Intra-arterial transplantation of stem cells in large animals as a minimally-invasive strategy for the treatment of disseminated neurodegeneration
Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells....
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Published in | Scientific reports Vol. 11; no. 1; pp. 6581 - 10 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Nature Publishing Group UK
22.03.2021
Nature Publishing Group Nature Portfolio |
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Abstract | Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells. The goal of this study was to investigate the feasibility and safety of MRI-guided transplantation of glial restricted precursors (GRPs) and mesenchymal stem cells (MSCs) in dogs suffering from ALS-like disease, degenerative myelopathy (DM). Canine GRP transplantation in dogs resulted in rather poor retention in the brain, so MSCs were used in subsequent experiments. To evaluate the safety of MSC intraarterial transplantation, naïve pigs (n = 3) were used as a pre-treatment control before transplantation in dogs. Cells were labeled with iron oxide nanoparticles. For IA transplantation a 1.2-French microcatheter was advanced into the middle cerebral artery under roadmap guidance. Then, the cells were transplanted under real-time MRI with the acquisition of dynamic T2*-weighted images. The procedure in pigs has proven to be safe and histopathology has demonstrated the successful and predictable placement of transplanted porcine MSCs. Transplantation of canine MSCs in DM dogs resulted in their accumulation in the brain. Interventional and follow-up MRI proved the procedure was feasible and safe. Analysis of gene expression after transplantation revealed a reduction of inflammatory factors, which may indicate a promising therapeutic strategy in the treatment of neurodegenerative diseases. |
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AbstractList | Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells. The goal of this study was to investigate the feasibility and safety of MRI-guided transplantation of glial restricted precursors (GRPs) and mesenchymal stem cells (MSCs) in dogs suffering from ALS-like disease, degenerative myelopathy (DM). Canine GRP transplantation in dogs resulted in rather poor retention in the brain, so MSCs were used in subsequent experiments. To evaluate the safety of MSC intraarterial transplantation, naïve pigs (n = 3) were used as a pre-treatment control before transplantation in dogs. Cells were labeled with iron oxide nanoparticles. For IA transplantation a 1.2-French microcatheter was advanced into the middle cerebral artery under roadmap guidance. Then, the cells were transplanted under real-time MRI with the acquisition of dynamic T2*-weighted images. The procedure in pigs has proven to be safe and histopathology has demonstrated the successful and predictable placement of transplanted porcine MSCs. Transplantation of canine MSCs in DM dogs resulted in their accumulation in the brain. Interventional and follow-up MRI proved the procedure was feasible and safe. Analysis of gene expression after transplantation revealed a reduction of inflammatory factors, which may indicate a promising therapeutic strategy in the treatment of neurodegenerative diseases.Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells. The goal of this study was to investigate the feasibility and safety of MRI-guided transplantation of glial restricted precursors (GRPs) and mesenchymal stem cells (MSCs) in dogs suffering from ALS-like disease, degenerative myelopathy (DM). Canine GRP transplantation in dogs resulted in rather poor retention in the brain, so MSCs were used in subsequent experiments. To evaluate the safety of MSC intraarterial transplantation, naïve pigs (n = 3) were used as a pre-treatment control before transplantation in dogs. Cells were labeled with iron oxide nanoparticles. For IA transplantation a 1.2-French microcatheter was advanced into the middle cerebral artery under roadmap guidance. Then, the cells were transplanted under real-time MRI with the acquisition of dynamic T2*-weighted images. The procedure in pigs has proven to be safe and histopathology has demonstrated the successful and predictable placement of transplanted porcine MSCs. Transplantation of canine MSCs in DM dogs resulted in their accumulation in the brain. Interventional and follow-up MRI proved the procedure was feasible and safe. Analysis of gene expression after transplantation revealed a reduction of inflammatory factors, which may indicate a promising therapeutic strategy in the treatment of neurodegenerative diseases. Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells. The goal of this study was to investigate the feasibility and safety of MRI-guided transplantation of glial restricted precursors (GRPs) and mesenchymal stem cells (MSCs) in dogs suffering from ALS-like disease, degenerative myelopathy (DM). Canine GRP transplantation in dogs resulted in rather poor retention in the brain, so MSCs were used in subsequent experiments. To evaluate the safety of MSC intraarterial transplantation, naïve pigs (n = 3) were used as a pre-treatment control before transplantation in dogs. Cells were labeled with iron oxide nanoparticles. For IA transplantation a 1.2-French microcatheter was advanced into the middle cerebral artery under roadmap guidance. Then, the cells were transplanted under real-time MRI with the acquisition of dynamic T2*-weighted images. The procedure in pigs has proven to be safe and histopathology has demonstrated the successful and predictable placement of transplanted porcine MSCs. Transplantation of canine MSCs in DM dogs resulted in their accumulation in the brain. Interventional and follow-up MRI proved the procedure was feasible and safe. Analysis of gene expression after transplantation revealed a reduction of inflammatory factors, which may indicate a promising therapeutic strategy in the treatment of neurodegenerative diseases. Abstract Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery of cells and their broad distribution is challenging. To address this problem, we explored intra-arterial (IA) delivery route, of stem cells. The goal of this study was to investigate the feasibility and safety of MRI-guided transplantation of glial restricted precursors (GRPs) and mesenchymal stem cells (MSCs) in dogs suffering from ALS-like disease, degenerative myelopathy (DM). Canine GRP transplantation in dogs resulted in rather poor retention in the brain, so MSCs were used in subsequent experiments. To evaluate the safety of MSC intraarterial transplantation, naïve pigs (n = 3) were used as a pre-treatment control before transplantation in dogs. Cells were labeled with iron oxide nanoparticles. For IA transplantation a 1.2-French microcatheter was advanced into the middle cerebral artery under roadmap guidance. Then, the cells were transplanted under real-time MRI with the acquisition of dynamic T2*-weighted images. The procedure in pigs has proven to be safe and histopathology has demonstrated the successful and predictable placement of transplanted porcine MSCs. Transplantation of canine MSCs in DM dogs resulted in their accumulation in the brain. Interventional and follow-up MRI proved the procedure was feasible and safe. Analysis of gene expression after transplantation revealed a reduction of inflammatory factors, which may indicate a promising therapeutic strategy in the treatment of neurodegenerative diseases. |
ArticleNumber | 6581 |
Author | Zawadzki, Michal Milewska, Kamila Kalkowski, Lukasz Głodek, Joanna Sanford, Joanna Golubczyk, Dominika Walczak, Piotr Malysz-Cymborska, Izabela Janowski, Miroslaw Kwiatkowska, Joanna Holak, Piotr Adamiak, Zbigniew |
Author_xml | – sequence: 1 givenname: Izabela orcidid: 0000-0003-4192-6726 surname: Malysz-Cymborska fullname: Malysz-Cymborska, Izabela email: i.m.cymborska@gmail.com organization: Department of Neurosurgery, School of Medicine, Collegium Medicum, University of Warmia and Mazury – sequence: 2 givenname: Dominika surname: Golubczyk fullname: Golubczyk, Dominika organization: Department of Neurosurgery, School of Medicine, Collegium Medicum, University of Warmia and Mazury – sequence: 3 givenname: Lukasz surname: Kalkowski fullname: Kalkowski, Lukasz organization: Department of Neurosurgery, School of Medicine, Collegium Medicum, University of Warmia and Mazury – sequence: 4 givenname: Joanna surname: Kwiatkowska fullname: Kwiatkowska, Joanna organization: Department of Neurosurgery, School of Medicine, Collegium Medicum, University of Warmia and Mazury – sequence: 5 givenname: Michal surname: Zawadzki fullname: Zawadzki, Michal organization: Central Clinical Hospital of Ministry of the Interior and Administration in Warsaw – sequence: 6 givenname: Joanna surname: Głodek fullname: Głodek, Joanna organization: Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Warmia and Mazury – sequence: 7 givenname: Piotr surname: Holak fullname: Holak, Piotr organization: Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Warmia and Mazury – sequence: 8 givenname: Joanna surname: Sanford fullname: Sanford, Joanna organization: Sanford Biotech – sequence: 9 givenname: Kamila surname: Milewska fullname: Milewska, Kamila organization: Department of Neurosurgery, School of Medicine, Collegium Medicum, University of Warmia and Mazury – sequence: 10 givenname: Zbigniew surname: Adamiak fullname: Adamiak, Zbigniew organization: Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Warmia and Mazury – sequence: 11 givenname: Piotr surname: Walczak fullname: Walczak, Piotr organization: Center for Advanced Imaging Research and Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine – sequence: 12 givenname: Miroslaw surname: Janowski fullname: Janowski, Miroslaw organization: Center for Advanced Imaging Research and Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine |
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Snippet | Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS, delivery... Abstract Stem cell transplantation proved promising in animal models of neurological diseases; however, in conditions with disseminated pathology such as ALS,... |
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SubjectTerms | 631/378 631/378/1687 631/378/1689 631/378/2183 Amyotrophic lateral sclerosis Animal diseases Animal models Central nervous system diseases Dogs Gene expression Glial stem cells Histopathology Humanities and Social Sciences Inflammation Iron oxides Magnetic resonance imaging Mesenchyme multidisciplinary Nanoparticles Neurodegeneration Neurodegenerative diseases Neurological diseases Science Science (multidisciplinary) Spinal cord Stem cell transplantation Stem cells Transplantation |
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Title | Intra-arterial transplantation of stem cells in large animals as a minimally-invasive strategy for the treatment of disseminated neurodegeneration |
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