Neural stem cells over-expressing brain-derived neurotrophic factor promote neuronal survival and cytoskeletal protein expression in traumatic brain injury sites
Cytoskeletal proteins are involved in neuronal survival.Brain-derived neurotrophic factor can increase expression of cytoskeletal proteins during regeneration after axonal injury.However,the effect of neural stem cells genetically modified by brain-derived neurotrophic factor transplantation on neur...
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Published in | Neural regeneration research Vol. 12; no. 3; pp. 433 - 439 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
India
Medknow Publications and Media Pvt. Ltd
01.03.2017
Medknow Publications & Media Pvt. Ltd Department of Neurosurgery,the First Affiliated Hospital of Dalian Medical University,Dalian,Liaoning Province,China%Department of Histology and Embryology,Dalian Medical University,Dalian,Liaoning Province,China 3 Department of Oncology,Dalian Central Hospital,Dalian,Liaoning Province,China%Department of Oncology,Dalian Central Hospital,Dalian,Liaoning Province,China Medknow Publications & Media Pvt Ltd Wolters Kluwer Medknow Publications |
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Online Access | Get full text |
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Summary: | Cytoskeletal proteins are involved in neuronal survival.Brain-derived neurotrophic factor can increase expression of cytoskeletal proteins during regeneration after axonal injury.However,the effect of neural stem cells genetically modified by brain-derived neurotrophic factor transplantation on neuronal survival in the injury site still remains unclear.To examine this,we established a rat model of traumatic brain injury by controlled cortical impact.At 72 hours after injury,2 × 10~7 cells/m L neural stem cells overexpressing brain-derived neurotrophic factor or naive neural stem cells(3 m L) were injected into the injured cortex.At 1–3 weeks after transplantation,expression of neurofilament 200,microtubule-associated protein 2,actin,calmodulin,and beta-catenin were remarkably increased in the injury sites.These findings confirm that brain-derived neurotrophic factor-transfected neural stem cells contribute to neuronal survival,growth,and differentiation in the injury sites.The underlying mechanisms may be associated with increased expression of cytoskeletal proteins and the Wnt/β-catenin signaling pathway. |
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Bibliography: | nerve regeneration; brain-derived neurotrophic factor; neural stem cells; transfect; differentiation; traumatic brain injury; cytoskeleton;neurofilament; microtubule-associated proteins; calmodulin; Wnt/β-catenin; neural regeneration Cytoskeletal proteins are involved in neuronal survival.Brain-derived neurotrophic factor can increase expression of cytoskeletal proteins during regeneration after axonal injury.However,the effect of neural stem cells genetically modified by brain-derived neurotrophic factor transplantation on neuronal survival in the injury site still remains unclear.To examine this,we established a rat model of traumatic brain injury by controlled cortical impact.At 72 hours after injury,2 × 10~7 cells/m L neural stem cells overexpressing brain-derived neurotrophic factor or naive neural stem cells(3 m L) were injected into the injured cortex.At 1–3 weeks after transplantation,expression of neurofilament 200,microtubule-associated protein 2,actin,calmodulin,and beta-catenin were remarkably increased in the injury sites.These findings confirm that brain-derived neurotrophic factor-transfected neural stem cells contribute to neuronal survival,growth,and differentiation in the injury sites.The underlying mechanisms may be associated with increased expression of cytoskeletal proteins and the Wnt/β-catenin signaling pathway. 11-5422/R ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Author contributions: TC and YY conceived and designed the study, analyzed data and wrote the paper. LJT and HYC participated in cell culture, immunofluorescence and western blot assay. LK provided reference data and technical support. CHZ participated in cell culture and TBI model establishment. LWY participated in transplantation, ensured the integrity of the data and obtained the funding. HYM served as a principle investigator, obtained the funding, conceived and designed the study. All authors approved the final version of the paper. |
ISSN: | 1673-5374 1876-7958 |
DOI: | 10.4103/1673-5374.202947 |