Literature DB >> 11811255

Transplantation of genetically modified fibroblasts expressing BDNF in adult rats with a subtotal hemisection improves specific motor and sensory functions.

D Kim1, T Schallert, Y Liu, T Browarak, N Nayeri, A Tessler, M Murray.   

Abstract

OBJECTIVE: We have previously reported that grafting fibroblasts genetically modified to express brain-derived neurotrophic factor (BDNF) into a subtotal cervical hemisection site that destroys the entire lateral funiculus will promote regeneration of rubrospinal axons and growth of other axons, prevent atrophy and death of axotomized red nucleus neurons, and improve forelimb use during spontaneous vertical exploration. We have now extended these studies by using additional sensorimotor tests to examine recovery.
METHODS: The range of tests used included those in which the intervention did not improve recovery, those in which the intervention was associated with recovery, and those that showed little deficit. The selected tasks tested both sensory and motor functions and both forelimb and forelimb function. We used the open-field locomotor rating scale (BBB), locomotion on a narrow beam, forelimb use during swimming, horizontal rope walking, and a somatosensory asymmetry (patch-removal) test. After testing during an 8-week recovery period, a second lesion was made just rostral to the initial lesion/transplant site to test the role of the transplant in recovery. The rats were then retested for a further 5 weeks after the repeated lesion.
RESULTS: The horizontal rope, swim, and patch-removal tests were reliably sensitive to the subtotal hemisection injury. Fb/BDNF-transplanted animals recovered motor functions on the horizontal rope-crossing test, and this recovery was abolished by a second lesion just rostral to the first lesion/transplant. In the patch-removal test, the latency to contact the affected limb was shorter in Fb/BDNF-treated rats than in the control group, and this effect was completely abolished by a second lesion.
CONCLUSIONS: The rope-crossing and patch-removal tests are particularly useful tasks for assessing the beneficial effects of BDNF-expressing grafts in this injury model.

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Year:  2001        PMID: 11811255     DOI: 10.1177/154596830101500207

Source DB:  PubMed          Journal:  Neurorehabil Neural Repair        ISSN: 1545-9683            Impact factor:   3.919


  12 in total

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2.  Apparent diffusion coefficients in spinal cord transplants and surrounding white matter correlate with degree of axonal dieback after injury in rats.

Authors:  Eric D Schwartz; Chih-Liang Chin; Jed S Shumsky; Abbas F Jawad; B Kooper Brown; Suzanne Wehrli; Alan Tessler; Marion Murray; David B Hackney
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3.  MicroRNA-185 regulates spinal cord injuries induced by thoracolumbar spine compression fractures by targeting transforming growth factor-β1.

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4.  Combinatorial therapy with neurotrophins and cAMP promotes axonal regeneration beyond sites of spinal cord injury.

Authors:  Paul Lu; Hong Yang; Leonard L Jones; Marie T Filbin; Mark H Tuszynski
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5.  Targeting a dominant negative rho kinase to neurons promotes axonal outgrowth and partial functional recovery after rat rubrospinal tract lesion.

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6.  Assessing forelimb function after unilateral cervical SCI using novel tasks: limb step-alternation, postural instability and pasta handling.

Authors:  Zin Z Khaing; Sydney A Geissler; Timothy Schallert; Christine E Schmidt
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7.  Bidirectional remodeling of β1-integrin adhesions during chemotropic regulation of nerve growth.

Authors:  Lucas P Carlstrom; Jacob H Hines; Steven J Henle; John R Henley
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Review 8.  Biomaterials as carrier, barrier and reactor for cell-based regenerative medicine.

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Review 9.  The role of the serotonergic system in locomotor recovery after spinal cord injury.

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10.  Rodent Models and Behavioral Outcomes of Cervical Spinal Cord Injury.

Authors:  Sydney A Geissler; Christine E Schmidt; Timothy Schallert
Journal:  J Spine       Date:  2013-07-27
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