Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation
There is little information on the fate of infused mesenchymal stem cells (MSCs) and long-term side effects after irradiation exposure. We addressed these questions using human MSCs (hMSCs) intravenously infused to nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice submitted to total...
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doaj-51e22830caa84d81b24966bd6a94939a2020-11-24T22:16:18ZengHindawi LimitedStem Cells International1687-966X1687-96782014-01-01201410.1155/2014/939275939275Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following IrradiationSabine François0Benoit Usunier1Luc Douay2Marc Benderitter3Alain Chapel4PRP-HOM, SRBE, Laboratory of Radiopathology and Experimental Therapy, Radiological Protection and Human Health Division, Institute of Radiological Protection and Nuclear Safety, 92260 Fontenay-aux-Roses, FrancePRP-HOM, SRBE, Laboratory of Radiopathology and Experimental Therapy, Radiological Protection and Human Health Division, Institute of Radiological Protection and Nuclear Safety, 92260 Fontenay-aux-Roses, FranceUMRS 938 Department of Hematology, Saint Antoine Hospital APHP and UPMC University, 75012 Paris, FrancePRP-HOM, SRBE, Laboratory of Radiopathology and Experimental Therapy, Radiological Protection and Human Health Division, Institute of Radiological Protection and Nuclear Safety, 92260 Fontenay-aux-Roses, FrancePRP-HOM, SRBE, Laboratory of Radiopathology and Experimental Therapy, Radiological Protection and Human Health Division, Institute of Radiological Protection and Nuclear Safety, 92260 Fontenay-aux-Roses, FranceThere is little information on the fate of infused mesenchymal stem cells (MSCs) and long-term side effects after irradiation exposure. We addressed these questions using human MSCs (hMSCs) intravenously infused to nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice submitted to total body irradiation (TBI) or local irradiation (abdominal or leg irradiation). The animals were sacrificed 3 to 120 days after irradiation and the quantitative and spatial distribution of hMSCs were studied by polymerase chain reaction (PCR). Following their infusion into nonirradiated animals, hMSCs homed to various tissues. Engraftment depended on the dose of irradiation and the area exposed. Total body irradiation induced an increased hMSC engraftment level compared to nonirradiated mice, while local irradiations increased hMSC engraftment locally in the area of irradiation. Long-term engraftment of systemically administered hMSCs in NOD/SCID mice increased significantly in response to tissue injuries produced by local or total body irradiation until 2 weeks then slowly decreased depending on organs and the configuration of irradiation. In all cases, no tissue abnormality or abnormal hMSCs proliferation was observed at 120 days after irradiation. This work supports the safe and efficient use of MSCs by injection as an alternative approach in the short- and long-term treatment of severe complications after radiotherapy for patients refractory to conventional treatments.http://dx.doi.org/10.1155/2014/939275 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sabine François Benoit Usunier Luc Douay Marc Benderitter Alain Chapel |
spellingShingle |
Sabine François Benoit Usunier Luc Douay Marc Benderitter Alain Chapel Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation Stem Cells International |
author_facet |
Sabine François Benoit Usunier Luc Douay Marc Benderitter Alain Chapel |
author_sort |
Sabine François |
title |
Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation |
title_short |
Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation |
title_full |
Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation |
title_fullStr |
Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation |
title_full_unstemmed |
Long-Term Quantitative Biodistribution and Side Effects of Human Mesenchymal Stem Cells (hMSCs) Engraftment in NOD/SCID Mice following Irradiation |
title_sort |
long-term quantitative biodistribution and side effects of human mesenchymal stem cells (hmscs) engraftment in nod/scid mice following irradiation |
publisher |
Hindawi Limited |
series |
Stem Cells International |
issn |
1687-966X 1687-9678 |
publishDate |
2014-01-01 |
description |
There is little information on the fate of infused mesenchymal stem cells (MSCs) and long-term side effects after irradiation exposure. We addressed these questions using human MSCs (hMSCs) intravenously infused to nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice submitted to total body irradiation (TBI) or local irradiation (abdominal or leg irradiation). The animals were sacrificed 3 to 120 days after irradiation and the quantitative and spatial distribution of hMSCs were studied by polymerase chain reaction (PCR). Following their infusion into nonirradiated animals, hMSCs homed to various tissues. Engraftment depended on the dose of irradiation and the area exposed. Total body irradiation induced an increased hMSC engraftment level compared to nonirradiated mice, while local irradiations increased hMSC engraftment locally in the area of irradiation. Long-term engraftment of systemically administered hMSCs in NOD/SCID mice increased significantly in response to tissue injuries produced by local or total body irradiation until 2 weeks then slowly decreased depending on organs and the configuration of irradiation. In all cases, no tissue abnormality or abnormal hMSCs proliferation was observed at 120 days after irradiation. This work supports the safe and efficient use of MSCs by injection as an alternative approach in the short- and long-term treatment of severe complications after radiotherapy for patients refractory to conventional treatments. |
url |
http://dx.doi.org/10.1155/2014/939275 |
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