Literature DB >> 16629629

Schwann cell transplantation for repair of the adult spinal cord.

Martin Oudega1, Xiao-Ming Xu.   

Abstract

The Schwann cell is one of the most widely studied cell types for repair of the spinal cord. These cells play a crucial role in endogenous repair of peripheral nerves due to their ability to dedifferentiate, migrate, proliferate, express growth promoting factors, and myelinate regenerating axons. Following trauma to the spinal cord, Schwann cells migrate from the periphery into the injury site, where they apparently participate in endogenous repair processes. For transplantation into the spinal cord, large numbers of Schwann cells are necessary to fill injury-induced cystic cavities. Several culture systems have been developed that provide large, highly purified populations of Schwann cells. Importantly, the development of in vitro systems to harvest human Schwann cells presents a unique opportunity for autologous transplantation in the clinic. In animal models of spinal cord injury (SCI), grafting Schwann cells or peripheral nerve into the lesion site has been shown to promote axonal regeneration and myelination. However, axons do not regenerate beyond the transplant due to the inhibitory nature of the glial scar surrounding the injury. To overcome the glial scar inhibition, additional approaches such as increasing the intrinsic capacity of axons to regenerate and/or removal of the inhibitory molecules associated with reactive astrocytes and/or oligodendrocyte myelin should be incorporated. Clearly, Schwann cells have great potential for repair of the injured spinal cord, but they need to be combined with other interventions to maximize axonal regeneration and functional recovery.

Entities:  

Mesh:

Year:  2006        PMID: 16629629     DOI: 10.1089/neu.2006.23.453

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  64 in total

Review 1.  Recent therapeutic strategies for spinal cord injury treatment: possible role of stem cells.

Authors:  D Garbossa; M Boido; M Fontanella; C Fronda; A Ducati; A Vercelli
Journal:  Neurosurg Rev       Date:  2012-04-27       Impact factor: 3.042

2.  Aspiration of a cervical spinal contusion injury in preparation for delayed peripheral nerve grafting does not impair forelimb behavior or axon regeneration.

Authors:  Harra R Sandrow; Jed S Shumsky; Arthi Amin; John D Houle
Journal:  Exp Neurol       Date:  2007-12-15       Impact factor: 5.330

3.  Transduced Schwann cells promote axon growth and myelination after spinal cord injury.

Authors:  Kevin L Golden; Damien D Pearse; Bas Blits; Maneesh S Garg; Martin Oudega; Patrick M Wood; Mary Bartlett Bunge
Journal:  Exp Neurol       Date:  2007-07-13       Impact factor: 5.330

4.  Combined effects of rat Schwann cells and 17β-estradiol in a spinal cord injury model.

Authors:  Zeinab Namjoo; Fateme Moradi; Roya Aryanpour; Abbas Piryaei; Mohammad Taghi Joghataei; Yusef Abbasi; Amir Hosseini; Sajad Hassanzadeh; Fatemeh Ranjbar Taklimie; Cordian Beyer; Adib Zendedel
Journal:  Metab Brain Dis       Date:  2018-04-15       Impact factor: 3.584

Review 5.  Novel combination strategies to repair the injured mammalian spinal cord.

Authors:  Mary Bartlett Bunge
Journal:  J Spinal Cord Med       Date:  2008       Impact factor: 1.985

6.  A guidance channel seeded with autologous Schwann cells for repair of cauda equina injury in a primate model.

Authors:  Blair Calancie; Parley W Madsen; Patrick Wood; Alexander E Marcillo; Allan D Levi; Richard P Bunge
Journal:  J Spinal Cord Med       Date:  2009       Impact factor: 1.985

7.  Cell Therapy From Bench to Bedside Translation in CNS Neurorestoratology Era.

Authors:  Hongyun Huang; Lin Chen; Paul Sanberg
Journal:  Cell Med       Date:  2010-01-01

Review 8.  Peripheral nerve grafts support regeneration after spinal cord injury.

Authors:  Marie-Pascale Côté; Arthi A Amin; Veronica J Tom; John D Houle
Journal:  Neurotherapeutics       Date:  2011-04       Impact factor: 7.620

9.  GDNF-enhanced axonal regeneration and myelination following spinal cord injury is mediated by primary effects on neurons.

Authors:  Liqun Zhang; Zhengwen Ma; George M Smith; Xuejun Wen; Yelena Pressman; Patrick M Wood; Xiao-Ming Xu
Journal:  Glia       Date:  2009-08-15       Impact factor: 7.452

10.  Oligodendrocyte precursor cells differentially expressing Nogo-A but not MAG are more permissive to neurite outgrowth than mature oligodendrocytes.

Authors:  Zhengwen Ma; Qilin Cao; Liqun Zhang; Jianguo Hu; Russell M Howard; Peihua Lu; Scott R Whittemore; Xiao-Ming Xu
Journal:  Exp Neurol       Date:  2009-02-21       Impact factor: 5.330

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