Monoclonal Antibody to CD31 (PECAM-1) Inhibits Tubular Regeneration after Ischemia Reperfusion Injury in the Rat

被引:1
作者
Valentini, Xavier
Gossiaux, Annabel
Caron, Nathalie [3 ]
Nonclercq, Denis
Legrand, Alexandre [2 ]
Toubeau, Gerard [1 ]
机构
[1] Univ Mons, Fac Med & Pharm, Serv Histol, Histol Lab, BE-7000 Mons, Belgium
[2] Univ Mons, Fac Med & Pharm, Lab Physiol & Pharmacol, BE-7000 Mons, Belgium
[3] Fac Univ Notre Dame Paix, Fac Med, Lab Gen Physiol, B-5000 Namur, Belgium
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2011年 / 118卷 / 03期
关键词
Acute renal failure; Cystic tubules; Kidney regeneration; Stem cells; Tubular necrosis; STEM-CELLS; KIDNEY; IDENTIFICATION; NEUTROPHILS; CISPLATIN; MIGRATION; MOLECULE; REPAIR; EGF;
D O I
10.1159/000322481
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aims: We used a rat model of renal ischemia (35 min) to test the potential involvement of platelet/endothelial cell adhesion molecule 1 (PECAM-1/CD31) in the process of S3 tubule regeneration. Methods: A monoclonal antibody specific for murine PECAM-1 was injected i.p. immediately after kidney reperfusion or 48 h post-ischemia. One day before ischemia, each animal received an i.p. injection of 80 mg/kg 5-bromo-2'-deoxyuridine (BrdU). Experimental animals were sacrificed 1, 2, 3, 7 and 14 days post-ischemia. Renal sections were processed to characterize the histopathological alterations and the distribution of BrdU-immunopositive cells. Results: Our observations showed that anti-PECAM-1 administration was associated with an inhibition of S3 tubule regeneration along with a progressive cystic dilatation of renal tubules that was particularly prominent 2 weeks post-ischemia. Interestingly, injection of anti-PECAM-1 48 h post-ischemia failed to block renal regeneration and was followed by a normal re-epithelialization of S3 tubules. Conclusion: Our data showed that the blockade of PECAM-1 immediately after kidney reperfusion inhibits tubular regeneration. These observations suggest that transendothelial migration of extrarenal cells could be a precocious and pivotal step in kidney reparation, but also suggest that these extrarenal cells could be essential to the process of tubular regeneration. Copyright (C) 2011 S. Karger AG, Basel
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页码:E60 / E68
页数:9
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