Modulating astrogliosis after neurotrauma

Traumatic injury to the adult central nervous system (CNS) results in a rapid response from resident astrocytes, a process often referred to as reactive astrogliosis or glial scarring. The robust formation of the glial scar and its associated extracellular matrix (ECM) molecules have been suggested to interfere with any subsequent neural repair or CNS axonal regeneration. A series of recent in vivo experiments has demonstrated a distinct inhibitory influence of the glial scar on axonal regeneration. Here we review several experimental strategies designed to elucidate the roles of astrocytes and their associated ECM molecules after CNS damage, including astrocyte ablation techniques, transgenic approaches, and alterations in the deposition of the ECM. In the short term, mediators that modulate the inflammatory mechanisms responsible for eliciting astrogliotic scaring hold strong potential for establishing a favorable environment for neuronal repair. In the future, the conditional (inducible) genetic manipulation of astrocytes holds promise for further increasing our understanding of the functional biology of astrocytes as well as opening new therapeutic windows. Nevertheless, it is most likely that, to obtain long distance axonal regeneration within the injured adult CNS, a combinatorial approach involving different repair strategies, including but not limited to astrogliosis modulation, will be required. J. Neurosci. Res. 63:109–115, 2001. © 2001 Wiley‐Liss, Inc.

[1]  L. Eng Glial fibrillary acidic protein (GFAP): the major protein of glial intermediate filaments in differentiated astrocytes , 1985, Journal of Neuroimmunology.

[2]  T. Ferguson,et al.  Neuronal Matrix Metalloproteinase-2 Degrades and Inactivates a Neurite-Inhibiting Chondroitin Sulfate Proteoglycan , 1998, The Journal of Neuroscience.

[3]  T. Ferguson,et al.  Degradation of Chondroitin Sulfate Proteoglycan Enhances the Neurite-Promoting Potential of Spinal Cord Tissue , 1998, Experimental Neurology.

[4]  M. Sporn,et al.  Effects of transforming growth factor beta 1 on scar production in the injured central nervous system of the rat. , 1994, The European journal of neuroscience.

[5]  G. Giannelli,et al.  Induction of cell migration by matrix metalloprotease-2 cleavage of laminin-5. , 1997, Science.

[6]  J. Silver,et al.  Glial cell extracellular matrix: boundaries for axon growth in development and regeneration , 1997, Cell and Tissue Research.

[7]  M. Eddleston,et al.  Molecular profile of reactive astrocytes—Implications for their role in neurologic disease , 1993, Neuroscience.

[8]  Tomoko Kobayashi,et al.  Effect of transforming growth factor β 1 on spinal motor neurons after axotomy , 1997, Journal of the Neurological Sciences.

[9]  R. Saxod,et al.  Involvement of a chondroitin sulfate proteoglycan in the avoidance of chick epidermis by dorsal root ganglia fibers: a study using beta-D-xyloside. , 1991, Developmental biology.

[10]  M. Berry,et al.  Inhibition of glial scarring in the injured rat brain by a recombinant human monoclonal antibody to transforming growth factor‐β2 , 1999, The European journal of neuroscience.

[11]  T. Hattori,et al.  Fine structural changes in the rat brain after local injections of gliotoxin, alpha-aminoadipic acid. , 1986, Histology and histopathology.

[12]  J. Fawcett,et al.  Increased axon regeneration in astrocytes grown in the presence of proteoglycan synthesis inhibitors. , 1995, Journal of cell science.

[13]  M. Hatten,et al.  Astroglia in CNS injury , 1991, Glia.

[14]  K. Suzuki,et al.  Demyelination and remyelination in the rat central nervous system following ethidium bromide injection. , 1979, Laboratory investigation; a journal of technical methods and pathology.

[15]  N. Bulleid,et al.  Molecular recognition in procollagen chain assembly. , 1998, Matrix biology : journal of the International Society for Matrix Biology.

[16]  Clive N Svendsen,et al.  Leukocyte Infiltration, Neuronal Degeneration, and Neurite Outgrowth after Ablation of Scar-Forming, Reactive Astrocytes in Adult Transgenic Mice , 1999, Neuron.

[17]  U. Lendahl,et al.  Abnormal Reaction to Central Nervous System Injury in Mice Lacking Glial Fibrillary Acidic Protein and Vimentin , 1999, The Journal of cell biology.

[18]  M. Tuszynski,et al.  Elimination of Basal Lamina and the Collagen “Scar” after Spinal Cord Injury Fails to Augment Corticospinal Tract Regeneration , 1999, Experimental Neurology.

[19]  M. Schwab,et al.  Secondary Cell Death and the Inflammatory Reaction After Dorsal Hemisection of the Rat Spinal Cord , 1994, The European journal of neuroscience.

[20]  H. Luhmann,et al.  Inhibition of collagen IV deposition promotes regeneration of injured CNS axons , 1999, The European journal of neuroscience.

[21]  R. van der Neut Targeted gene disruption: applications in neurobiology. , 1997, Journal of neuroscience methods.

[22]  J. Steeves,et al.  Engines, Accelerators, and Brakes on Functional Spinal Cord Repair a , 1998, Annals of the New York Academy of Sciences.

[23]  A. Faissner The tenascin gene family in axon growth and guidance , 1997, Cell and Tissue Research.

[24]  R. Iozzo Matrix proteoglycans: from molecular design to cellular function. , 1998, Annual review of biochemistry.

[25]  C. Kozak,et al.  Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene , 1994, Nature Genetics.

[26]  C. Betsholtz,et al.  Mice lacking glial fibrillary acidic protein display astrocytes devoid of intermediate filaments but develop and reproduce normally. , 1995, The EMBO journal.

[27]  Douglas K. Anderson,et al.  Chondroitin Sulfate Proteoglycan Immunoreactivity Increases Following Spinal Cord Injury and Transplantation , 1999, Experimental Neurology.

[28]  J. Silver,et al.  Inflammation and the glial scar: Factors at the site of injury that influence regeneration in the central nervous system , 2000 .

[29]  R. Markwald,et al.  The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation. , 1998, Developmental biology.

[30]  D. Steindler,et al.  Tenascin knockout mice: barrels, boundary molecules, and glial scars , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  J. Fawcett,et al.  The glial scar and central nervous system repair , 1999, Brain Research Bulletin.

[32]  S. K. Malhotra,et al.  Reactive astrocytes: cellular and molecular cues to biological function , 1997, Trends in Neurosciences.

[33]  Jonas Frisén,et al.  Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System , 1999, Cell.

[34]  A. Messing,et al.  Axonal and Nonneuronal Cell Responses to Spinal Cord Injury in Mice Lacking Glial Fibrillary Acidic Protein , 1997, Experimental Neurology.

[35]  Pauline M. Field,et al.  Regeneration of Cut Adult Axons Fails Even in the Presence of Continuous Aligned Glial Pathways , 1996, Experimental Neurology.

[36]  G. Ivy,et al.  Selective ablation of astrocytes by intracerebral injections of alpha-aminoadipate. , 1996, Glia.

[37]  J. Silver,et al.  Robust Regeneration of Adult Sensory Axons in Degenerating White Matter of the Adult Rat Spinal Cord , 1999, The Journal of Neuroscience.

[38]  J. Mallet,et al.  Effects of Spinal Cord X-irradiation on the Recovery of Paraplegic Rats , 2000, Experimental Neurology.

[39]  M. Risling,et al.  Rapid, widespread, and longlasting induction of nestin contributes to the generation of glial scar tissue after CNS injury , 1995, The Journal of cell biology.

[40]  Z. Fuks,et al.  Structural recovery in lesioned adult mammalian spinal cord by x-irradiation of the lesion site. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[41]  C. Lobe,et al.  Conditional genome alteration in mice , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

[42]  J. Boya,et al.  Ultrastructural study on meningeal regeneration and meningo-glial relationships after cerebral stab wound in the adult rat , 1988, Brain Research.

[43]  D. Friedlander,et al.  Functions of brain chondroitin sulfate proteoglycans during developments: interactions with adhesion molecules. , 1996, Perspectives on developmental neurobiology.

[44]  R. Iozzo,et al.  Transcriptional and posttranscriptional regulation of proteoglycan gene expression. , 1999, Progress in nucleic acid research and molecular biology.

[45]  Y Ikawa,et al.  Mice develop normally without tenascin. , 1992, Genes & development.

[46]  B. Stokes,et al.  Localization of Transforming Growth Factor-β1 and Receptor mRNA after Experimental Spinal Cord Injury , 2000, Experimental Neurology.

[47]  V. Yong,et al.  Attenuation of Astroglial Reactivity by Interleukin-10 , 1996, The Journal of Neuroscience.

[48]  E. Albuquerque,et al.  Ineffectiveness of enzyme therapy on regeneration in the transected spinal cord of the rat. , 1980, Journal of neurosurgery.

[49]  J. Silver,et al.  Injury-Induced Proteoglycans Inhibit the Potential for Laminin-Mediated Axon Growth on Astrocytic Scars , 1995, Experimental Neurology.

[50]  H. Yip,et al.  Chondroitinase ABC promotes axonal regeneration of Clarke's neurons after spinal cord injury , 2000, Neuroreport.

[51]  S. B. Kater,et al.  Myelin‐associated glycoprotein inhibits neurite/axon growth and causes growth cone collapse , 1996, Journal of neuroscience research.

[52]  R. Yezierski,et al.  Neuroprotective Effects of Interleukin-10 Following Excitotoxic Spinal Cord Injury , 1999, Experimental Neurology.

[53]  D. Muir Metalloproteinase-dependent neurite outgrowth within a synthetic extracellular matrix is induced by nerve growth factor. , 1994, Experimental cell research.

[54]  Voon Wee Yong,et al.  Matrix metalloproteinases and diseases of the CNS , 1998, Trends in Neurosciences.

[55]  F. Matsui,et al.  Molecular interactions of neural chondroitin sulfate proteoglycans in the brain development. , 2000, Archives of biochemistry and biophysics.

[56]  Z. Fuks,et al.  Severed corticospinal axons recover electrophysiologic control of muscle activity after x-ray therapy in lesioned adult spinal cord. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[57]  M. Norenberg,et al.  Astrocyte Responses to CNS Injury , 1994, Journal of neuropathology and experimental neurology.

[58]  M. Gossen,et al.  Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[59]  M. Nieto‐Sampedro,et al.  Neurite Outgrowth Inhibitor of Gliotic Brain Tissue. Mode of Action and Cellular Localization, Studied with Specific Monoclonal Antibodies , 1997, The European journal of neuroscience.

[60]  G. Ivy,et al.  Selective ablation of astrocytes by intracerebral injections of α‐aminoadipate , 1996 .

[61]  J. Fawcett,et al.  Robust Regeneration of CNS Axons through a Track Depleted of CNS Glia , 2000, Experimental Neurology.

[62]  J. Martinou,et al.  Transforming growth factor beta 1 is a potent survival factor for rat embryo motoneurons in culture. , 1990, Brain research. Developmental brain research.

[63]  A. Messing,et al.  Conditional Ablation of Cerebellar Astrocytes in Postnatal Transgenic Mice , 1996, The Journal of Neuroscience.