Literature DB >> 10719896

Functional recovery of paraplegic rats and motor axon regeneration in their spinal cords by olfactory ensheathing glia.

A Ramón-Cueto1, M I Cordero, F F Santos-Benito, J Avila.   

Abstract

Axonal regeneration in the lesioned mammalian central nervous system is abortive, and this causes permanent disabilities in individuals with spinal cord injuries. In adult rats, olfactory ensheathing glia (OEG) transplants successfully led to functional and structural recovery after complete spinal cord transection. From 3 to 7 months post surgery, all OEG-transplanted animals recovered locomotor functions and sensorimotor reflexes. They presented voluntary hindlimb movements, they supported their body weight, and their hindlimbs responded to light skin contact and proprioceptive stimuli. In addition, relevant motor axons (corticospinal, raphespinal, and coeruleospinal) regenerated for long distances within caudal cord stumps. Therefore, OEG transplantation provides a useful repair strategy in adult mammals with traumatic spinal cord injuries. Our results with these cells could lead to new therapies for the treatment of spinal cord lesions in humans.

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Mesh:

Year:  2000        PMID: 10719896     DOI: 10.1016/s0896-6273(00)80905-8

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  164 in total

Review 1.  Could enhanced reflex function contribute to improving locomotion after spinal cord repair?

Authors:  K G Pearson
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

Review 2.  Neural prostheses.

Authors:  A Prochazka; V K Mushahwar; D B McCreery
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

3.  Locomotor recovery in spinal cord-injured rats treated with an antibody neutralizing the myelin-associated neurite growth inhibitor Nogo-A.

Authors:  D Merkler; G A Metz; O Raineteau; V Dietz; M E Schwab; K Fouad
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

Review 4.  Stem cell and precursor cell therapy.

Authors:  Jingli Cai; Mahendra S Rao
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 3.843

5.  Further evidence of olfactory ensheathing glia facilitating axonal regeneration after a complete spinal cord transection.

Authors:  Matthias D Ziegler; Derek Hsu; Aya Takeoka; Hui Zhong; Almudena Ramón-Cueto; Patricia E Phelps; Roland R Roy; V Reggie Edgerton
Journal:  Exp Neurol       Date:  2011-01-25       Impact factor: 5.330

Review 6.  Strategies for identifying genes that play a role in spinal cord regeneration.

Authors:  M Wintzer; M Mladinic; D Lazarevic; C Casseler; A Cattaneo; J Nicholls
Journal:  J Anat       Date:  2004-01       Impact factor: 2.610

7.  LacZ-expressing olfactory ensheathing cells do not associate with myelinated axons after implantation into the compressed spinal cord.

Authors:  J G Boyd; J Lee; V Skihar; R Doucette; M D Kawaja
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-05       Impact factor: 11.205

8.  Transplantation of olfactory ensheathing cells into spinal cord lesions restores breathing and climbing.

Authors:  Ying Li; Patrick Decherchi; Geoffrey Raisman
Journal:  J Neurosci       Date:  2003-02-01       Impact factor: 6.167

9.  Identified olfactory ensheathing cells transplanted into the transected dorsal funiculus bridge the lesion and form myelin.

Authors:  Masanori Sasaki; Karen L Lankford; Micheas Zemedkun; Jeffery D Kocsis
Journal:  J Neurosci       Date:  2004-09-29       Impact factor: 6.167

10.  Graft of a tissue-engineered neural scaffold serves as a promising strategy to restore myelination after rat spinal cord transection.

Authors:  Bi-Qin Lai; Jun-Mei Wang; Eng-Ang Ling; Jin-Lang Wu; Yuan-Shan Zeng
Journal:  Stem Cells Dev       Date:  2014-02-06       Impact factor: 3.272

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