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1. Full Text NgR1 and NgR3 are receptors for chondroitin sulfate proteoglycans
by Dickendesher, Travis L and Baldwin, Katherine T and Mironova, Yevgeniya A and Koriyama, Yoshiki and Raiker, Stephen J and Askew, Kim L and Wood, Andrew and Geoffroy, Cédric G and Zheng, Binhai and Liepmann, Claire D and Katagiri, Yasuhiro and Benowitz, Larry I and Geller, Herbert M and Giger, Roman J
Nature Neuroscience, ISSN 1097-6256, 05/2012, Volume 15, Issue 5, pp. 703 - 712
In the adult mammalian CNS, chondroitin sulfate proteoglycans (CSPGs) and myelin-associated inhibitors (MAIs) stabilize neuronal structure and restrict... 
RETINAL GANGLION-CELLS | NEURITE GROWTH | AXON REGENERATION | OPTIC-NERVE REGENERATION | SPINAL-CORD-INJURY | TYROSINE-PHOSPHATASE-SIGMA | CORTICOSPINAL TRACT REGENERATION | NOGO RECEPTOR | OLIGODENDROCYTE-MYELIN GLYCOPROTEIN | FUNCTIONAL RECEPTOR | NEUROSCIENCES | Protein Binding - genetics | Embryo, Mammalian | Humans | Myelin Proteins - deficiency | Nerve Regeneration - physiology | Myelin-Associated Glycoprotein - genetics | Myelin-Associated Glycoprotein - metabolism | Ganglia, Spinal - cytology | Dose-Response Relationship, Drug | Tubulin - metabolism | Transfection | GPI-Linked Proteins - deficiency | Receptor-Like Protein Tyrosine Phosphatases, Class 4 - pharmacology | Protein Binding - drug effects | Optic Nerve Injuries - metabolism | Neurons - metabolism | Nogo Receptor 1 | Neurons - drug effects | Receptors, Tumor Necrosis Factor - genetics | Animals, Newborn | Receptors, Tumor Necrosis Factor - metabolism | Gene Expression Regulation - genetics | Cells, Cultured | Chondroitin Sulfate Proteoglycans - metabolism | Gene Expression Regulation - physiology | Rats | Receptors, Cell Surface - metabolism | Mutation - genetics | Myelin Proteins - genetics | GPI-Linked Proteins - metabolism | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Analysis of Variance | Central Nervous System - cytology | Receptors, Cell Surface - deficiency | Mice | Myelin Proteins - metabolism | GPI-Linked Proteins - genetics | Receptors, Cell Surface - genetics | Neuroplasticity | Physiological aspects | Proteoglycans | Research | Chondroitin
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2. Full Text Chondroitin sulfate proteoglycans in demyelinated lesions impair remyelination
by Lau, Lorraine W and Keough, Michael B and Haylock‐Jacobs, Sarah and Cua, Rowena and Döring, Axinia and Sloka, Scott and Stirling, David P and Rivest, Serge and Yong, V. Wee
Annals of Neurology, ISSN 0364-5134, 09/2012, Volume 72, Issue 3, pp. 419 - 432
Objective: Failure of remyelination is a critical impediment to recovery in multiple sclerosis (MS). Chondroitin sulfate proteoglycans (CSPGs) have been... 
CHRONIC MULTIPLE-SCLEROSIS | MYELIN | PROTEIN | CNS REMYELINATION | OLIGODENDROCYTE PROGENITOR MATURATION | GLIAL SCAR | SPINAL-CORD-INJURY | EXTRACELLULAR-MATRIX | NG2 PROTEOGLYCAN | DIFFERENTIATION | NEUROSCIENCES | CLINICAL NEUROLOGY | Humans | Nerve Regeneration - physiology | Demyelinating Diseases - metabolism | Glial Fibrillary Acidic Protein - metabolism | Chondroitin ABC Lyase - pharmacology | Chondroitin Sulfate Proteoglycans - pharmacology | Time Factors | Spinal Cord - pathology | Up-Regulation - physiology | Female | Demyelinating Diseases - chemically induced | Microfilament Proteins - metabolism | Indoles | Disease Models, Animal | Calcium-Binding Proteins - metabolism | Myelin Basic Protein - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | Cell Adhesion - drug effects | Glycosides - pharmacology | Up-Regulation - drug effects | Platelet-Derived Growth Factor - metabolism | Animals | Demyelinating Diseases - diet therapy | Analysis of Variance | Cell Differentiation - drug effects | Stem Cells - drug effects | Mice | In Vitro Techniques | Lysophosphatidylcholines - toxicity | Myelin Proteins - metabolism | Cell Line, Transformed | Glycosides - therapeutic use | Medical research | Multiple sclerosis | Chondroitin sulfate
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3. Full Text Chondroitin sulfate proteoglycans inhibit oligodendrocyte myelination through PTPσ
by Pendleton, James C and Shamblott, Michael J and Gary, Devin S and Belegu, Visar and Hurtado, Andres and Malone, Misti L and McDonald, John W
Experimental Neurology, ISSN 0014-4886, 09/2013, Volume 247, pp. 113 - 121
CNS damage often results in demyelination of spared axons due to oligodendroglial cell death and dysfunction near the injury site. Although new oligodendroglia... 
CSPG | Protein tyrosine phosphatase | Demyelination | Oligodendrocyte progenitor cell | Animals, Newborn | Myelin Basic Protein - metabolism | Cells, Cultured | Myelin Sheath - drug effects | Rats | Ganglia, Spinal - cytology | Chondroitin ABC Lyase - pharmacology | Rats, Sprague-Dawley | Gene Expression Regulation - drug effects | Stem Cells | Animals | Chondroitin Sulfate Proteoglycans - pharmacology | Oligodendroglia - drug effects | Proteoglycans - pharmacology | Signal Transduction - drug effects | rho-Associated Kinases - metabolism | Cell Differentiation - drug effects | Gangliosides - metabolism | Receptor-Like Protein Tyrosine Phosphatases, Class 2 - metabolism | Aggrecans - pharmacology | Neurofilament Proteins - metabolism | Antigens - pharmacology | RNA, Small Interfering - metabolism
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4. Full Text The inhibitory effects of chondroitin sulfate proteoglycans on oligodendrocytes
by Siebert, Justin R and Osterhout, Donna J
Journal of Neurochemistry, ISSN 0022-3042, 10/2011, Volume 119, Issue 1, pp. 176 - 188
J. Neurochem. (2011) 119, 176–188. The formation of the glial scar following a spinal cord injury presents a significant barrier to the regenerative process.... 
differentiation | progenitor cell | rho kinase | chondroitin sulfate proteoglycans | oligodendrocyte | VERSICAN | GLIAL SCAR | BIOCHEMISTRY & MOLECULAR BIOLOGY | AXONAL REGENERATION | CELL-ADHESION | NEUROSCIENCES | NEURITE OUTGROWTH | CLARKES NEURONS | IN-VIVO | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | Amides - pharmacology | Chondroitin ABC Lyase - chemistry | Immunohistochemistry | Cells, Cultured | Enzyme Inhibitors - pharmacology | Myelin Sheath - drug effects | Rats | Rats, Sprague-Dawley | rho-Associated Kinases - antagonists & inhibitors | Spinal Cord Injuries - pathology | Stem Cells | Animals | Chondroitin Sulfate Proteoglycans - pharmacology | Oligodendroglia - drug effects | Image Processing, Computer-Assisted | Proteoglycans - pharmacology | Signal Transduction - drug effects | rho-Associated Kinases - metabolism | Cell Adhesion - physiology | Cell Differentiation - drug effects | Pyridines - pharmacology | Sulfates | Analysis | Chondroitin | Neurochemistry | Spinal cord injuries | Cellular biology | Kinases
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5. Full Text Chondroitin sulfate proteoglycans: Key modulators in the developing and pathologic central nervous system
by Dyck, Scott M and Karimi-Abdolrezaee, Soheila
Experimental Neurology, ISSN 0014-4886, 07/2015, Volume 269, pp. 169 - 187
Chondroitin Sulfate Proteoglycans (CSPGs) are a major component of the extracellular matrix in the central nervous system (CNS) and play critical role in the... 
Multiple sclerosis | Intacellular mechanisms | Nervous system | Central | Glial scar | Spinal cord injury | Chondroitin sulfate proteoglycans | PTPσ | Axonal regeneration | Plasticity | Development | Extracellular matrix | LAR | TYROSINE-PHOSPHATASE RECEPTOR | OLIGODENDROCYTE PRECURSOR CELLS | PTP sigma | NEUROSCIENCES | NEURITE GROWTH | PTP-SIGMA | IMPROVES FUNCTIONAL RECOVERY | REACTIVE ASTROCYTES | SPINAL-CORD-INJURY | PROMOTES AXON GROWTH | EXTRACELLULAR-MATRIX | PERINEURONAL NETS | Animals | Central Nervous System - metabolism | Chondroitin Sulfate Proteoglycans - pharmacology | Spinal Cord Injuries - drug therapy | Brain Injuries - drug therapy | Humans | Nerve Regeneration - physiology | Chondroitin Sulfate Proteoglycans - metabolism | Nerve Regeneration - drug effects | Central Nervous System - drug effects | Neuronal Plasticity - drug effects | Sulfates | Chondroitin | Central nervous system
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6. Full Text Chondroitin sulfate proteoglycans in neural development and regeneration
by Laabs, Tracy and Carulli, Daniela and Geller, Herbert M and Fawcett, James W
Current Opinion in Neurobiology, ISSN 0959-4388, 2005, Volume 15, Issue 1, pp. 116 - 120
Proteoglycans are of two main types, chondroitin sulfate (CSPGs) and heparin sulfate (HSPGs). The CSPGs act mainly as barrier-forming molecules, whereas the... 
SENSORY AXONS | ASTROCYTE BOUNDARY | NEURITE OUTGROWTH | WHITE-MATTER | VISUAL-CORTEX | GLIAL SCAR | GROWTH | AXONAL REGENERATION | CENTRAL-NERVOUS-SYSTEM | SPINAL-CORD-INJURY | NEUROSCIENCES | Chondroitin Sulfate Proteoglycans - physiology | Animals | Humans | Nerve Regeneration - physiology | Neurons - physiology | Anticoagulants (Medicine) | Proteoglycans | Sulfates | Chondroitin
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7. Full Text Contributions of chondroitin sulfate proteoglycans to neurodevelopment, injury, and cancer
by Silver, Daniel J and Silver, Jerry
Current Opinion in Neurobiology, ISSN 0959-4388, 2014, Volume 27, pp. 171 - 178
Highlights • CSPGs mediate three distinct modes of cellular migration. • CSPGs can redirect, confine, or amplify cell migration. • CSPG structure, time,... 
Neurology | Psychiatry | PROTEOLYTIC CLEAVAGE | AXON GROWTH | NEURITE OUTGROWTH | INTEGRIN EXPRESSION | GLIAL SCAR | REGENERATION | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | EXTRACELLULAR-MATRIX | CELL | NEUROSCIENCES | Central Nervous System - growth & development | Neoplasms - metabolism | Chondroitin Sulfate Proteoglycans - physiology | Animals | Central Nervous System - metabolism | Central Nervous System - cytology | Models, Biological | Humans | Neurons - physiology | Neurons - metabolism | Cell Movement - physiology | Central Nervous System Diseases - metabolism | Sulfates | Cancer | Neurosciences | Mediation | Cell Migration | Glioma | CSPG Receptor | Brain Tumor | Glioblastoma | CSPG | Chondroitin Sulfate Proteoglycan | Glial Scar | Axon Guidance | LAR | Invasion
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8. Full Text Integrin activation promotes axon growth on inhibitory chondroitin sulfate proteoglycans by enhancing integrin signaling
by Tan, Chin Lik and Kwok, Jessica C.F and Patani, Rickie and Ffrench-Constant, Charles and Chandran, Siddharthan and Fawcett, James W
Journal of Neuroscience, ISSN 0270-6474, 04/2011, Volume 31, Issue 17, pp. 6289 - 6295
Chondroitin sulfate proteoglycans (CSPGs) are upregulated after CNS lesions, where they inhibit axon regeneration. In order for axon growth and regeneration to... 
NERVOUS-SYSTEM | DIVALENT-CATIONS | NEURITE OUTGROWTH | MECHANISM | PLATELET-AGGREGATION | GLIAL SCAR | REGENERATION | CELL-ADHESION MOLECULES | NEUROSCIENCES | AGGRECAN | TENASCIN-C | Humans | Male | Neurons - cytology | Axons - physiology | Ganglia, Spinal - cytology | Chondroitin ABC Lyase - pharmacology | Integrins - metabolism | Dose-Response Relationship, Drug | Drug Interactions | Time Factors | Aggrecans - pharmacology | Neurons - drug effects | Manganese - pharmacology | Integrins - immunology | Cells, Cultured | Chondroitin Sulfate Proteoglycans - metabolism | Axons - drug effects | Gene Expression Regulation - physiology | Rats | Rats, Sprague-Dawley | Lamins - pharmacology | Antibodies - pharmacology | Gene Expression Regulation - drug effects | Animals | Signal Transduction - drug effects | Signal Transduction - physiology | Neural Inhibition - drug effects | Brief Communications
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9. Full Text Perisynaptic chondroitin sulfate proteoglycans restrict structural plasticity in an integrin-dependent manner
by Orlando, Clara and Ster, Jeanne and Gerber, Urs and Fawcett, James W and Raineteau, Olivier
Journal of Neuroscience, ISSN 0270-6474, 12/2012, Volume 32, Issue 50, pp. 18009 - 18017
During early postnatal development of the CNS, neuronal networks are configured through the formation, elimination, and remodeling of dendritic spines, the... 
SLICE CULTURES | ADULT VISUAL-CORTEX | DENDRITIC SPINE MORPHOLOGY | EXTRACELLULAR-MATRIX | PERINEURONAL NETS | CELL-ADHESION | LONG-TERM POTENTIATION | SYNAPTIC PLASTICITY | NEUROSCIENCES | OCULAR DOMINANCE PLASTICITY | INTRACORTICAL INHIBITION | CA1 Region, Hippocampal - physiology | Focal Adhesion Protein-Tyrosine Kinases - metabolism | Chondroitin Sulfate Proteoglycans - metabolism | Dendritic Spines - physiology | Extracellular Matrix - metabolism | Blotting, Western | Extracellular Matrix - chemistry | Integrin beta1 - metabolism | Chondroitin ABC Lyase - metabolism | Microscopy, Confocal | Patch-Clamp Techniques | Animals | Neuronal Plasticity - physiology | Pyramidal Cells - physiology | Fluorescent Antibody Technique | Mice | Pyramidal Cells - ultrastructure | Organ Culture Techniques | CA1 Region, Hippocampal - ultrastructure | Dendritic Spines - ultrastructure
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10. Full Text Overcoming neurite‐inhibitory chondroitin sulfate proteoglycans in the astrocyte matrix
by Cua, Rowena C and Lau, Lorraine W and Keough, Michael B and Midha, Rajiv and Apte, Suneel S and Yong, V. Wee
Glia, ISSN 0894-1491, 06/2013, Volume 61, Issue 6, pp. 972 - 984
Acute trauma to the central nervous system (CNS) can result in permanent damage and loss of function related to the poor regeneration of injured axons. Injured... 
axonal regeneration | neurons | extracellular matrix | MMPs | proteases | Extracellular matrix | Neurons | Proteases | Axonal regeneration | WHITE-MATTER | AXON REGENERATION | METALLOPROTEINASE INHIBITORS | NEUROSCIENCES | PROMOTES FUNCTIONAL RECOVERY | MULTIPLE-SCLEROSIS | CNS INJURY | INTRACEREBRAL HEMORRHAGE | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | EXTRACELLULAR-MATRIX | Humans | Nerve Regeneration - physiology | Chondroitin Sulfate Proteoglycans - metabolism | Axons - metabolism | Extracellular Matrix - metabolism | Male | Neurites - metabolism | Brain - metabolism | Animals | Female | Mice | Matrix Metalloproteinases - metabolism | Astrocytes - metabolism | Sulfates | Chondroitin | Proteins | Medical research | Wound healing | Index Medicus
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11. Full Text Leukocyte common antigen-related phosphatase is a functional receptor for chondroitin sulfate proteoglycan axon growth inhibitors
by Fisher, Daniel and Xing, Bin and Dill, John and Li, Hui and Hoang, Hai Hiep and Zhao, Zhenze and Yang, Xiao-Li and Bachoo, Robert and Cannon, Stephen and Longo, Frank M and Sheng, Morgan and Silver, Jerry and Li, Shuxin
Journal of Neuroscience, ISSN 0270-6474, 10/2011, Volume 31, Issue 40, pp. 14051 - 14066
Chondroitin sulfate proteoglycans (CSPGs) are a family of extracellular matrix molecules with various functions in regulating tissue morphogenesis, cell... 
NEURAL DEVELOPMENT | RHOA INHIBITION | NEURITE OUTGROWTH | GLIAL SCAR | IN-VIVO | CONE COLLAPSE | PROTEIN-TYROSINE PHOSPHATASES | SPINAL-CORD-INJURY | CENTRAL-NERVOUS-SYSTEM | PROMOTES RECOVERY | NEUROSCIENCES | Axons - enzymology | Humans | Mice, Inbred C57BL | Cells, Cultured | Chondroitin Sulfate Proteoglycans - metabolism | Axons - drug effects | Axons - metabolism | Cercopithecus aethiops | Growth Inhibitors - metabolism | Mice, Knockout | Animals | Chondroitin Sulfate Proteoglycans - pharmacology | Mice, Mutant Strains | Female | Mice | COS Cells | Growth Inhibitors - pharmacology | Receptor-Like Protein Tyrosine Phosphatases, Class 2 - physiology | Protein Binding - physiology
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12. Full Text Chondroitin sulfate proteoglycans as novel drivers of leucocyte infiltration in multiple sclerosis
by Stephenson, Erin L and Mishra, Manoj K and Moussienko, Daniel and Laflamme, Nataly and Rivest, Serge and Ling, Chang-Chun and Yong, V Wee
Brain, ISSN 0006-8950, 04/2018, Volume 141, Issue 4, pp. 1094 - 1110
Perivascular cuffs are portals for leucocyte entry into CNS parenchyma. Stephenson et al. report that in a rodent model of multiple sclerosis and brain tissue... 
Perivascular cuff | Neuroinflammation | Multiple sclerosis | Chondroitin sulfate proteoglycans | Versican | T-CELL MIGRATION | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | multiple sclerosis | SPINAL-CORD | NEUROSCIENCES | CLINICAL NEUROLOGY | MEDICAL PROGRESS | neuroinflammation | chondroitin sulfate proteoglycans | P-SELECTIN | versican | CENTRAL-NERVOUS-SYSTEM | EXTRACELLULAR-MATRIX | PERINEURONAL NETS | perivascular cuff | MOLECULAR-MECHANISMS | BASEMENT-MEMBRANE | Tumor Necrosis Factor-alpha - metabolism | Freund's Adjuvant - toxicity | Peptide Fragments - toxicity | RNA, Messenger - metabolism | Myelin-Oligodendrocyte Glycoprotein - toxicity |