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 inNeural regeneration research Vol. 12; no. 3; pp. 433 - 439
Main Authors Chen, Tao, Yu, Yan, Tang, Liu-jiu, Kong, Li, Zhang, Cheng-hong, Chu, Hai-ying, Yin, Liang-wei, Ma, Hai-ying
Format Journal Article
LanguageEnglish
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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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.
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.
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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