Effects of Schwann Cell Transplantation in a Contusion Model of Rat Spinal Cord InjuryMartin, Didier ; Robe, Pierre ; Franzen, Rachelle et alin Journal of Neuroscience Research (1996), 45(5), 588-597 Cultured Schwann cells were transplanted at various delays into a spinal cord contusion injury performed at low thoracic level in adult female rats. The Schwann cells were purified from the dorsal root ... [more ▼] Cultured Schwann cells were transplanted at various delays into a spinal cord contusion injury performed at low thoracic level in adult female rats. The Schwann cells were purified from the dorsal root ganglia of adult syngeneic animals. the transplants were well tolerated, and the transplanted Schwann cells invaded the injured spinal cord. As quantified using video image analysis, the survival and growth of the transplanted cells were poor when the grafting procedure was performed 3-4 days after injury and very good when performed immediately or 10 days after injury, in which cases post-traumatic micro- and macrocavitation were strongly reduced. In animals grafted immediately after injury but not in animals grafted after 10 days, post-traumatic astrogliosis was much reduced. The Schwann cells transplanted area was invaded by numerous regenerating axons, the vast majority of which were, based on the neurotransmitter (CGRP and SP) profile, originating from dorsal root ganglion. No regeneration of the corticospinal tract as assessed after anterograde tracing or of descending aminergic fibers could be demonstrated. [less ▲] Detailed reference viewed: 30 (5 ULg) Neurotrophic Factors: Past and FutureMoonen, Gustave ; Malgrange, Brigitte ; et alin Acta Neurologica Belgica (1996), 96(3), 203-18 Detailed reference viewed: 9 (1 ULg) Porous biomaterials tailored for cell culture.Grandfils, Christian ; ; et alin Cytotechnology (1996), 21 Detailed reference viewed: 8 (0 ULg) In vitro expression of RC2-labeled antigens as radial glial cells markers in cultures derived from mouse embryonic brain; ; et al Poster (1996) Detailed reference viewed: 2 (0 ULg) Identification of antigens recognized in the developing mouse brain by the RC2 antibody, a marker of radial gliaLeprince, Pierre ; ; et alin International Journal of Developmental Neuroscience (1996), 14(Sup. 1), 84 Detailed reference viewed: 13 (6 ULg) Surface modification of biomaterials in order to control cell adhesion.; ; et al Conference (1996) Detailed reference viewed: 6 (3 ULg) Alpha-MSH stimulates neurite outgrowth of neonatal rat corticospinal neurons in vitro.; ; Martin, Didier et alin Brain Research (1996), 736(1-2), 91-8 Peptides related to melanocortin (alpha MSH) and corticotropin (ACTH), collectively termed melanocortins, exert trophic effects on the outgrowth of neurites from peripheral and central nervous system in ... [more ▼] Peptides related to melanocortin (alpha MSH) and corticotropin (ACTH), collectively termed melanocortins, exert trophic effects on the outgrowth of neurites from peripheral and central nervous system in vitro. Here we study the neurite outgrowth promoting effect of alpha-MSH on corticospinal (CS) neurons in vitro. Corticospinal neurons were identified in cell culture of neonatal rat cortex by immunostaining of cholera toxin subunit B (CTB), retrogradely transported from the cervical parts of the spinal cord. The CTB-immunoreactive neurons represent a small percentage (3-5%) of the total cell population after 72 h in vitro. The axons or dendrites of cortical and CTB-labelled layer V neurons were visualized using antibodies against axon- or dendrite-specific markers and measured using a semi-automatic quantification device. Here we report that alpha-MSH stimulates axonal as well as dendrite outgrowth from both total and CTB-labelled neurons with a bell-shape response curve. Axonal outgrowth of CTB-labelled neurons was dose-dependently stimulated with a maximal effect of 50% at 10(-10) M alpha-MSH. The maximal effect for stimulation of axon outgrowth for the total cortex population was observed at 10(-8) M alpha-MSH. In addition dendrite outgrowth of both total and CTB-labelled neurons is stimulated in a dose-dependent manner with maximal effects (varying between 46 and 48%) at 10(-8) M alpha-MSH. Explanations in the shift for the optimal alpha-MSH concentration for stimulation of axonal outgrowth of CTB-labelled layer V neurons as compared to total cortex neurons are discussed. [less ▲] Detailed reference viewed: 24 (0 ULg) Astroglia-released factor with negative allosteric modulatory properties at the GABA A receptor.; Belachew, Shibeshih ; et alin Biochemical Pharmacology (1996), 52(3), 465-473 We have previously shown, using whole-cell patch-clamp techniques, that astrocytes release a negative allosteric modulator of the gamma-aminobutyric acid type A receptor (GABAA receptor) with beta ... [more ▼] We have previously shown, using whole-cell patch-clamp techniques, that astrocytes release a negative allosteric modulator of the gamma-aminobutyric acid type A receptor (GABAA receptor) with beta-carboline-like properties, thus, likely to act at the benzodiazepine site. Here, using patch-clamp and binding techniques, we confirm that the low-molecular-weight fraction of astroglia-conditioned medium (ACM lmf) contains a factor(s) that negatively modulates GABAA-receptor function. This factor, like beta-carbolines, enhances the specific binding of [35S]t-butyl bicyclophosphorothionate (TBPS) to adult rat cortical membranes in the presence of GABA. However, it fails to interact with various ligands of the benzodiazepine (BZD) site of the GABAA receptor ([3H]flunitrazepam, [3H]Ro 15-1788 and [3H]Ro 15-4513). The question of the actual binding site of the astroglia-derived factor on the GABAA receptor, thus, remains open and can be addressed only after the purification of the active molecule(s) of ACM Imf has been completed, and a labeled form of the endogenous ligand becomes available. Taken together, however, the data suggest that type 1 astrocytes are able to modulate the effects of the main inhibitory neurotransmission in the central nervous system. [less ▲] Detailed reference viewed: 18 (1 ULg) Fluorescence detection of a neurotoxic astroglia-released factor after precol-umn derivatization and gradient liquid chromatographyHubert, Philippe ; Hurlet, Vincent ; et alPoster (1996) Detailed reference viewed: 4 (2 ULg) Preparation of a Macroporous Biodegradable Polylactide Implant for Neuronal Transplantation; Grandfils, Christian ; Jérôme, Robert et alin Journal of Biomedical Materials Research (1995), 29(11), 1349-62 This article reports the production of a surgical implant meeting several specific requirements such as biocompatibility, biodegradability, macroporosity, and flexibility. Porosity was controlled by an ... [more ▼] This article reports the production of a surgical implant meeting several specific requirements such as biocompatibility, biodegradability, macroporosity, and flexibility. Porosity was controlled by an original method consisting of the aggregation of calibrated poly-D,L-lactide microparticles. The size of the interstices between the aggregated microspheres was in a direct relationship to the microsphere diameter. A first approach was based on coating the microspheres with poly(vinyl alcohol) followed by chemically crosslinking the coating layers that were in mutual contact. This method was disregarded because of the acute cytotoxicity of glutaraldehyde used as the crosslinking agent, the absence of macroporosity, and the complete lack of flexibility. A physical technique of aggregation was then tested, which relied on the plasticization of poly-D,L-lactide microspheres with triethylcitrate to the point where microspheres strongly adhered to each other when they were in contact. This method has proved to be straightforward and definitely superior to the chemical approach, particularly with respect to cytotoxicity, control of macroporosity, and flexibility. A polymer support was thus successfully which was biodegradable, macroporous( interconnected pores of 10-100 microns in diameter), and flexible. This potential medical device is presently being used for neuronal transplantation in the central nervous system. [less ▲] Detailed reference viewed: 22 (5 ULg) Quantitative assessment by western-blot of proteins expressed by different cell types involved in inhibition and promotion of regeneration in the lesioned spinal cord.; Martin, Didier ; Leprince, Pierre et alConference (1995, September 21) Detailed reference viewed: 1 (0 ULg) A model of spinal cord injury: the balloon-compressive modelMartin, Didier ; ; Robe, Pierre et alConference (1995, September 03) Detailed reference viewed: 2 (0 ULg) Porous biomaterials tailored for cell cultureGrandfils, Christian ; ; et alConference (1995, May 29) Effects of macrophage grafts on the expression of glial and neuronal markers in the lesioned adult rat spinal cord: a combined immunocytochemical and biochemical study.; Martin, Didier ; Leprince, Pierre et alConference (1995, May 09) Detailed reference viewed: 3 (0 ULg) Les transplantations de cellules de Schwann syngéniques dans les lésions médullaires : résultats, limitations et perspectivesMartin, Didier ; Schoenen, Jean ; Robe, Pierre et alConference (1994, November 06) Detailed reference viewed: 5 (1 ULg) Astroglia-Released Factor Shows Similar Effects as Benzodiazepine Inverse Agonists; Belachew, Shibeshih ; et alin Journal of Neuroscience Research (1994), 39(4), 364-76 Media conditioned by cultured neonatal cerebral cortex microexplants (CCM) or astrocytes (ACM) contain low molecular weight (< 1,000 Da) substance(s) which inhibits the gamma aminobutyric acid (GABA ... [more ▼] Media conditioned by cultured neonatal cerebral cortex microexplants (CCM) or astrocytes (ACM) contain low molecular weight (< 1,000 Da) substance(s) which inhibits the gamma aminobutyric acid (GABA)-induced inward current recorded in cerebellar granule cells and hippocampal neurons in culture using the whole-cell patch-clamp technique. This effect is specific for CCM and ACM, as medium conditioned by PC12 cells (PC12CM) does not affect the GABA response of these cells. It is also specific for GABA-induced currents because glutamate-induced currents do not change either in amplitude or in shape in the presence of CCM or ACM. The inhibitory effect on the GABA response in cerebellar granule cells of both ACM and CCM could be suppressed by flumazenil, a specific benzodiazepine (BZD) antagonist and could be mimicked by two BZD inverse agonists. These data thus demonstrate the presence of a BZD inverse agonist-like activity in CCM and ACM. This effect of ACM on different neuronal cell types was heterogenous since no detectable effect could be observed on the GABA-induced current in GABA-responsive dorsal root ganglion (DRG) neurons, presumably reflecting a functional heterogeneity of the GABAA receptors present in these different neuronal subsets. By the release of such an endogenous BZD inverse agonist-like activity, glia cells could possibly modulate GABAA receptor-mediated responses. [less ▲] Detailed reference viewed: 17 (5 ULg) Propofol Protects Cultured Rat Hippocampal Neurons against N-Methyl-D-Aspartate Receptor-Mediated Glutamate ToxicityHans, Pol ; Bonhomme, Vincent ; Collette, Julien et alin Journal of Neurosurgical Anesthesiology (1994), 6(4), 249-53 The effect of propofol on the toxicity induced by glutamate (GLU), N-methyl-D-aspartate (NMDA), kainate (KA), and amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) was investigated on cultured ... [more ▼] The effect of propofol on the toxicity induced by glutamate (GLU), N-methyl-D-aspartate (NMDA), kainate (KA), and amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) was investigated on cultured fetal rat hippocampal neurons. The degree of neuronal injury was quantified by measuring the release of the neuron-specific enolase (NSE) into the culture media. The toxicity induced by brief exposure to GLU (10(-4) M) or to NMDA (10(-4) M) was significantly reduced by propofol, whereas that elicited by KA, AMPA (10(-4) M), or long GLU exposure was unaffected. In conclusion, high concentrations of propofol significantly attenuate NMDA receptor-mediated glutamate neurotoxicity in vitro. Further studies are needed to confirm this beneficial effect in vivo and to evaluate propofol as a neuroprotective anesthetic agent in pathologies involving glutamate release and NMDA-mediated toxicity. [less ▲] Detailed reference viewed: 6 (0 ULg) Radiation-Induced Myelopathy and Vertebral NecrosisMartin, Didier ; Delacollette, Mireille ; Collignon, Jacques et alin Neuroradiology (1994), 36(5), 405-7 Radiation-induced myelopathy is often a diagnosis of exclusion. In addition to the classic criteria needed to support the diagnosis, the presence of another radiation-induced lesion, such as aseptic ... [more ▼] Radiation-induced myelopathy is often a diagnosis of exclusion. In addition to the classic criteria needed to support the diagnosis, the presence of another radiation-induced lesion, such as aseptic vertebral necrosis, is useful to confirm the cause of the spinal cord lesion. [less ▲] Detailed reference viewed: 39 (7 ULg) Tailoring of a macroporous biodegradable polylactide surgical implant for neuronal transplantation and axonal regeneration and axonal regeneration; ; Grandfils, Christian et alPoster (1994, April 12) Detailed reference viewed: 1 (0 ULg) Hypothèses étiopathologiques récentes dans la maladie d'Alzheimer: apports de la biologie moléculaireMoonen, Gustave ; Rogister, Bernard ; Leprince, Pierre ![]() in Revue Médicale de Liège (1994), 49(2), 78-83 Detailed reference viewed: 5 (1 ULg) |
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