Extracellular Matrix 2: Role of extracellular matrix molecules and their receptors in the nervous system

Extracellular matrix molecules help regulate many aspects of neural development, including survival, migration, axon growth, and synapse formation by neurons. These same molecules have been shown to modulate regeneration of neurons after injuries. They also regulate the development and differentiation of other neural cells, such as astroglia and Schwann cells. Significant progress has been made recently in characterizing both ECM constituents and their receptors in the nervous system. Extracellular matrix molecules promote cell adhesion, activate intracellular signaling pathways, and modulate the activities of several growth factors and proteins. Our current understanding of the extracellular matrix, its receptors, and its functions in the nervous system are discussed.—Venstrom, K. A., Reichardt, L. F. Role of extracellular matrix molecules and their receptors in the nervous system. FASEB J. 7: 996‐1003; 1993.

[1]  M. Waterfield,et al.  Glial growth factors are alternatively spliced erbB2 ligands expressed in the nervous system , 1993, Nature.

[2]  J. Lawler,et al.  Identification and characterization of thrombospondin-4, a new member of the thrombospondin gene family , 1993, Journal of Cell Biology.

[3]  R. Tucker The in situ localization of tenascin splice variants and thrombospondin 2 mRNA in the avian embryo. , 1993, Development.

[4]  E. Rozengurt,et al.  Focal adhesion kinase (p125FAK): A point of convergence in the action of neuropeptides, integrins, and oncogenes , 1992, Cell.

[5]  E. Ruoslahti,et al.  Natural inhibitor of transforming growth factor-β protects against scarring in experimental kidney disease , 1992, Nature.

[6]  K. Hayashi,et al.  Endothelial cells interact with the core protein of basement membrane perlecan through beta 1 and beta 3 integrins: an adhesion modulated by glycosaminoglycan , 1992, The Journal of cell biology.

[7]  L. Reichardt,et al.  Regulation of expression of fibronectin and its receptor, alpha 5 beta 1, during development and regeneration of peripheral nerve. , 1992, Development.

[8]  K. Crossin,et al.  Characterization of multiple adhesive and counteradhesive domains in the extracellular matrix protein cytotactin , 1992, The Journal of cell biology.

[9]  J. O’Rear A novel laminin B1 chain variant in avian eye. , 1992, Journal of Biological Chemistry.

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

[11]  L. Honig,et al.  Agrin isoforms and their role in synaptogenesis. , 1992, Current opinion in cell biology.

[12]  R. Falchetto,et al.  Neuronal cell adhesion molecule contactin/F11 binds to tenascin via its immunoglobulin-like domains , 1992, The Journal of cell biology.

[13]  P. Maurel,et al.  Cloning and primary structure of neurocan, a developmentally regulated, aggregating chondroitin sulfate proteoglycan of brain. , 1992, The Journal of biological chemistry.

[14]  K. Campbell,et al.  Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy , 1992, Nature.

[15]  S. Drake,et al.  A cell-surface heparan sulfate proteoglycan mediates neural cell adhesion and spreading on a defined sequence from the C-terminal cell and heparin binding domain of fibronectin, FN-C/H II , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  J. Sanes,et al.  Roles for the integrin VLA-4 and its counter receptor VCAM-1 in myogenesis , 1992, Cell.

[17]  P. Bornstein,et al.  Thrombospondin 3 (Thbs3), a new member of the thrombospondin gene family. , 1992, The Journal of biological chemistry.

[18]  S. Hockfield,et al.  The high molecular weight Cat-301 chondroitin sulfate proteoglycan from brain is related to the large aggregating proteoglycan from cartilage, aggrecan. , 1992, The Journal of biological chemistry.

[19]  F. Rathjen,et al.  The chicken neural extracellular matrix molecule restrictin: Similarity with EGF-, fibronectin type III-, and fibrinogen-like motifs , 1992, Neuron.

[20]  P. McGuire,et al.  Transforming growth factor-beta alters differentiation in cultures of avian neural crest-derived cells: effects on cell morphology, proliferation, fibronectin expression, and melanogenesis. , 1992, Developmental biology.

[21]  W. Song,et al.  H36-alpha 7 is a novel integrin alpha chain that is developmentally regulated during skeletal myogenesis [published erratum appears in J Cell Biol 1992 Jul;118(1):213] , 1992, The Journal of cell biology.

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

[23]  T. Jessell,et al.  F-spondin: A gene expressed at high levels in the floor plate encodes a secreted protein that promotes neural cell adhesion and neurite extension , 1992, Cell.

[24]  D. Carey,et al.  Molecular cloning and characterization of N-syndecan, a novel transmembrane heparan sulfate proteoglycan , 1992, The Journal of cell biology.

[25]  M. D. Murphy,et al.  S-laminin expression in adult and developing retinae: A potential cue for photoreceptor morphogenesis , 1992, Neuron.

[26]  O. Ibraghimov-Beskrovnaya,et al.  Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix , 1992, Nature.

[27]  F. W. Wolf,et al.  Characterization of mouse thrombospondin 2 sequence and expression during cell growth and development. , 1992, The Journal of biological chemistry.

[28]  T. Hardingham,et al.  Proteoglycans: many forms and many functions , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[29]  S. Schultz-Cherry,et al.  Transforming growth factor-beta complexes with thrombospondin. , 1992, Molecular biology of the cell.

[30]  H. Kresse,et al.  Peripheral distribution of dermatan sulfate proteoglycans (decorin) in amyloid-containing plaques and their presence in neurofibrillary tangles of Alzheimer's disease. , 1992, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[31]  E. Engvall,et al.  Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells. , 1992, Experimental cell research.

[32]  D. Templeton Proteoglycans in cell regulation. , 1992, Critical reviews in clinical laboratory sciences.

[33]  D. Noonan,et al.  The complete sequence of perlecan, a basement membrane heparan sulfate proteoglycan, reveals extensive similarity with laminin A chain, low density lipoprotein-receptor, and the neural cell adhesion molecule. , 1991, The Journal of biological chemistry.

[34]  A. Pearlman,et al.  Changes in the distribution of extracellular matrix components accompany early morphogenetic events of mammalian cortical development , 1991 .

[35]  M. Bernfield,et al.  Possible Regulation of FGF Activity by Syndecan, an Integral Membrane Heparan Sulfate Proteoglycan a , 1991, Annals of the New York Academy of Sciences.

[36]  N. Cashman,et al.  An LRE (leucine-arginine-glutamate)-dependent mechanism for adhesion of neurons to S-laminin , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  R. Weinberg,et al.  Expression cloning and characterization of the TGF-β type III receptor , 1991, Cell.

[38]  J. Massagué,et al.  Structure and expression of the membrane proteoglycan betaglycan, a component of the TGF-β receptor system , 1991, Cell.

[39]  A. Lander,et al.  Relationship between neuronal migration and cell-substratum adhesion: laminin and merosin promote olfactory neuronal migration but are anti- adhesive , 1991, The Journal of cell biology.

[40]  M. E. van der Rest,et al.  Collagen family of proteins , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[41]  J. Ervasti,et al.  Membrane organization of the dystrophin-glycoprotein complex , 1991, Cell.

[42]  R. Oppenheim,et al.  Immunolocalization studies of putative guidance molecules used by axons and growth cones of intersegmental interneurons in the chick embryo spinal cord , 1991, The Journal of comparative neurology.

[43]  R. Mecham Receptors for laminin on mammalian cells , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[44]  J. Prince,et al.  The primary structure of NG2, a novel membrane-spanning proteoglycan , 1991, The Journal of cell biology.

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

[46]  L. Reichardt,et al.  Vitronectin and thrombospondin promote retinal neurite outgrowth: Developmental regulation and role of integrins , 1991, Neuron.

[47]  Jeffrey D. Esko,et al.  Cell surface, heparin-like molecules are required for binding of basic fibroblast growth factor to its high affinity receptor , 1991, Cell.

[48]  L. Reichardt,et al.  Extracellular matrix molecules and their receptors: functions in neural development. , 1991, Annual review of neuroscience.

[49]  R. Timpl,et al.  Differential expression of laminin A and B chains during development of embryonic mouse organs. , 1990, Development.

[50]  M. Chiquet,et al.  Tenascin is accumulated along developing peripheral nerves and allows neurite outgrowth in vitro. , 1990, Development.

[51]  J. Sanes,et al.  Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere , 1990, The Journal of cell biology.

[52]  J. Sanes,et al.  Distribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunits. , 1990, Cell regulation.

[53]  M. Raff,et al.  Extracellular matrix-associated molecules collaborate with ciliary neurotrophic factor to induce type-2 astrocyte development , 1990, The Journal of cell biology.

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

[55]  V. Dixit,et al.  Deposition and role of thrombospondin in the histogenesis of the cerebellar cortex , 1990, The Journal of cell biology.

[56]  R. Perris,et al.  Inhibition of neural crest cell migration by aggregating chondroitin sulfate proteoglycans is mediated by their hyaluronan-binding region. , 1990, Developmental biology.

[57]  J. Spring,et al.  Two contrary functions of tenascin: Dissection of the active sites by recombinant tenascin fragments , 1989, Cell.

[58]  E. Ruoslahti,et al.  Multiple domains of the large fibroblast proteoglycan, versican. , 1989, The EMBO journal.

[59]  D. McClay,et al.  Cell adhesion to fibronectin and tenascin: quantitative measurements of initial binding and subsequent strengthening response , 1989, The Journal of cell biology.

[60]  E. Ruoslahti Proteoglycans in cell regulation. , 1989, Journal of Biological Chemistry.

[61]  H. Erickson,et al.  Tenascin: an extracellular matrix protein prominent in specialized embryonic tissues and tumors. , 1989, Annual review of cell biology.

[62]  V. Dixit,et al.  Unique distribution of the extracellular matrix component thrombospondin in the developing mouse embryo , 1988, The Journal of cell biology.

[63]  M. Lieberman,et al.  The neuronal cell-surface molecule mitogenic for Schwann cells is a heparin-binding protein. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[64]  M. Humphries,et al.  Neurite extension of chicken peripheral nervous system neurons on fibronectin: relative importance of specific adhesion sites in the central cell-binding domain and the alternatively spliced type III connecting segment , 1988, The Journal of cell biology.

[65]  M. Vigny,et al.  Heparan sulfate proteoglycan and laminin mediate two different types of neurite outgrowth , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.