Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury
Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regenera...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Mukhamedshina, Y. O. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2017 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer Science+Business Media, LLC 2017 |
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| Übergeordnetes Werk: |
Enthalten in: BioNanoScience - New York, NY [u.a.] : Springer, 2011, 7(2017), 4 vom: 08. Aug., Seite 608-612 |
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| Übergeordnetes Werk: |
volume:7 ; year:2017 ; number:4 ; day:08 ; month:08 ; pages:608-612 |
| Links: |
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| DOI / URN: |
10.1007/s12668-017-0440-0 |
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| Katalog-ID: |
SPR026910977 |
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| 100 | 1 | |a Mukhamedshina, Y. O. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury |
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| 520 | |a Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. | ||
| 650 | 4 | |a Adipose-derived mesenchymal stem cells |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Spinal cord injury |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Migration |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Zakirova, E. Yu. |4 aut | |
| 700 | 1 | |a Galieva, L. R. |4 aut | |
| 700 | 1 | |a Kostennikov, A. A. |4 aut | |
| 700 | 1 | |a Akhmetzyanova, E. R. |4 aut | |
| 700 | 1 | |a Rizvanov, A. A. |4 aut | |
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10.1007/s12668-017-0440-0 doi (DE-627)SPR026910977 (SPR)s12668-017-0440-0-e DE-627 ger DE-627 rakwb eng Mukhamedshina, Y. O. verfasserin aut Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC 2017 Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 Zakirova, E. Yu. aut Galieva, L. R. aut Kostennikov, A. A. aut Akhmetzyanova, E. R. aut Rizvanov, A. A. aut Enthalten in BioNanoScience New York, NY [u.a.] : Springer, 2011 7(2017), 4 vom: 08. Aug., Seite 608-612 (DE-627)657588601 (DE-600)2606470-4 2191-1649 nnns volume:7 year:2017 number:4 day:08 month:08 pages:608-612 https://dx.doi.org/10.1007/s12668-017-0440-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2017 4 08 08 608-612 |
| spelling |
10.1007/s12668-017-0440-0 doi (DE-627)SPR026910977 (SPR)s12668-017-0440-0-e DE-627 ger DE-627 rakwb eng Mukhamedshina, Y. O. verfasserin aut Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC 2017 Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 Zakirova, E. Yu. aut Galieva, L. R. aut Kostennikov, A. A. aut Akhmetzyanova, E. R. aut Rizvanov, A. A. aut Enthalten in BioNanoScience New York, NY [u.a.] : Springer, 2011 7(2017), 4 vom: 08. Aug., Seite 608-612 (DE-627)657588601 (DE-600)2606470-4 2191-1649 nnns volume:7 year:2017 number:4 day:08 month:08 pages:608-612 https://dx.doi.org/10.1007/s12668-017-0440-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2017 4 08 08 608-612 |
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10.1007/s12668-017-0440-0 doi (DE-627)SPR026910977 (SPR)s12668-017-0440-0-e DE-627 ger DE-627 rakwb eng Mukhamedshina, Y. O. verfasserin aut Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC 2017 Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 Zakirova, E. Yu. aut Galieva, L. R. aut Kostennikov, A. A. aut Akhmetzyanova, E. R. aut Rizvanov, A. A. aut Enthalten in BioNanoScience New York, NY [u.a.] : Springer, 2011 7(2017), 4 vom: 08. Aug., Seite 608-612 (DE-627)657588601 (DE-600)2606470-4 2191-1649 nnns volume:7 year:2017 number:4 day:08 month:08 pages:608-612 https://dx.doi.org/10.1007/s12668-017-0440-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2017 4 08 08 608-612 |
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10.1007/s12668-017-0440-0 doi (DE-627)SPR026910977 (SPR)s12668-017-0440-0-e DE-627 ger DE-627 rakwb eng Mukhamedshina, Y. O. verfasserin aut Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC 2017 Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 Zakirova, E. Yu. aut Galieva, L. R. aut Kostennikov, A. A. aut Akhmetzyanova, E. R. aut Rizvanov, A. A. aut Enthalten in BioNanoScience New York, NY [u.a.] : Springer, 2011 7(2017), 4 vom: 08. Aug., Seite 608-612 (DE-627)657588601 (DE-600)2606470-4 2191-1649 nnns volume:7 year:2017 number:4 day:08 month:08 pages:608-612 https://dx.doi.org/10.1007/s12668-017-0440-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2017 4 08 08 608-612 |
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10.1007/s12668-017-0440-0 doi (DE-627)SPR026910977 (SPR)s12668-017-0440-0-e DE-627 ger DE-627 rakwb eng Mukhamedshina, Y. O. verfasserin aut Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media, LLC 2017 Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 Zakirova, E. Yu. aut Galieva, L. R. aut Kostennikov, A. A. aut Akhmetzyanova, E. R. aut Rizvanov, A. A. aut Enthalten in BioNanoScience New York, NY [u.a.] : Springer, 2011 7(2017), 4 vom: 08. Aug., Seite 608-612 (DE-627)657588601 (DE-600)2606470-4 2191-1649 nnns volume:7 year:2017 number:4 day:08 month:08 pages:608-612 https://dx.doi.org/10.1007/s12668-017-0440-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2017 4 08 08 608-612 |
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Mukhamedshina, Y. O. @@aut@@ Zakirova, E. Yu. @@aut@@ Galieva, L. R. @@aut@@ Kostennikov, A. A. @@aut@@ Akhmetzyanova, E. R. @@aut@@ Rizvanov, A. A. @@aut@@ |
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Mukhamedshina, Y. O. |
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Mukhamedshina, Y. O. misc Adipose-derived mesenchymal stem cells misc Spinal cord injury misc Migration Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury |
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Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury Adipose-derived mesenchymal stem cells (dpeaa)DE-He213 Spinal cord injury (dpeaa)DE-He213 Migration (dpeaa)DE-He213 |
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Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury |
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Mukhamedshina, Y. O. Zakirova, E. Yu. Galieva, L. R. Kostennikov, A. A. Akhmetzyanova, E. R. Rizvanov, A. A. |
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distribution and survival of transplanted adipose-derived mesenchymal stem cells in the spinal cord injury |
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Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury |
| abstract |
Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. © Springer Science+Business Media, LLC 2017 |
| abstractGer |
Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. © Springer Science+Business Media, LLC 2017 |
| abstract_unstemmed |
Abstract Current expectations for successful treatment of post-traumatic disorders in the CNS are associated with cell-based technologies. Mesenchymal stem cells, which are under intensive study, appear to be the most promising. At the same time, mechanisms of their effect on post-traumatic regeneration of the spinal cord and their behavior and migration properties in neurodegenerative lesions are not investigated in full. In our study, we investigated the survival, migration, and phenotypic characteristics of a fibrin matrix enclosed in adipose-derived mesenchymal stem cells (AD-MSCs) by implanting them in an area of the spinal cord injury in a subacute period. We showed that adipose-derived mesenchymal stem cells retain their viability in the area of SCI for up to 60 days and migrate rostrally and caudally for more than 5 mm. Phenotyping of AD-MSCs in the spinal cord injury area performed on the seventh day post-transplantation shows that Thy-1, CD 73, and Stro-1 are expressed; however, no CD 44 expression is observed. The results obtained reveal the route of migration of AD-MSCs within an area of the spinal cord injury. However, the programed differentiation of these cells in a later post SCI period has to be studied. © Springer Science+Business Media, LLC 2017 |
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Distribution and Survival of Transplanted Adipose-Derived Mesenchymal Stem Cells in the Spinal Cord Injury |
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https://dx.doi.org/10.1007/s12668-017-0440-0 |
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Zakirova, E. Yu Galieva, L. R. Kostennikov, A. A. Akhmetzyanova, E. R. Rizvanov, A. A. |
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Zakirova, E. Yu Galieva, L. R. Kostennikov, A. A. Akhmetzyanova, E. R. Rizvanov, A. A. |
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10.1007/s12668-017-0440-0 |
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2024-07-03T23:24:19.832Z |
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| score |
7.4010277 |