Chapter 31: CNS glial scar tissue: a source of molecules which inhibit central neurite outgrowth

Publisher Summary The chapter describes the interactions between purified gliotic membranes and embryonic central nervous system (CNS) explants. Gliotic membranes have different effects on neurite outgrowth, depending on whether the lesion is isomorphic or anisomorphic. The partial characterization of a proteoglycan associated with isomorphic gliotic membranes, which appears to inhibit central neurite outgrowth is also described. The major component of the glial scar is reactive glia. Reactive glia formation is the most general and stereotyped reaction of the CNS to any type of insult. From a neuropathological point of view, gliosis can be classified as anisomorphic or isomorphic, based on whether the eliciting stimulus is an open injury. Plasma membranes isolated from fresh tissue maintain the characteristics of the living cell surface; therefore, plasma membranes are isolated from glial scar tissue to study directly the interaction of growing axons with the scar cellular components, predominantly reactive astrocytes and microglial cells.

[1]  Erkki Ruoslahti,et al.  Proteoglycans as modulators of growth factor activities , 1991, Cell.

[2]  D. Steindler,et al.  Molecular and cellular characterization of the glial roof plate of the spinal cord and optic tectum: a possible role for a proteoglycan in the development of an axon barrier. , 1990, Developmental biology.

[3]  T. Carlstedt,et al.  Regrowth of lesioned dorsal root nerve fibers into the spinal cord of neonatal rats , 1987, Neuroscience Letters.

[4]  M. Schwab,et al.  Oligodendrocytes and CNS myelin are nonpermissive substrates for neurite growth and fibroblast spreading in vitro , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  G. Raisman,et al.  Astrocyte cultures from adult rat brain. Derivation, characterization and neurotrophic properties of pure astroglial cells from corpus callosum , 1982, Brain Research.

[6]  A. Bignami,et al.  Vimentin in the central nervous system. A study of the mesenchymal-type intermediate filament-protein in Wallerian degeneration and in postnatal rat development by two-dimensional gel electrophoresis. , 1982, Differentiation; research in biological diversity.

[7]  M. Nieto‐Sampedro Growth Factor Induction and Order of Events in CNS Repair , 1988 .

[8]  R. Lasek,et al.  Astrocytes block axonal regeneration in mammals by activating the physiological stop pathway. , 1987, Science.

[9]  Jonathan A. Raper,et al.  The enrichment of a neuronal growth cone collapsing activity from embryonic chick brain , 1990, Neuron.

[10]  S. Hall,et al.  The response of regenerating peripheral neuntes to a grafted optic nerve , 1987, Journal of neurocytology.

[11]  M. Nieto‐Sampedro Astrocyte mitogen inhibitor related to epidermal growth factor receptor. , 1988, Science.

[12]  K. Kalil,et al.  A light and electron microscopic study of regrowing pyramidal tract fibers , 1982, The Journal of comparative neurology.

[13]  M. Schwab,et al.  Channeling of developing rat corticospinal tract axons by myelin- associated neurite growth inhibitors , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  A. Lander,et al.  A diverse set of developmentally regulated proteoglycans is expressed in the rat central nervous system , 1990, Neuron.

[15]  J. Kruse,et al.  J1/tenascin is a repulsive substrate for central nervous system neurons , 1990, Neuron.

[16]  J. Kapfhammer,et al.  Interactions between growth cones and neurites growing from different neural tissues in culture , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  E. Engvall,et al.  Schwannoma cell-derived inhibitor of the neurite-promoting activity of laminin , 1989, The Journal of cell biology.

[18]  Robert B. Nelson,et al.  Expression of β-amyloid precursor protein in reactive astrocytes following neuronal damage , 1989, Neuron.

[19]  P. Bovolenta,et al.  Neurite outgrowth over resting and reactive astrocytes. , 1991, Restorative neurology and neuroscience.

[20]  M. Raff Glial cell diversification in the rat optic nerve. , 1989, Science.

[21]  K. Janeczko Spatiotemporal patterns of the astroglial proliferation in rat brain injured at the postmitotic stage of postnatal development: a combined immunocytochemical and autoradiographic study , 1989, Brain Research.

[22]  R. Lund,et al.  Development of fetal retina, tectum, and cortex transplanted to the superior colliculus of adult rats , 1983, The Journal of comparative neurology.

[23]  M. Schwab,et al.  Two membrane protein fractions from rat central myelin with inhibitory properties for neurite growth and fibroblast spreading , 1988, The Journal of cell biology.

[24]  M. Graeber,et al.  Functional plasticity of microglia: A review , 1988, Glia.

[25]  J. Fawcett,et al.  Oligodendrocytes repel axons and cause axonal growth cone collapse. , 1989, Journal of cell science.

[26]  M. Schwab,et al.  Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associated neurite growth inhibitors , 1990, Nature.

[27]  Cavanagh Jb,et al.  The proliferation of astrocytes around a needle wound in the rat brain. , 1970 .

[28]  J. Silver,et al.  Sulfated proteoglycans in astroglial barriers inhibit neurite outgrowth in vitro , 1990, Experimental Neurology.

[29]  P. Caroni,et al.  Antibody against myelin associated inhibitor of neurite growth neutralizes nonpermissive substrate properties of CNS white matter , 1988, Neuron.

[30]  N. Heisterkamp,et al.  C‐abl and bcr are rearranged in a Ph1‐negative CML patient. , 1985, The EMBO journal.

[31]  J. Sanes,et al.  Extracellular matrix molecules that influence neural development. , 1989, Annual review of neuroscience.

[32]  F. Gomez-Pinilla,et al.  Epidermal growth factor receptor immunoreactivity in rat brain astrocytes. Response to injury , 1988, Neuroscience Letters.

[33]  Edward C. Cox,et al.  Axonal guidance in the chick visual system: Posterior tectal membanes induce collapse of growth cones from the temporal retina , 1990, Neuron.

[34]  J. Silver,et al.  Inhibition of neurite outgrowth on astroglial scars in vitro , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  H. Ralston,et al.  The cellular reaction to Wallerian degeneration in the central nervous system of the cat. , 1969, Brain research.

[36]  R. Keynes,et al.  Isolation from chick somites of a glycoprotein fraction that causes collapse of dorsal root ganglion growth cones , 1990, Neuron.

[37]  M. Schwab,et al.  Responses of Regenerating Rat Retinal Ganglion Cell Axons to Contacts with Central Nervous Myelin in vitro , 1990, The European journal of neuroscience.

[38]  L. Landmesser,et al.  Development of the major pathways for neurite outgrowth in the chick hindlimb. , 1985, Developmental biology.

[39]  A. Lander Understanding the molecules of neural cell contacts: emerging patterns of structure and function , 1989, Trends in Neurosciences.

[40]  M. Graeber,et al.  New expression of myelomonocytic antigens by microglia and perivascular cells following lethal motor neuron injury , 1990, Journal of Neuroimmunology.

[41]  C. Bandtlow,et al.  Oligodendrocytes arrest neurite growth by contact inhibition , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  J. A. Cifonelli,et al.  [7] Isolation and characterization of connective tissue polysaccharides , 1972 .

[43]  A. Scheibel,et al.  Degeneration and regeneration of the nervous system , 1960 .

[44]  S. Kater,et al.  Regulation of growth cone behavior by calcium , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  S. Carbonetto,et al.  Nerve fiber growth in culture on fibronectin, collagen, and glycosaminoglycan substrates , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  J W Fawcett,et al.  The growth of axons in three-dimensional astrocyte cultures. , 1989, Developmental biology.

[47]  P. Patterson On the importance of being inhibited, or saying no to growth cones , 1988, Neuron.

[48]  M. Schachner,et al.  J1-160 and J1-180 are oligodendrocyte-secreted nonpermissive substrates for cell adhesion , 1989, The Journal of cell biology.

[49]  R. Pearce,et al.  Fractionation of anionic glycosaminoglycans by ion-exchange chromatography. , 1968, Analytical biochemistry.

[50]  E. Geisert,et al.  Expression of microtubule-associated protein 2 by reactive astrocytes. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[51]  P. Liesi Laminin‐immunoreactive glia distinguish regenerative adult CNS systems from non‐regenerative ones. , 1985, The EMBO journal.

[52]  A. Aguayo,et al.  Axonal elongation into peripheral nervous system "bridges" after central nervous system injury in adult rats. , 1981, Science.

[53]  R. U. Margolis,et al.  Structure and Localization of Glycoproteins and Proteoglycans , 1989 .

[54]  A. Bignami,et al.  THE ASTROGLIAL RESPONSE TO STABBING. IMMUNOFLUORESCENCE STUDIES WITH ANTIBODIES TO ASTROCYTE‐SPECIFIC PROTEIN (GFA) IN MAMMALIAN AND SUBMAMMALIAN VERTEBRATES , 1976 .

[55]  A. Aguayo,et al.  Axons from CNS neurones regenerate into PNS grafts , 1980, Nature.