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|Title:||Effect of the combined lithium and noggin treatment on the responses of neural progenitor cells and functional recovery after chronic spinal cord injury in adult mice|
|Authors:||Dai, Y;Pan, Y;Yip, HKF|
|subject:||Spinal Cord Injury;Endogenous Neural Stem Cells;Functional Recovery|
|Publisher:||Society for Neuroscience. The Journal's web site is located at http://www.elsevier.com/locate/neuroscience|
|Description:||Topic: D.10. Spinal Cord Injury and Plasticity|
Fulltext of the abstract in: http://www.abstractsonline.com/plan/ViewAbstract.aspx?cKey=a385ab6a-2768-46b1-9f79-e96584015850&mID=3236&mKey=8d2a5bec-4825-4cd6-9439-b42bb151d1cf&sKey=0b785a85-b44d-45a8-92fc-6901ff7482ca
Background: p300 transcription factor is found to bridge the STAT-Smad complex signaling. It is possible that the combinatory approach of LiCl and Noggin enables concomitant suppression of glial scarring and reactivation of neurogensis and remyelination, which leads to functional recovery after chronic spinal cord injury (SCI). Objectives: To examine whether LiCl and/or noggin can modulate the proliferation and differentiation of neural progenitor cells (NPCs) in the injured adult mouse spinal cord (SC), and to examine the effect of the combined treatment on the scar formation, promotion of axonal regeneration and functional recovery in the chronically injured adult SC. Methods: Thoracic SC segment (T8-T10) of 4-6-week-old C57/Bl6n mice were exposed after laminectomy and subjected to a contusion injury with a force of 37.5 kdyne. T8-T10 SC segments were dissected from the mice 24 h after contusion injury and prepared for neurosphere culture. Passaged neurosphere cells were grown in differentiation medium with the addition of LiCl (0.5mM-2mM) or noggin (7.5ng/ml-30ng/ml) alone, or a combination of LiCl (1mM) and noggin (15ng/ml) for 7 days. Neurosphere cells were treated with LiCl ± noggin for 4 days before BrdU labeling. Four weeks after the contusion injury, osmotic minipumps delivering treatments (LiCl ± noggin) and vehicle were implanted onto the injured mice for 2 weeks. BMS test was conducted to examine the recovery of locomotor movement 2 hours before the mice were sacrificed. SC tissue 5mm rostral and caudal apart from the injury epicenter was collected for immunostaining. Results: 1mM of LiCl or 15ng/ml of noggin alone has a maximal effect in promoting both NPC proliferation and differentiation of neurons and oligodendrocytes, while at the same time decreasing astrogenesis. Combined treatment of LiCl and noggin demonstrated a synergistic effect on promoting NPC differentiation along neuronal and oligodendroglial lineage. Combined LiCl and noggin treatment increased the number of immature neurons, mature neurons, oligodendrocyte precursors and oligodendrocytes while decreased the number of astrocytes and microglial cells after chronic SCI. The chronically injured mice treated with combined LiCl and noggin demonstrated significantly better locomotor movement recovery. Conclusion: LiCl and noggin promoted neuronal and oligodendroglial differentiation of adult SC-derived NPCs and at the same time inhibited astroglia differentiation. Combined LiCl and noggin treatment has a synergistic effect on the functional recovery of chronic adult SCI. The mechanism of the synergistic effect is currently under investigation.
|Standard no:||The 43rd Annual Meeting of the Society for Neuroscience (SfN), San Diego, California, USA, 9-13 November 2013|
|Appears in Collections:||Department of Anatomy|
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