| Literature DB >> 28719819 |
Paul M George1, Tonya M Bliss2, Thuy Hua2, Alex Lee3, Byeongtaek Oh4, Alexa Levinson4, Swapnil Mehta5, Guohua Sun2, Gary K Steinberg6.
Abstract
Exogenous human neural progenitor cells (hNPCs) are promising stroke therapeutics, but optimal delivery conditions and exact recovery mechanisms remain elusive. To further elucidate repair processes and improve stroke outcomes, we developed an electrically conductive, polymer scaffold for hNPC delivery. Electrical stimulation of hNPCs alters their transcriptome including changes to the VEGF-A pathway and genes involved in cell survival, inflammatory response, and synaptic remodeling. In our experiments, exogenous hNPCs were electrically stimulated (electrically preconditioned) via the scaffold 1 day prior to implantation. After in vitro stimulation, hNPCs on the scaffold are transplanted intracranially in a distal middle cerebral artery occlusion rat model. Electrically preconditioned hNPCs improved functional outcomes compared to unstimulated hNPCs or hNPCs where VEGF-A was blocked during in vitro electrical preconditioning. The ability to manipulate hNPCs via a conductive scaffold creates a new approach to optimize stem cell-based therapy and determine which factors (such as VEGF-A) are essential for stroke recovery.Entities:
Keywords: Cell transplantation; Conductive polymer; Electrical stimulation; Neural stem cell; Stroke recovery; Tissue engineering
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Year: 2017 PMID: 28719819 PMCID: PMC5575756 DOI: 10.1016/j.biomaterials.2017.07.020
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 15.304