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Inicio Revista Española de Cirugía Ortopédica y Traumatología El trasplante de células de la glía envolvente del bulbo olfatorio tras lesió...
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Vol. 49. Núm. 4.
Páginas 301-306 (enero 2004)
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Vol. 49. Núm. 4.
Páginas 301-306 (enero 2004)
Acceso a texto completo
El trasplante de células de la glía envolvente del bulbo olfatorio tras lesión de la médula espinal: Estudio experimental en ratas
Transplantation of olfactory bulb ensheathing glia after spinal cord injury: experimental study in rats
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G. García-Alíasa, R. López-Valesa, E. Verdúa, X. Navarroa, S. Susob, J. Forésa,b,
Autor para correspondencia
jfores@clinic.ub.es

Correspondencia: Universidad de Barcelona. Instituto del Aparato Locomotor. Unidad de la mano y del sistema nervioso periférico. Hospital Clínico y Provincial . C/ Villarroel, 170 08036 Barcelona.
a Grupo de Neuroplasticidad y Regeneración. Universidad Autónoma de Barcelona. Instituto de Neurociencias. Departamentos de Biología Celular, Fisiología e Inmunología. Facultad de Medicina. Bellaterra
b Instituto del Aparato Locomotor. Universidad de Barcelona. Unidad de la mano y del sistema nervioso periférico. Hospital Clínico y Provincial. Barcelona
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Estadísticas
Objetivo

Evaluar el efecto a largo plazo del trasplante de celulas de la glia envolvente (GE) del bulbo olfatorio tras lesion de la medula espinal.

Material y método

Se practico una laminectomia dorsal T8, en 16 ratas adultas Sprague-Dawley, dejando al descubierto la medula espinal subyacente, la cual se bano con rosa de Bengala durante 10 minutos, antes de lesionarla por iluminacion con una fibra optica acoplada a una lampara halogena, durante 2,5 minutos. A la mitad de los animales se les inyecto 180.000 celulas de GE, en 10 μl de medio (grupo GE), y a la otra mitad solo 10 μl de DMEM (Dulbecco's modified Eagle's medium) (grupo DM). Los animales se sacrificaron a los 90 dias de efectuar la lesion y se evaluo el area de medula espinal preservada, la recuperacion locomotora y la sensibilidad nociceptiva.

Resultados

Los animales del grupo GE mostraron un nivel de locomocion superior y retiraron antes la pata al estimulo nociceptivo que los del grupo DM. Tambien hubo una mayor preservacion de parenquima medular y mas celulas p75 positivas en el grupo GE que en el DM.

Conclusiones

El trasplante de GE favorece la preservacion de parenquima medular y evita la perdida de funciones motoras y sensoriales en la rata.

Palabras clave:
paraplejía
columna vertebral
algesimetría
glía envolvente
médula espinal
Aim

To evaluate the long-term effect of the transplantation of olfactory bulb ensheathing glia (EG) after spinal cord injury.

Materials and methods

Dorsal laminectomy of T8 was performed in 16 adult Sprague-Dawley rats, exposing the underlying spinal cord, which was bathed with Bengala pink for 10 minutes before producing a lesion by fiberoptic focusing of light from a halogen lamp for 2.5 minutes. Half of the animals were injected 180,000 ensheathing glia (EG) in 10 ìl of medium (EG group) and half were injected only 10 ìl of DMEM (Dulbecco's modified Eagle medium) (DM group). Animals were sacrificed 90 days after injury and the area of spinal cord conserved, locomotor recovery, and nociceptive sensitivity were evaluated.

Results

The animals in the EG group showed better locomotion and quicker paw retraction in response to a nociceptive stimulus than the animals in the DM group. More of the spinal parenchyma was preserved and there were more positive p75 cells in the EG group than in the DM group.

Conclusions

EG transplantation favored the preservation of spinal parenchyma and prevented the loss of motor and sensorial functions in the rat.

Key words:
paraplegia
spine
algesimetry
ensheathing glia
spinal cord
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Bibliografía
[1.]
A.P. Amar, M.L. Levy.
Pathogenesis and pharmacological strategies for mitigating secondary damage in acute spinal cord injury.
Neurosurg, 44 (1999), pp. 1027-1040
[2.]
A.R. Allen.
Surgery of experimental lesions of spinal cord equivalent to crush injury of fracture dislocation of spinal column. A preliminary report.
J Am Med Assoc, 57 (1911), pp. 878-880
[3.]
D.M. Basso, M.S. Beattie, J.C. Bresnahan.
Graded histological and locomotor outcomes after spinal cord contusion using the NYU weight-drop device versus transection.
Exp Neurol, 139 (1996), pp. 244-256
[4.]
R. Prado, W.D. Dietrich, B.D. Watson, M.D. Ginsberg, B.A. Green.
Photochemically induced graded spinal cord infarction.
J Neurosurg, 67 (1987), pp. 745-753
[5.]
A.S. Rivlin, C.H. Tator.
Effect of duration of acute spinal cord compression in a new acute model in the rat.
Surg Neurol, 10 (1978), pp. 38-43
[6.]
E. Verdú, G. García-Alías, J. Forés, J.M. Vela, J. Cuadras, R. López-Vales, et al.
Morphological characterization of photochemical graded spinal cord injury in the rat.
J Neurotrauma, 20 (2003), pp. 483-499
[7.]
M.E. Schwab, D. Bartholdi.
Degeneration and regeneration of axons in the lesioned spinal cord.
Physiol Rev, 76 (1996), pp. 319-370
[8.]
P. Bovolenta, I. Fernaud-Espinosa, R. Méndez-Otero, M. Nieto-Sampedro.
Neurite Outgrowth inhibitor of gliotic brain tissue. Mode of action and cellular localization, studied with specific monoclonal antibodies.
Eur J Neurosci, 9 (1997), pp. 977-989
[9.]
G. Gudiño-Cabrera, M. Nieto-Sampedro.
Schwann-like macroglia in adult rat brain.
Glia, 30 (2000), pp. 49-63
[10.]
G. Gudiño-Cabrera, M. Nieto-Sampedro.
Ensheathing cells: large scale purification from adult olfactory bulb, freeze-preservation and migration of transplanted cells in adult brain.
Restor Neurol Neurosci, 10 (1996), pp. 25-34
[11.]
E. Verdú, G. García-Alías, J. Forés, R. López-Vales, X. Navarro.
Olfactory ensheathing cells transplanted in lesioned spinal cord prevent loss of spinal cord parenchyma and promote functional recovery.
Glia, 42 (2003), pp. 275-286
[12.]
D.M. Basso, M.S. Beattie, J.C. Bresnahan.
A sensitive and reliable locomotor rating scale for open field testing in rats.
J Neurotrauma, 12 (1995), pp. 1-21
[13.]
K. Hargreaves, R. Dubner, F. Brown, C. Flores, J. Joris.
A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia.
Pain, 32 (1988), pp. 77-88
[14.]
E. Verdú, G. García-Alías, J. Forés, G. Gudiño-Cabrera, V.C. Muñetón, M. Nieto-Sampedro, et al.
Effects of ensheathing cells transplanted into photochemically damaged spinal cord.
Neuroreport, 12 (2001), pp. 2303-2309
[15.]
A.V. Boruch, J.J. Conners, M. Pipitone, G. Deadwyler, P.D. Storer, G.H. Devries, et al.
Neurotrophic and migratory properties of an olfactory ensheathing cell line.
Glia, 33 (2001), pp. 225-229
[16.]
T. Imaizumi, K.L. Lankford, J.D. Kocsis.
Transplantation of olfactory ensheathing cells or Schwann cells restores rapid and secure conduction across the transected spinal cord.
Brain Res, 854 (2000), pp. 70-78
[17.]
J. Lu, F. Féron, A. Mackay-Sim, P.M.E. Waite.
Olfactory ensheathing cells promote locomotor recovery after delayed transplantation into transected spinal cord.
Brain, 125 (2002), pp. 14-21
[18.]
A. Ramón-Cueto, M.I. Cordero, F.F. Santos-Benito, J. Ávila.
Functional recovery of paraplegic rats and motor axon regeneration in their spinal cords by olfactory ensheathing glia.
Neuron, 25 (2000), pp. 425-435
[19.]
T. Takami, M. Oudega, M.L. Bates, P.M. Wood, N. Kleitman, M.B. Bunge.
Schwann cells but not olfactory ensheathing glia transplants improve hindlimb locomotor performance in the moderately contused adult rat thoracic spinal cord.
J Neurosci, 22 (2002), pp. 6670-6681
[20.]
G.W. Plant, C.L. Christensen, M. Oudega, M.B. Bunge.
Delayed transplantation of olfactory ensheathing glia promotes sparing/ regeneration of supraspinal axons in the contused adult rat spinal cord.
J Neurotrauma, 20 (2003), pp. 1-16
[21.]
E. Woodhall, A.K. West, M.I. Chuah.
Cultured olfactory ensheathing cells express nerve growth factor, brain-derived neurotrophic factor, glia cell line-derived neurotrophic factor and their receptors.
Mol Brain Res, 88 (2001), pp. 203-213
[22.]
Y. Liu, D. Kim, B.T. Himes, S.Y. Chow, T. Schallert, M. Murray, et al.
Transplants of fibroblasts genetically modified to express BDNF promote regeneration of adult rat rubrospinal axons and recovery of forelimb function.
J Neurosci, 19 (1999), pp. 4370-4387
[23.]
P. Lu, A. Blesch, M.H. Tuszynski.
Neurotrophism without neurotropism: BDNF promotes survival but not growth of lesioned corticospinal neurons.
J Comp Neurol, 436 (2001), pp. 456-470
[24.]
P.C. Holm, P. Akerud, J. Wagner, E. Arenas.
Neurturin is a neuritogenic but not a survival factor for developing and adult central noradrenergic neurons.
J Neurochem, 81 (2002), pp. 1318-1327
[25.]
A. Ramón-Cueto, J. Avila.
Olfactory ensheathing glia: properties and function.
Brain Res Bull, 46 (1998), pp. 175-187
[26.]
D.M. Snow, J.D. Smith, J.A. Gurwell.
Binding characteristics of chondroitin sulfate proteoglycans and laminin-1, and correlative neurite outgrowth behaviors in a standard tissue culture choice assay.
J Neurobiol, 51 (2002), pp. 285-301
[27.]
H.N. Nash, R.C. Borke, J.J. Anders.
Ensheathing cells and methylprednisolone promote axonal regeneration and functional recovery in the lesioned adult rat spinal cord.
J Neurosci, 22 (2002), pp. 7111-7120
[28.]
P.M. Richardson, U.M. McGuinness, A.J. Aguayo.
Axons from CNS neurons regenerate into PNS grafts.
Nature, 20 (1980), pp. 264-265
[29.]
J.D. Guest, A. Rao, L. Olson, M.B. Bunge, R.P. Bunge.
The ability of human Schwann cell grafts to promote regeneration in the transected nude rat spinal cord.
Exp Neurol, 148 (1997), pp. 502-522
[30.]
A. Ramón-Cueto, G.W. Plant, J. Avila, M.B. Bunge.
Long-distance axonal regeneration in the transected adult rat spinal cord is promoted by olfactory ensheathing glia transplants.
J Neurosci, 18 (1998), pp. 3803-3815
Copyright © 2005. Sociedad Española de Cirugia Ortopédica y Traumatología (SECOT)
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