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Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog
Osteoarthritis (OA) is a highly prevalent condition in dogs, causing a substantial reduction in quality of life and welfare of the animals. Current disease management focusses on pain relief but does not stop the progression of the disease. Therefore, mesenchymal stem cells (MSCs) could offer a prom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729935/ https://www.ncbi.nlm.nih.gov/pubmed/36504848 http://dx.doi.org/10.3389/fvets.2022.1035175 |
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author | Beerts, Charlotte Pauwelyn, Glenn Depuydt, Eva Xu, Yangfeng Saunders, Jimmy H. Peremans, Kathelijne Spaas, Jan H. |
author_facet | Beerts, Charlotte Pauwelyn, Glenn Depuydt, Eva Xu, Yangfeng Saunders, Jimmy H. Peremans, Kathelijne Spaas, Jan H. |
author_sort | Beerts, Charlotte |
collection | PubMed |
description | Osteoarthritis (OA) is a highly prevalent condition in dogs, causing a substantial reduction in quality of life and welfare of the animals. Current disease management focusses on pain relief but does not stop the progression of the disease. Therefore, mesenchymal stem cells (MSCs) could offer a promising disease modifying alternative. However, little is known about the behavior and the mode of action of MSCs following their administration. In the current case report, (99m)Technetium labelled xenogeneic equine peripheral blood-derived MSCs were intravenously injected in a 9 year old dog suffering from a natural occurring cranial cruciate ligament rupture. The biodistribution of the MSCs was evaluated during a 6-h follow-up period, using a full body scintigraphy imaging technique. No clinical abnormalities or ectopic tissue formations were detected throughout the study. A radiopharmaceutical uptake was present in the liver, heart, lung, spleen, kidneys and bladder of the dog. Furthermore, homing of the radiolabelled MSCs to the injured joint was observed, with 40.61 % higher uptake in the affected joint in comparison with the healthy contralateral joint. Finally, a local radioactive hotspot was seen at a part of the tail of the dog that had been injured recently. The current study is the first to confirm the homing of xenogeneic MSCs to a naturally occurring joint lesion after IV administration. |
format | Online Article Text |
id | pubmed-9729935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97299352022-12-09 Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog Beerts, Charlotte Pauwelyn, Glenn Depuydt, Eva Xu, Yangfeng Saunders, Jimmy H. Peremans, Kathelijne Spaas, Jan H. Front Vet Sci Veterinary Science Osteoarthritis (OA) is a highly prevalent condition in dogs, causing a substantial reduction in quality of life and welfare of the animals. Current disease management focusses on pain relief but does not stop the progression of the disease. Therefore, mesenchymal stem cells (MSCs) could offer a promising disease modifying alternative. However, little is known about the behavior and the mode of action of MSCs following their administration. In the current case report, (99m)Technetium labelled xenogeneic equine peripheral blood-derived MSCs were intravenously injected in a 9 year old dog suffering from a natural occurring cranial cruciate ligament rupture. The biodistribution of the MSCs was evaluated during a 6-h follow-up period, using a full body scintigraphy imaging technique. No clinical abnormalities or ectopic tissue formations were detected throughout the study. A radiopharmaceutical uptake was present in the liver, heart, lung, spleen, kidneys and bladder of the dog. Furthermore, homing of the radiolabelled MSCs to the injured joint was observed, with 40.61 % higher uptake in the affected joint in comparison with the healthy contralateral joint. Finally, a local radioactive hotspot was seen at a part of the tail of the dog that had been injured recently. The current study is the first to confirm the homing of xenogeneic MSCs to a naturally occurring joint lesion after IV administration. Frontiers Media S.A. 2022-11-24 /pmc/articles/PMC9729935/ /pubmed/36504848 http://dx.doi.org/10.3389/fvets.2022.1035175 Text en Copyright © 2022 Beerts, Pauwelyn, Depuydt, Xu, Saunders, Peremans and Spaas. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Beerts, Charlotte Pauwelyn, Glenn Depuydt, Eva Xu, Yangfeng Saunders, Jimmy H. Peremans, Kathelijne Spaas, Jan H. Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title | Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title_full | Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title_fullStr | Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title_full_unstemmed | Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title_short | Homing of radiolabelled xenogeneic equine peripheral blood-derived MSCs towards a joint lesion in a dog |
title_sort | homing of radiolabelled xenogeneic equine peripheral blood-derived mscs towards a joint lesion in a dog |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729935/ https://www.ncbi.nlm.nih.gov/pubmed/36504848 http://dx.doi.org/10.3389/fvets.2022.1035175 |
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