Hydrogels Containing Peptide or Aminosugar Sequences Implanted into the Rat Brain: Influence on Cellular Migration and Axonal Growth

Biocompatible polymer matrices for implantation into lesion sites in the brain were synthesized by incorporating peptide or aminosugar sequences into N-(2-hydroxypropyl)methacrylamide (HPMA) hydrogels. RGD peptide sequences were chemically linked to the hydrogel backbone via a glycylglycine spacer; aminosugars were glucosamine (NHGlc) or N-acetylglucosamine residues. Unmodified or sequence containing HPMA hydrogels were implanted into the lesioned optic tract or cerebral cortex of juvenile (17- to 19-day-old) or adult rat brains, respectively. After 10-12 months host animals were perfused and the brains were processed for immunohistochemistry using antibodies to neurofilaments (RT97), laminin, glial fibrillary acidic protein (GFAP), carbonic anhydrase II (CAII), S100 protein, macrophages (ED1), and myelin basic protein (MBP). Unmodified (control) HPMA hydrogels contained no cellular infiltration or axonal growth. Peptide (RGD)- and aminosugar-modified hydrogels showed increased adhesion properties with host neural tissue, were vascularized, and were infiltrated by host nonneuronal cells. Astrocytes (GFAP+) and macrophages (ED1(+)) were the major cell types seen within modified HPMA hydrogels, the largest numbers being found in RGD-containing polymers. CAII+ oligodendroglia were not seen within any of the hydrogel matrices. RT97(+)/MBP- axons grew into both the RGD and NHGlc hydrogel matrices for small distances. The number of axons was greatest in hydrogels implanted into cerebral cortex but in both cortex and optic tract implants the highest density of axons was seen in polymers containing RGD. The findings of this study are discussed in the context of CNS tissue replacement and the construction of bioactive scaffolds to promote regenerative axonal growth across areas of injury in the brain and spinal cord.

[1]  N. Tawil,et al.  Expression and distribution of functional intergrins in rat CNS glia , 1994, Journal of neuroscience research.

[2]  J. C. Torre,et al.  Catecholamine fiber regeneration across a collagen bioimplant after spinal cord transection , 1982, Brain Research Bulletin.

[3]  F. Roberge,et al.  Chemotaxis of rat retinal glia to growth factors found in repairing wounds. , 1987, Investigative ophthalmology & visual science.

[4]  A. Eklund,et al.  Regulated expression of integrins and other adhesion molecules during differentiation of monocytes into macrophages. , 1994, Cellular immunology.

[5]  T. Jessell,et al.  Cell surface glycoconjugates and carbohydrate-binding proteins: possible recognition signals in sensory neurone development. , 1986, The Journal of experimental biology.

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

[7]  L. Shaw,et al.  Macrophage interactions with laminin: PMA selectively induces the adherence and spreading of mouse macrophages on a laminin substratum , 1988, The Journal of cell biology.

[8]  Y. Ito,et al.  Materials for enhancing cell adhesion by immobilization of cell-adhesive peptide. , 1991, Journal of biomedical materials research.

[9]  H. Kleinman,et al.  Connective tissue proteins and phagocytic cell function. Laminin enhances complement and Fc-mediated phagocytosis by cultured human macrophages , 1985, The Journal of experimental medicine.

[10]  D. Steindler,et al.  Enhanced expression of the developmentally regulated extracellular matrix molecule tenascin following adult brain injury. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[11]  J. Šulc,et al.  The influence of hydrogel functional groups on cell behavior. , 1990, Journal of biomedical materials research.

[12]  E. Engvall,et al.  Mapping of domains in human laminin using monoclonal antibodies: localization of the neurite-promoting site , 1986, The Journal of cell biology.

[13]  A. Harvey,et al.  Regrowth of axons within Schwann cell-filled polycarbonate tubes implanted into the damaged optic tract and cerebral cortex of rats. , 1994, Restorative neurology and neuroscience.

[14]  Fred H. Gage,et al.  Reactive astrocytes are substrates for the growth of adult CNS axons in the presence of elevated levels of nerve growth factor , 1991, Neuron.

[15]  H. Driguez,et al.  Biomedical polymers bearing pendant 2‐N‐acetylglucosaminyl residues. Synthesis and polymerization of 2‐methacryloyloxyethyl and 1‐methyl‐2‐methacryloylamidoethyl glycosides , 1992 .

[16]  K. Ulbrich,et al.  Synthetic polymer derivatives as substrata for neuronal adhesion and growth , 1993, Brain Research Bulletin.

[17]  P C Letourneau,et al.  Neurite extension by peripheral and central nervous system neurons in response to substratum-bound fibronectin and laminin. , 1983, Developmental biology.

[18]  N. Tawil,et al.  Integrins in point contacts mediate cell spreading: factors that regulate integrin accumulation in point contacts vs. focal contacts , 1993, The Journal of cell biology.

[19]  N. Ip,et al.  Expression of Ciliary Neurotrophic Factor and the Neurotrophins – Nerve Growth Factor, Brain‐Derived Neurotrophic Factor and Neurotrophin 3—in Cultured Rat Hippocampal Astrocytes , 1992, The European journal of neuroscience.

[20]  A. Harvey,et al.  Regrowth of lesioned retinal axons associated with the transplantation of Schwann cells to the brachial region of the rat optic tract. , 1991, Restorative neurology and neuroscience.

[21]  S. Carbonetto The extracellular matrix of the nervous system , 1984, Trends in Neurosciences.

[22]  J. Bixby,et al.  N-cadherin and integrins: Two receptor systems that mediate neuronal process outgrowth on astrocyte surfaces , 1988, Neuron.

[23]  Kenneth M. Yamada,et al.  Adhesive recognition sequences. , 1991, The Journal of biological chemistry.

[24]  J. Silver,et al.  Reduction of neurite outgrowth in a model of glial scarring following CNS injury is correlated with the expression of inhibitory molecules on reactive astrocytes , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  E Ruoslahti,et al.  New perspectives in cell adhesion: RGD and integrins. , 1987, Science.

[26]  S. David,et al.  Macrophages can modify the nonpermissive nature of the adult mammalian central nervous system , 1990, Neuron.

[27]  B. Seckel,et al.  Neural Regeneration and Transplantation: Frontiers of Clinical Neuroscience , 1990 .

[28]  C. Mason,et al.  Astroglial differentiation is required for support of neurite outgrowth , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  B. Shur,et al.  Cell surface galactosyltransferase mediates the initiation of neurite outgrowth from PC12 cells on laminin , 1990, The Journal of cell biology.

[30]  K. Ulbrich,et al.  Intracerebral Implantation of Hydrogel-Coupled Adhesion Peptides: Tissue Reaction , 1995, Journal of neural transplantation & plasticity.

[31]  D. Marshak S100 beta as a neurotrophic factor. , 1990, Progress in brain research.

[32]  P Aebischer,et al.  Laminin oligopeptide derivatized agarose gels allow three‐dimensional neurite extension in vitro , 1995, Journal of neuroscience research.

[33]  R. Martini Expression and functional roles of neural cell surface molecules and extracellular matrix components during development and regeneration of peripheral nerves , 1994, Journal of neurocytology.

[34]  D. Lauffenburger,et al.  Integrin-cytoskeletal interactions in neuronal growth cones , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

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

[36]  M. Pierre,et al.  Effects of transforming growth factor‐β1 on the extracellular matrix and cytoskeleton of cultured astrocytes , 1993 .

[37]  U. Otten,et al.  Interleukin-1 β and tumor necrosis factor-α synergistically stimulate nerve growth factor (NGF) release from cultured rat astrocytes , 1990, Neuroscience Letters.

[38]  A. Harvey,et al.  Axonal growth within poly (2-hydroxyethyl methacrylate) sponges infiltrated with Schwann cells and implanted into the lesioned rat optic tract , 1995, Brain Research.

[39]  J. Bixby Diversity of axonal growth-promoting receptors and regulation of their function , 1992, Current Opinion in Neurobiology.

[40]  E. Jones,et al.  Growth of corticospinal axons on prosthetic substrates introduced into the spinal cord of neonatal rats. , 1987, Brain research.

[41]  M. Murata,et al.  Restoration of function by replacement of spinal cord segments in the rat , 1994, Nature.

[42]  S. David,et al.  Dibutyryl cAMP, interleukin‐1β, and macrophage conditioned medium enhance the ability of astrocytes to promote neurite growth , 1994 .

[43]  H. Müller,et al.  Relationship between injury-induced astrogliosis, laminin expression and axonal sprouting in the adult rat brain , 1994, Journal of neurocytology.

[44]  S. David,et al.  Laminin and heparan sulphate proteoglycan in the lesioned adult mammalian central nervous system and their possible relationship to axonal sprouting , 1988, Journal of neurocytology.

[45]  D. Snow,et al.  Interactions of developing neurons with the extracellular matrix , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  A. Björklund,et al.  Regeneration of the septohippocampal pathways in adult rats is promoted by utilizing embryonic hippocampal implants as bridges , 1981, Brain Research.

[47]  M. Pierschbacher,et al.  Concept and progress in the development of RGD‐containing peptide pharmaceuticals , 1995, Biopolymers.

[48]  B. Shur,et al.  Laminin fragment E8 mediates PC12 cell neurite outgrowth by binding to cell surface beta 1,4 galactosyltransferase , 1991, The Journal of cell biology.

[49]  M. Hynes,et al.  Selective expression of an endogenous lactose-binding lectin gene in subsets of central and peripheral neurons , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  S. Cullheim,et al.  Spinal axons in central nervous system scar tissue are closely related to laminin-immunoreactive astrocytes , 1995, Neuroscience.

[51]  M. Humphries,et al.  The molecular basis and specificity of integrin-ligand interactions. , 1990, Journal of cell science.

[52]  A. Kornblihtt,et al.  MOLECULAR BIOLOGY OF THE EXTRACELLULAR MATRIX PROTEINS , 1988, Biological reviews of the Cambridge Philosophical Society.

[53]  A. W. Schaefer,et al.  Galactosyl transferase-dependence of neurite outgrowth on substratum-bound laminin. , 1990, Development.

[54]  G W Plant,et al.  Neural tissue engineering: from polymer to biohybrid organs. , 1996, Biomaterials.

[55]  Richard O. Hynes,et al.  Integrins: Versatility, modulation, and signaling in cell adhesion , 1992, Cell.

[56]  S. Carbonetto Facilitatory and inhibitory effects of glial cells and extracellular matrix in axonal regeneration , 1991, Current Opinion in Neurobiology.

[57]  F. Rathjen Neural cell contact and axonal growth. , 1991, Current opinion in cell biology.

[58]  J. Silver,et al.  Postnatally induced formation of the corpus callosum in acallosal mice on glia-coated cellulose bridges. , 1983, Science.

[59]  C. Peschle,et al.  Astrocyte cultures from human embryonic brain: Characterization and modulation of surface molecules by inflammatory cytokines , 1992, Journal of neuroscience research.

[60]  K. Ulbrich,et al.  Synthetic Polymer Matrices for Neural Cell Transplantation , 1993, Cell transplantation.

[61]  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.

[62]  A. Harvey,et al.  Fetal tectal or cortical tissue transplanted into brachial lesion cavities in rats: Influence on the regrowth of host retinal axons , 1987, The Journal of comparative neurology.

[63]  S. Harper,et al.  Neurite outgrowth of spinal neurons on tissue sections of embryonic muscle is largely integrin dependent , 1993, Neuroscience Letters.

[64]  P. Aebischer,et al.  Neuronal cell attachment to fluorinated ethylene propylene films with covalently immobilized laminin oligopeptides YIGSR and IKVAV. II. , 1995, Journal of biomedical materials research.

[65]  K. Gotō,et al.  Synthesis and cell attachment activity of bioactive oligopeptides: RGD, RGDS, RGDV, and RGDT. , 1991, Journal of biomedical materials research.

[66]  S. Woerly,et al.  Intracerebral implantation of synthetic polymer/biopolymer matrix: a new perspective for brain repair. , 1990, Biomaterials.

[67]  A. Vaheri,et al.  Laminin is induced in astrocytes of adult brain by injury. , 1984, The EMBO journal.

[68]  H. Müller,et al.  Astroglia‐released neurite growth‐inducing activity for embryonic hippocampal neurons is associated with laminin bound in a sulfated complex and free fibronectin , 1989, Glia.

[69]  S. Woerly,et al.  Intracerebral Implantation of Ionic Synthetic Hydrogels: Effect of Polar Substrata on Astrocytosis and Axons , 1992, Journal of neural transplantation & plasticity.