Co-culturing improves the OGD-injured neuron repairing and NSCs differentiation via Notch pathway activation.

Neurosci Lett

Department of Neurology, Jinling Hospital, Nanjing University School of Medicine, 305 East Zhongshan Road, Nanjing 210002, Jiangsu, China. Electronic address:

Published: January 2014

AI Article Synopsis

  • The study explores how neural stem cell (NSC) transplantation can repair neuronal injury from ischemic stroke by creating an environment that encourages communication between injured neurons and transplanted NSCs.
  • An in vitro co-culturing system was developed with oxygen-glucose deprivation (OGD) injured neurons and NSCs to assess their interaction, focusing on the activation of the Notch1 pathway as a key player in this process.
  • Results indicated that OGD-injured neurons enhanced Notch1 activation in NSCs, promoting their differentiation and neurotrophic effects; inhibiting the Notch pathway reduced these beneficial effects, demonstrating the importance of Notch1 in neuronal repair mechanisms.

Article Abstract

Neural stem cell (NSC) transplantation for ischemic stroke is expected to repair the neuronal injury and replace the lost neurons through cell-cell cross talk between injured neurons and the transplanted NSCs. Here, we set up an in vitro co-culturing system of oxygen-glucose deprivation (OGD) injured neurons and NSCs to investigate the neuronal repairing effect and effects on NSCs differentiation. We focused on the Notch1 pathway as a possible mediator of these effects. OGD-injured neurons induced increased activation of Notch1 in co-cultured NSCs, through the up-regulations of the DLL1, the Notch1 intracellular domain (NICD) and the down-stream genes Hes1/5. When the NSCs were pre-treated with the Notch pathway inhibitor DAPT, the activation of Notch1 was blocked, lower NSCs differentiation was detected and the neurotrophic effect was also abolished. As shown by the novel co-culturing system, the NSCs co-cultured with OGD injured neurons were induced to differentiate through the Notch1 pathway activation; and these induced NSCs showed greater potential to support both the repair of injured neurons and form new neurons.

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Source
http://dx.doi.org/10.1016/j.neulet.2013.11.027DOI Listing

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