1 Histopathology of the mouse kidney. Characteristic histologic signs of renal injury and regeneration after an ischemic insult. (a) Control kidney slice showing a glomerulus (G) surrounded by proximal tubules (P). (b) Two days after bilateral clamping of the renal artery and vein for 30 min, serious damage to the proximal tubules (P) is observed with debris in tubular lumen (indicated by arrows). (c) Seven days after the insult, the tubules are partially recovered as can be concluded from repaired brush border membranes (indicated by arrows). (d) Almost completely restored tubular segments (indicated by arrows) were found after 14 days. Original magnification, (all the figures) × 400 . Kidney International 2006 69, 2186-2193DOI: (10.1038/sj.ki.5000407) Copyright © 2006 International Society of Nephrology Terms and Conditions

Figure 2 Effect of kidney ischemia–reperfusion on renal creatinine handling. Creatinine clearances from sham-operated mice and mice that underwent bilateral ischemia for 30 min followed by 7 days of recovery. Data are presented as mean±s.e.m. of eight independent experiments. *Significantly different from basal value (P<0.001). Kidney International 2006 69, 2186-2193DOI: (10.1038/sj.ki.5000407) Copyright © 2006 International Society of Nephrology Terms and Conditions

Figure 3 Immunoblot analyses of ABC proteins in FVB mice before and 7 days after inducing ischemia. Total membrane fractions of mice kidneys were isolated and analyzed for expression of (a) abca3, (b) abcb1, (c) abcb11, (d) abcc2, (e) abcc4, and (f) abcg2. Values are means±s.e., n=4, where pixel intensity (arbitrary units) was set at 1.0 in the control. Significantly different from control (*P<0.05, **P<0.01, ***P<0.001). Kidney International 2006 69, 2186-2193DOI: (10.1038/sj.ki.5000407) Copyright © 2006 International Society of Nephrology Terms and Conditions

Figure 4 Renal distribution of mouse abca3, abcb11, and abcg2. (a) Representative immunohistochemical images show that abca3 is expressed in the peritubulary capillaries (indicated by arrows) and the apical membranes of the proximal tubules (*). (b) In addition, abca3 is expressed in Bowman's capsule (B). (c and d) Abcb11 is expressed in the apical membrane of the proximal tubules, as observed using two different antibodies (c: antibody from Kamiya Biomedical Company, Seattle, WA, USA; (d) antibody from professor Dr B Stieger, University Hospital Zürich, Switzerland). (e) Abcc4 expression seen in the apical membrane of the proximal tubules. (f) After double staining with Na+, K+-ATPase, which is localized to the basolateral membrane, it is clear that abcg2 is expressed in the apical membrane of the proximal tubules. G, glomerulus; B, Bowman's capsule, P, proximal tubule, D, distal tubule (original magnification, (a and b) × 500; (c) × 200; (d–f) × 400). Kidney International 2006 69, 2186-2193DOI: (10.1038/sj.ki.5000407) Copyright © 2006 International Society of Nephrology Terms and Conditions