Mesenchymal stem cells home to injured tissues when co-infused with hematopoietic cells to treat a radiation-induced multi-organ failure syndrome

被引:362
作者
Chapel, A
Bertho, JM
Bensidhoum, M
Fouillard, L
Young, RG
Frick, J
Demarquay, C
Cuvelier, F
Mathieu, E
Trompier, F
Dudoignon, N
Germain, C
Mazurier, C
Aigueperse, J
Borneman, J
Gorin, NC
Gourmelon, P
Thierry, D
机构
[1] Inst Radioprotect & Surete Nucl, DPHD, SARAM, F-92262 Fontenay Aux Roses, France
[2] CHU St Antoine, Lab Therapie Cellulaire & Radioprotect Accidentel, UPRES 1632, Paris, France
[3] Osiris Therapeut Inc, Baltimore, MD USA
[4] Hop St Antoine, Serv Malad Sang, F-75571 Paris, France
关键词
ex vivo expansion; hematopoietic cell; mesenchymal stem cell; irradiation; homing; aplasia;
D O I
10.1002/jgm.452
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Background Recent studies have suggested that ex vivo expansion of autologous hematopoietic cells could be a therapy of choice for the treatment of bone marrow failure. We investigated the potential of a combined infusion of autologous ex vivo expanded hematopoietic cells with mesenchymal (MSCs) for the treatment of multiorgan failure syndrome following irradiation in a non-human primate model. Methods Hematopoietic cells and MSCs were expanded from bone marrow aspirates. MSCs were transduced with the gene encoding for the green fluorescent protein (e-GFP), in order to track them following infusion. Twelve animals were studied. Nine animals received total-body irradiation at 8 Gy from a neutron/gamma source thus resulting in heterogeneous exposure; three animals were sham-irradiated. The animals were treated with expanded hematopoietic stem cells and MSCs, expanded hematopoietic stem cells alone, or MSCs alone. Unmanipulated bone marrow cell transplants were used as controls. Results Depending on the neutron/gamma ratio, an acute radiation sickness of varying severity but of similar nature resulted. GFP-labeled cells were found in the injured muscle, skin, bone marrow and gut of the treated animals via PCR up to 82 days post-infusion. Conclusions This is the first evidence of expanded MSCs homing in numerous tissues following a severe multi-organ injury in primates. Localization of the transduced MSCs correlated to the severity and geometry of irradiation. A repair process was observed in various tissues. The plasticity potential of the MSCs and their contribution to the repair process in vivo remains to be studied. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:1028 / 1038
页数:11
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