Literature DB >> 12429228

Transplants of fibroblasts genetically modified to express BDNF promote axonal regeneration from supraspinal neurons following chronic spinal cord injury.

Ying Jin1, Itzhak Fischer, Alan Tessler, John D Houle.   

Abstract

Transplants of fibroblasts genetically modified to express BDNF (Fb/BDNF) have been shown to promote regeneration of rubrospinal axons and recovery of forelimb function when placed acutely into the injured cervical spinal cord of adult rats. Here we investigated whether Fb/BDNF cells could stimulate supraspinal axon regeneration and recovery after chronic (4 week) injury. Adult female Sprague-Dawley rats received a complete unilateral hemisection injury at the third cervical spinal cord segment (C3). Four-five weeks later the injury site was exposed and rats received transplants of unmodified fibroblasts (Fb/UM) or Fb/BDNF. Four-five weeks after transplantation, locomotor recovery was examined on a test of forelimb usage and regeneration of supraspinal axons was studied following injection of the anterograde tracer biotin dextran amine (BDA). Rubrospinal tract (RST), reticulospinal tract (ReST), and vestibulospinal tract (VST) axons regenerated into transplants of either Fb/UM or Fb/BDNF but the length of axonal growth was significantly different in the two groups. The absolute distance of ReST growth was 1.8-fold greater in Fb/BDNF than in Fb/UM and the absolute distance of growth of RST and VST axons showed a statistically significant 4-fold increase. All three types of regenerated axons occupied a greater proportional length of Fb/BDNF transplants than of Fb/UM transplants. Only VST axons extended into the host spinal cord caudal to the Fb/BDNF grafts, but these axons were sparse. Rats receiving Fb/BDNF used both forelimbs together to explore walls of a cylinder more often than rats receiving Fb/UM, indicating partial recovery of forelimb usage. These results demonstrate that fibroblasts genetically modified to express BDNF promote axon regeneration from supraspinal neurons in the chronically injured spinal cord with accompanying partial recovery of locomotor performance.

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Year:  2002        PMID: 12429228     DOI: 10.1006/exnr.2002.7980

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  60 in total

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4.  Chronic enhancement of the intrinsic growth capacity of sensory neurons combined with the degradation of inhibitory proteoglycans allows functional regeneration of sensory axons through the dorsal root entry zone in the mammalian spinal cord.

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Review 5.  Gene therapy approaches to enhancing plasticity and regeneration after spinal cord injury.

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Journal:  Exp Neurol       Date:  2011-01-31       Impact factor: 5.330

6.  Axonal regeneration of different tracts following transplants of human glial restricted progenitors into the injured spinal cord in rats.

Authors:  Ying Jin; Jed S Shumsky; Itzhak Fischer
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Review 7.  Growth factors and combinatorial therapies for CNS regeneration.

Authors:  Paul Lu; Mark H Tuszynski
Journal:  Exp Neurol       Date:  2007-08-22       Impact factor: 5.330

8.  A pilot study of poly(N-isopropylacrylamide)-g-polyethylene glycol and poly(N-isopropylacrylamide)-g-methylcellulose branched copolymers as injectable scaffolds for local delivery of neurotrophins and cellular transplants into the injured spinal cord.

Authors:  Lauren Conova; Jennifer Vernengo; Ying Jin; B Timothy Himes; Birgit Neuhuber; Itzhak Fischer; Anthony Lowman; Jennifer Vernengo; Ying Jin; B Timothy Himes; Birgit Neuhuber; Itzhak Fischer; Anthony Lowman
Journal:  J Neurosurg Spine       Date:  2011-09-02

9.  Preferential and bidirectional labeling of the rubrospinal tract with adenovirus-GFP for monitoring normal and injured axons.

Authors:  Xiaofei Wang; George M Smith; Xiao-Ming Xu
Journal:  J Neurotrauma       Date:  2011-03-24       Impact factor: 5.269

10.  Controlled release of neurotrophin-3 from fibrin-based tissue engineering scaffolds enhances neural fiber sprouting following subacute spinal cord injury.

Authors:  Philip J Johnson; Stanley R Parker; Shelly E Sakiyama-Elbert
Journal:  Biotechnol Bioeng       Date:  2009-12-15       Impact factor: 4.530

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