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. 2020 Apr 29;21(9):3135. doi: 10.3390/ijms21093135

Table 2.

Summary of therapeutic effects of combining cell therapy and brain stimulation on motor function in animal models.

Reference Model Cell Therapy Rehabilitation Outcome
Transplanted Cell Cell Mass and Location Timing of Transplantation Category Onset Duration Interactive Effect on Motor Function Mechanism
Kremer et al. [91]
(2016)
Normal rats Human dental pulp stem cells 6 × 105 cells, right cortex and striatum n.a. Ipsilateral TMS
(60% of the maximal output, 0.2 Hz for 15 min, every 2nd day, beginning on day 3 post-transplantation)
2 days after transplantation 12 days Antagonistic ↓Transplanted cell survival
↑Apoptosis
Morimoto et al. [89]
(2018)
MCAO in rats rMSCs 2.5 × 105 cells, contralateral corpus callosum 1 day after MCAO Ipsilesional cathodal CS
(100 µA, 100 Hz, continuously)
1 day after MCAO 14 days n.a. ↓Infarction volume
↑Transplanted cell migration
↑SDF-1α
Peng et al. [92]
(2019)
MCAO in rats hNSCs 2.5 × 105 cells, ipsilateral striatum 4 days after MCAO Ipsilesional rTMS
(26% of the maximal output, 10 Hz, 300 pulses/day, every day)
5 days after MCAO 28 days Synergistic ↑Neurogenesis in SVZ
↑BDNF/TrkB signaling pathway
↑Neural differentiation

TMS: transcranial magnetic stimulation; MCAO: middle cerebral artery occlusion; rMSCs: rat mesenchymal stem cells; CS: epidural cortical stimulation; SDF-1α: stromal cell-derived factor-1α; hNSCs: human neural stem cells; rTMS: repetitive transcranial magnetic stimulation; SVZ: subventricular zone; BDNF: brain-derived neurotrophic factor; TrkB: tropomyosin receptor kinase B; ↑: up-regulation; ↓: down-regulation.