NCAM-Mediated Adhesion of Transfected Cells to Agrin

References

• Bayne E. K., Anderson M. J., Fambrough D. M. Extracellular matrix organization in developing muscle: correlation with acetylcholine receptor aggregates. J. Cell Biol. 1984; 99: 1486–1501
   PubMed Web of Science ®Google Scholar
• Burg M. A., Halfter W., Cole G. J. Analysis of proteoglycan expression in developing chicken brain: characterization of a heparan sulfate proteoglycan that interacts with the neural cell adhesion molecule. J. Neurosci. Res. 1995; 41: 49–64
   PubMed Web of Science ®Google Scholar
• Cashman N. R., Covault J., Wollman R. L., Sanes J. R. Neural cell adhesion molecule in normal, denervated, and myopathic human muscle. Annals Neurol. 1987; 21: 481–489
   PubMed Web of Science ®Google Scholar
• Cole G. J., Glaser L. A heparin-binding domain from NCAM is involved in neural cell-substratum adhesion. J. Cell Biol. 1986; 102: 403–412
   PubMed Web of Science ®Google Scholar
• Cole G. J., Burg M. Characterization of a heparan sulfate proteoglycan that copurifies with the neural cell adhesion molecule. Exp. Cell Res. 1989; 182: 44–60
   PubMed Web of Science ®Google Scholar
• Cole G. J., Schubert D., Glaser L. Cell-substratum adhesion in chick neural retina depends upon protein-hepa-ran sulfate interactions. J. Cell Biol. 1985; 100: 1192–1199
   PubMed Web of Science ®Google Scholar
• Cole G. J., Loewy A., Glaser L. Neuronal cell-cell adhesion depends on interactions of N-CAM with heparin-like molecules. Nature 1986; 320: 445–447
   PubMed Web of Science ®Google Scholar
• Covault J, Sanes J. R. Distribution of N-CAM in synaptic and extrasynaptic portions of developing and adult skeletal muscle. J. Cell Biol. 1986; 102: 716–730
   PubMed Web of Science ®Google Scholar
• Cunningham B. A., Hemperly J. J., Murray B. A., Prediger E., Brackenbury R., Edelman G. M. Neural cell adhesion molecule: Structure, immunoglobulin-like domains, cell surface modulation, and alternative RNA splicing. Science 1987; 236: 799–806
   PubMed Web of Science ®Google Scholar
• Fallon J. R., Nitkin R. M., Reist N. E., Wallace B. G., McMahan J. J. Acetylcholine receptor-aggregating factor is similar to molecules concentrated at neuromuscular junctions. Nature 1985; 315: 571–574
   PubMed Web of Science ®Google Scholar
• Fraser S. E., Murray B. A., Chuong C. M., Edelman G. M. Alterations of the retinotectal map in Xenopusby antibodies to neural cell adhesion molecules. Proc. Natl. Acad. Sci. USA 1984; 81: 4222–4226
   PubMed Web of Science ®Google Scholar
• Friedlander D. R., Milev P., Karthikeyan L., Margolis R. K., Margolis R. U., Grumet M. The neuronal chon-droitin sulfate proteoglycan neurocan binds to the neural cell adhesion molecules Ng-CAM/L1/NILE and N-CAM and inhibitis neuronal adhesion and neurite outgrowth. J. Cell Biol. 1994; 125: 669–680
   PubMed Web of Science ®Google Scholar
• Grumet M., Rutishauser U., Edelman G. M. Neural cell adhesion molecule is on embryonic muscle cells and mediates adhesion to nerve cells in vitro. Nature 1982; 295: 693–695
   PubMed Web of Science ®Google Scholar
• Grumet M., Flaccus A., Margolis R. U. Functional characterization of chondroitin sulfate proteoglycans of brain: interactions with neurons and neural cell adhesion molecules. J. Cell Biol. 1993; 120: 815–824
   PubMed Web of Science ®Google Scholar
• Halfter W. A heparan sulfate proteoglycan in developing avian axonal tracts. J. Neurosci. 1993; 13: 2863–2873
   PubMed Web of Science ®Google Scholar
• Halfter W., Schurer B. A new heparan sulfate proteoglycan in the extracellular matrix of the developing chick embryo. Exp. Cell Res. 1994; 214: 285–296
   PubMed Web of Science ®Google Scholar
• Hoffman S., Sorkin B. C., White P. C., Brackenbury R., Mail-hammer R., Rutishauser U., Cunningham B. A., Edelman G. M. Chemical characterization of a neural cell adhesion molecule purified from embryonic brain membranes. J. Biol. Chan. 1982; 257: 7720–7729
   PubMed Web of Science ®Google Scholar
• Kallapur S. G., Akeson R. A. The neural cell adhesion molecule (N-CAM) heparin binding domain binds to cell surface heparan sulfate proteoglycans. J. Neurosci. Res. 1992; 33: 538–548
   PubMed Web of Science ®Google Scholar
• Keilhauer G., Faissner A., Schachner M. Differential inhibition of neurone-neurone, neurone-astrocyte and astrocyte-astrocyte adhesion by L1, L2 and NCAM antibodies. Nature 1985; 316: 728–730
   PubMed Web of Science ®Google Scholar
• Lagenaur C., Lemmon V. An L1-like molecule, the 8D9 antigen, is a potent substrate for neurite extension. Proc. Natl. Acad. Sci. USA 1987; 84: 7753–7757
   PubMed Web of Science ®Google Scholar
• Milev P., Friedlander D. R., Sakurai T., Karthikeyan L., Flad M., Margolis R. K., Grumet M., Margolis R. U. Interactions of the chondroitin sulfate proteoglycan phosphacan, the extracellular domain of a receptor-type tyrosine phosphatase, with neurons, glia, and neural cell adhesion molecules. J. Cell Biol. 1994; 127: 1703–1715
   PubMed Web of Science ®Google Scholar
• Murray B. A., Jensen J. J. Evidence for heterophilic adhesion of embryonic retinal cells and neuroblastoma cells to substratum-adsorbed NCAM. J. Cell Biol. 1992; 117: 1311–1320
   PubMed Web of Science ®Google Scholar
• Nastuk M. A., Fallon J. R. Agrin and the molecular choreography of synapse formation. Trends Neurosci. 1993; 16: 72–76
   PubMed Web of Science ®Google Scholar
• Nitkin R. M., Smith M. A., Magill C., Fallon J. R., Yao Y. M., Wallace B. G., McMahan U. J. Identification of agrin, a synaptic organizing protein from Torpedo electric organ. J. Cell Biol. 1987; 105: 2471–2478
   PubMed Web of Science ®Google Scholar
• Rieger F., Grumet M., Edelman G. M. N-CAM at the vertebrate neuromuscular junction. J. Cell Biol. 1985; 101: 285–293
   PubMed Web of Science ®Google Scholar
• Reist N. E., Magill C., McMahan U. J. Agrin-like molecules at synaptic sites in normal, denervated, and damaged skeletal muscles. J. Cell Biol. 1987; 105: 2457–2469
   PubMed Web of Science ®Google Scholar
• Reyes A. A., Akeson R., Brezina L., Cole G. J. Structural requirements for neural cell adhesion molecule-heparin interaction. Cell Reg. 1990; 1: 567–576
   PubMedGoogle Scholar
• Sadoul R., Hirn M., Deagostini-Bazin H., Rougon G., Goridis C. Adult and embryonic mouse neural cell adhesion molecules have different binding properties. Nature 1983; 304: 347–349
   PubMed Web of Science ®Google Scholar
• Schubert D., LaCorbiere M. Role of a 16S glycoprotein complex in cellular adhesion. Proc. Natl. Acad. Sci. USA 1980; 77: 4137–4141
   PubMed Web of Science ®Google Scholar
• Schubert D., LaCorbiere M. The specificity of extracellular glycoprotein complexes in mediating cellular adhesion. J. Neurosci. 1982a; 2: 82–89
   PubMed Web of Science ®Google Scholar
• Schubert D., LaCorbiere M. Properties of extracellular adhesion-mediating particles in myoblast clone and its adhesion-deficient variant. J. Cell Biol. 1982b; 94: 108–114
   PubMed Web of Science ®Google Scholar
• Schubert D., LaCorbiere M., Klier F. G., Birdwell C. A role for adherons in neural retina cell adhesion. J. Cell Biol. 1983; 96: 990–998
   PubMed Web of Science ®Google Scholar
• Smith M. A., Yao Y. M., Reist N. E., Magill C., Wallace B. G., McMahan U. J. Identification of agrin in electric organ extracts and localization of agrin-like molecules in muscle and central nervous system. J. Exp. Biol. 1987; 132: 223–230
   PubMed Web of Science ®Google Scholar
• Storms S. D., Jensen J. J., Yaghmai D., Murray B. A. Multiple mechanisms of N2A and CHO cell adhesion to NCAM purified from chick embryonic brain and retina. Exp. Cell Res. 1994; 214: 100–112
   PubMed Web of Science ®Google Scholar
• Storms S. D., Anvekar V. M., Adams L. D., Murray B. A. Heterophilic NCAM-mediated adhesion to proteoglycans from chick embryonic brain membranes. Exp. Cell Res. 1996, in press
   PubMed Web of Science ®Google Scholar
• Tsen G., Halfter W., Kroger S., Cole G. J. Agrin is a heparan sulfate proteoglycan. J. Biol. Chem. 1995; 270: 3392–3399
   PubMed Web of Science ®Google Scholar
• Wallace B. G. Aggregating factor from Torpedo electric organ induces patches containing acetylcholine receptors, acetylcholinesterase, and butyrylcholinesterase on cultured myorubes. J. Cell Biol. 1986; 102: 783–794
   PubMed Web of Science ®Google Scholar
• Wallace B. G., Nitkin R. M., Reist N. E., Fallon J. R., Moayeri N. N., McMahan U. J. Aggregates of acetylcholinesterase induced by acetylcholine receptor-aggregating factor. Nature 1985; 315: 574–577
   PubMed Web of Science ®Google Scholar