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
引用
收藏
页码:E60 / E68
页数:9
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