Evaluation of the effect of autologous mesenchymal stem cell injection in a large-animal model of bilateral kidney ischaemia reperfusion injury

Objectives: Adult mesenchymal stem cells (MSC) have been proven to be of benefit to the kidney in different experimental models of renal injuries. All studies have been performed in valuable rodent models, but the relevance of these results to large mammals and ultimately, to humans remains unknown....

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Veröffentlicht in:Cell proliferation 2009-06, Vol.42 (3), p.284-297
Hauptverfasser: Behr, L., Hekmati, M., Lucchini, A., Houcinet, K., Faussat, A.-M., Borenstein, N., Noel, L.-H., Lelievre-Pegorier, M., Laborde, K.
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container_end_page 297
container_issue 3
container_start_page 284
container_title Cell proliferation
container_volume 42
creator Behr, L.
Hekmati, M.
Lucchini, A.
Houcinet, K.
Faussat, A.-M.
Borenstein, N.
Noel, L.-H.
Lelievre-Pegorier, M.
Laborde, K.
description Objectives: Adult mesenchymal stem cells (MSC) have been proven to be of benefit to the kidney in different experimental models of renal injuries. All studies have been performed in valuable rodent models, but the relevance of these results to large mammals and ultimately, to humans remains unknown. Therefore, the aim of this study was to investigate the effect of MSC transplantation in an alternative ovine large‐animal model of bilateral kidney ischaemia reperfusion injury. Material and methods: Sheep were divided into three groups: one sham‐operated group and two groups submitted to renal bilateral ischaemia for 60 min. Animals with ischaemia reperfusion injury were treated with injection of autologous MSCs or with vehicle medium. Results: The model sheep presented with renal histological manefestations that closely resembled lesions seen in patients. Transplanted MSCs were found in glomeruli but not in tubules and did not express glomerular cell markers (podocin, von Willebrand factor), but functional evaluation showed no beneficial effect of MSC infusion. Morphological and molecular analyses corroborated the functional results. MSCs did not repair kidney parenchyma and failed to modulate cell death and proliferation or cytokine release (tumour necrosis factor‐alpha, vascular endothelial growth factor alpha (VEGF‐α), Bcl‐2, caspase). Conclusion: In this unique autologous large‐animal model, MSCs did not exhibit reparative or paracrine protective properties.
doi_str_mv 10.1111/j.1365-2184.2009.00591.x
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All studies have been performed in valuable rodent models, but the relevance of these results to large mammals and ultimately, to humans remains unknown. Therefore, the aim of this study was to investigate the effect of MSC transplantation in an alternative ovine large‐animal model of bilateral kidney ischaemia reperfusion injury. Material and methods: Sheep were divided into three groups: one sham‐operated group and two groups submitted to renal bilateral ischaemia for 60 min. Animals with ischaemia reperfusion injury were treated with injection of autologous MSCs or with vehicle medium. Results: The model sheep presented with renal histological manefestations that closely resembled lesions seen in patients. Transplanted MSCs were found in glomeruli but not in tubules and did not express glomerular cell markers (podocin, von Willebrand factor), but functional evaluation showed no beneficial effect of MSC infusion. Morphological and molecular analyses corroborated the functional results. MSCs did not repair kidney parenchyma and failed to modulate cell death and proliferation or cytokine release (tumour necrosis factor‐alpha, vascular endothelial growth factor alpha (VEGF‐α), Bcl‐2, caspase). Conclusion: In this unique autologous large‐animal model, MSCs did not exhibit reparative or paracrine protective properties.</description><identifier>ISSN: 0960-7722</identifier><identifier>EISSN: 1365-2184</identifier><identifier>DOI: 10.1111/j.1365-2184.2009.00591.x</identifier><identifier>PMID: 19438896</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Base Sequence ; Cell Differentiation ; Cell Proliferation ; Disease Models, Animal ; DNA Primers ; Kidney - blood supply ; Mesenchymal Stromal Cells - cytology ; Original ; Polymerase Chain Reaction ; Reperfusion Injury - surgery ; Sheep ; Stem Cell Transplantation</subject><ispartof>Cell proliferation, 2009-06, Vol.42 (3), p.284-297</ispartof><rights>Journal compilation © 2009 Blackwell Publishing Ltd. 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Morphological and molecular analyses corroborated the functional results. MSCs did not repair kidney parenchyma and failed to modulate cell death and proliferation or cytokine release (tumour necrosis factor‐alpha, vascular endothelial growth factor alpha (VEGF‐α), Bcl‐2, caspase). 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subjects Animals
Base Sequence
Cell Differentiation
Cell Proliferation
Disease Models, Animal
DNA Primers
Kidney - blood supply
Mesenchymal Stromal Cells - cytology
Original
Polymerase Chain Reaction
Reperfusion Injury - surgery
Sheep
Stem Cell Transplantation
title Evaluation of the effect of autologous mesenchymal stem cell injection in a large-animal model of bilateral kidney ischaemia reperfusion injury
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