Therapeutic Potential of a Combination of Electroacupuncture and TrkB-Expressing Mesenchymal Stem Cells for Ischemic Stroke

Mol Neurobiol. 2019 Jan;56(1):157-173. doi: 10.1007/s12035-018-1067-z. Epub 2018 Apr 22.

Abstract

We prepared and grafted tropomyosin receptor kinase B (TrkB) gene-transfected mesenchymal stem cells (TrkB-MSCs) into the ischemic penumbra and investigated whether electroacupuncture (EA) treatment could promote functional recovery from ischemic stroke. For the behavioral test, TrkB-MSCs+EA resulted in significantly improved motor function compared to that obtained with MSCs+EA or TrkB-MSCs alone. At 30 days after middle cerebral artery occlusion (MCAO), the largest number of grafted MSCs was detected in the TrkB-MSC+EA group. Some differentiation into immature neuroblasts and astrocytes was detected; however, only a few mature neuron-like cells were found. Compared to other treatments, TrkB-MSCs+EA upregulated the expression of mature brain-derived neurotrophic factor (BDNF) and neurotrophin-4/5 (NT4) and induced the activation of TrkB receptor and its transcription factor cAMP response element-binding protein (CREB). At 60 days after MCAO, EA highly promoted the differentiation of TrkB-MSCs into mature neuron-like cells compared to the effect in MSCs. A selective TrkB antagonist, ANA-12, reverted the effect of TrkB-MSCs+EA in motor function recovery and survival of grafted MSCs. Our results suggest that EA combined with grafted TrkB-MSCs promotes the expression of BDNF and NT4, induces the differentiation of TrkB-MSCs, and improves motor function. TrkB-MSCs could serve as effective therapeutic agents for ischemic stroke if used in combination with BDNF/NT4-inducing therapeutic approaches.

Keywords: Brain-derived neurotrophic factor; Electroacupuncture; Ischemic stroke; Mesenchymal stem cells; Neurotrophin-4; Tropomyosin receptor kinase B.

MeSH terms

  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism
  • Astrocytes / pathology
  • Azepines / pharmacology
  • Benzamides / pharmacology
  • Brain Ischemia / genetics
  • Brain Ischemia / pathology
  • Brain Ischemia / physiopathology
  • Brain Ischemia / therapy*
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cell Differentiation / drug effects
  • Cell Survival / drug effects
  • Combined Modality Therapy
  • Electroacupuncture*
  • Gene Expression Regulation / drug effects
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism*
  • Mice, Inbred C57BL
  • Motor Activity / drug effects
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • Neurons / pathology
  • Receptor, trkB / metabolism*
  • Signal Transduction / drug effects
  • Stroke / genetics
  • Stroke / pathology
  • Stroke / physiopathology
  • Stroke / therapy*

Substances

  • ANA 12 compound
  • Azepines
  • Benzamides
  • Brain-Derived Neurotrophic Factor
  • Nerve Growth Factors
  • Receptor, trkB
  • neurotrophin 4