Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing
Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during w...
Ausführliche Beschreibung
Autor*in: |
Karlien Kallmeyer [verfasserIn] Dominik André‐Lévigne [verfasserIn] Mathurin Baquié [verfasserIn] Karl‐Heinz Krause [verfasserIn] Michael S. Pepper [verfasserIn] Brigitte Pittet‐Cuénod [verfasserIn] Ali Modarressi [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Übergeordnetes Werk: |
In: Stem Cells Translational Medicine - Oxford University Press, 2017, 9(2020), 1, Seite 131-144 |
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Übergeordnetes Werk: |
volume:9 ; year:2020 ; number:1 ; pages:131-144 |
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Link aufrufen |
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DOI / URN: |
10.1002/sctm.19-0091 |
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Katalog-ID: |
DOAJ017939933 |
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10.1002/sctm.19-0091 doi (DE-627)DOAJ017939933 (DE-599)DOAJa98f75522a6d4a80814f5f26eb0c62ac DE-627 ger DE-627 rakwb eng R5-920 QH573-671 Karlien Kallmeyer verfasserin aut Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. adipose‐derived mesenchymal stromal cells bioluminescence imaging firefly luciferase green fluorescent protein in vivo imaging wound healing Medicine (General) Cytology Dominik André‐Lévigne verfasserin aut Mathurin Baquié verfasserin aut Karl‐Heinz Krause verfasserin aut Michael S. Pepper verfasserin aut Brigitte Pittet‐Cuénod verfasserin aut Ali Modarressi verfasserin aut In Stem Cells Translational Medicine Oxford University Press, 2017 9(2020), 1, Seite 131-144 (DE-627)680320539 (DE-600)2642270-0 21576580 nnns volume:9 year:2020 number:1 pages:131-144 https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/article/a98f75522a6d4a80814f5f26eb0c62ac kostenfrei https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/toc/2157-6564 Journal toc kostenfrei https://doaj.org/toc/2157-6580 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020 1 131-144 |
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10.1002/sctm.19-0091 doi (DE-627)DOAJ017939933 (DE-599)DOAJa98f75522a6d4a80814f5f26eb0c62ac DE-627 ger DE-627 rakwb eng R5-920 QH573-671 Karlien Kallmeyer verfasserin aut Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. adipose‐derived mesenchymal stromal cells bioluminescence imaging firefly luciferase green fluorescent protein in vivo imaging wound healing Medicine (General) Cytology Dominik André‐Lévigne verfasserin aut Mathurin Baquié verfasserin aut Karl‐Heinz Krause verfasserin aut Michael S. Pepper verfasserin aut Brigitte Pittet‐Cuénod verfasserin aut Ali Modarressi verfasserin aut In Stem Cells Translational Medicine Oxford University Press, 2017 9(2020), 1, Seite 131-144 (DE-627)680320539 (DE-600)2642270-0 21576580 nnns volume:9 year:2020 number:1 pages:131-144 https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/article/a98f75522a6d4a80814f5f26eb0c62ac kostenfrei https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/toc/2157-6564 Journal toc kostenfrei https://doaj.org/toc/2157-6580 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020 1 131-144 |
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10.1002/sctm.19-0091 doi (DE-627)DOAJ017939933 (DE-599)DOAJa98f75522a6d4a80814f5f26eb0c62ac DE-627 ger DE-627 rakwb eng R5-920 QH573-671 Karlien Kallmeyer verfasserin aut Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. adipose‐derived mesenchymal stromal cells bioluminescence imaging firefly luciferase green fluorescent protein in vivo imaging wound healing Medicine (General) Cytology Dominik André‐Lévigne verfasserin aut Mathurin Baquié verfasserin aut Karl‐Heinz Krause verfasserin aut Michael S. Pepper verfasserin aut Brigitte Pittet‐Cuénod verfasserin aut Ali Modarressi verfasserin aut In Stem Cells Translational Medicine Oxford University Press, 2017 9(2020), 1, Seite 131-144 (DE-627)680320539 (DE-600)2642270-0 21576580 nnns volume:9 year:2020 number:1 pages:131-144 https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/article/a98f75522a6d4a80814f5f26eb0c62ac kostenfrei https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/toc/2157-6564 Journal toc kostenfrei https://doaj.org/toc/2157-6580 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020 1 131-144 |
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10.1002/sctm.19-0091 doi (DE-627)DOAJ017939933 (DE-599)DOAJa98f75522a6d4a80814f5f26eb0c62ac DE-627 ger DE-627 rakwb eng R5-920 QH573-671 Karlien Kallmeyer verfasserin aut Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. adipose‐derived mesenchymal stromal cells bioluminescence imaging firefly luciferase green fluorescent protein in vivo imaging wound healing Medicine (General) Cytology Dominik André‐Lévigne verfasserin aut Mathurin Baquié verfasserin aut Karl‐Heinz Krause verfasserin aut Michael S. Pepper verfasserin aut Brigitte Pittet‐Cuénod verfasserin aut Ali Modarressi verfasserin aut In Stem Cells Translational Medicine Oxford University Press, 2017 9(2020), 1, Seite 131-144 (DE-627)680320539 (DE-600)2642270-0 21576580 nnns volume:9 year:2020 number:1 pages:131-144 https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/article/a98f75522a6d4a80814f5f26eb0c62ac kostenfrei https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/toc/2157-6564 Journal toc kostenfrei https://doaj.org/toc/2157-6580 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020 1 131-144 |
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10.1002/sctm.19-0091 doi (DE-627)DOAJ017939933 (DE-599)DOAJa98f75522a6d4a80814f5f26eb0c62ac DE-627 ger DE-627 rakwb eng R5-920 QH573-671 Karlien Kallmeyer verfasserin aut Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. adipose‐derived mesenchymal stromal cells bioluminescence imaging firefly luciferase green fluorescent protein in vivo imaging wound healing Medicine (General) Cytology Dominik André‐Lévigne verfasserin aut Mathurin Baquié verfasserin aut Karl‐Heinz Krause verfasserin aut Michael S. Pepper verfasserin aut Brigitte Pittet‐Cuénod verfasserin aut Ali Modarressi verfasserin aut In Stem Cells Translational Medicine Oxford University Press, 2017 9(2020), 1, Seite 131-144 (DE-627)680320539 (DE-600)2642270-0 21576580 nnns volume:9 year:2020 number:1 pages:131-144 https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/article/a98f75522a6d4a80814f5f26eb0c62ac kostenfrei https://doi.org/10.1002/sctm.19-0091 kostenfrei https://doaj.org/toc/2157-6564 Journal toc kostenfrei https://doaj.org/toc/2157-6580 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020 1 131-144 |
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Fate of systemically and locally administered adipose‐derived mesenchymal stromal cells and their effect on wound healing |
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Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. |
abstractGer |
Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. |
abstract_unstemmed |
Abstract There is increasing interest in the use of adipose‐derived mesenchymal stromal cells (ASCs) for wound repair. As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed. |
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As the fate of administered cells is still poorly defined, we aimed to establish the location, survival, and effect of ASCs when administered either systemically or locally during wound repair under physiological conditions. To determine the behavior of ASCs, a rat model with wounds on the dorsal aspect of the hind paws was used and two treatment modes were assessed: ASCs administered systemically into the tail vein or locally around the wound. ASCs were transduced to express both firefly luciferase (Fluc) and green fluorescent protein to enable tracking by bioluminescence imaging and immunohistological analysis. Systemically administered ASCs were detected in the lungs 3 hours after injection with a decrease in luminescent signal at 48 hours and signal disappearance from 72 hours. No ASCs were detected in the wound. Locally administered ASCs remained strongly detectable for 7 days at the injection site and became distributed within the wound bed as early as 24 hours post injection with a significant increase observed at 72 hours. Systemically administered ASCs were filtered out in the lungs, whereas ASCs administered locally remained and survived not only at the injection site but were also detected within the wound bed. Both treatments led to enhanced wound closure. It appears that systemically administered ASCs have the potential to enhance wound repair distally from their site of entrapment in the lungs whereas locally administered ASCs enhanced wound repair as they became redistributed within the wound bed.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">adipose‐derived mesenchymal stromal cells</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">bioluminescence imaging</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">firefly luciferase</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">green fluorescent protein</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">in vivo imaging</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">wound healing</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Medicine (General)</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Cytology</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Dominik André‐Lévigne</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Mathurin Baquié</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Karl‐Heinz Krause</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Michael S. 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