The myelin-associated glycoprotein (MAG) is localized in the periaxonal part of PNS and CNS myelin sheaths where it appears to be involved in glia-axon ineractions. The amount of MAG in Jimpy mice with a severe hypomyelination is reduced to 5% of the control level, but its apparent molecular weight is not higher than normal as had previously been described in Quaking and Grembler mice. Several types of monoclonal antibodies have now been identified that react with related carbohydrate epitopes in MAG and other glycoconjugates. These include: 1. several that were generated by MBDS in mice immunized with MAG; 2. HNK-1, that reacts with a subset of human lymphocytes; 3. 10C5, an antibody reacting with glycoproteins in melanoma, small cell lung carcinoma and other tumors of neuroectodermal origin; 4. L2, an antibody reacting with several proteins involved in cell-cell interactions including neural cell adhesion molecule (N-CAM); and 5. human monoclonal IgM in paraproteinemia associated with neuropathy. In addition to MAG, each of these antibodies reacts with glycolipids and 20 to 26 K dalton glycoproteins that are specific for the PNS. The principal glycolipid reacting with these antibodies is an unusual sulfated, glucoronic acid-containing sphingoglycolipid that had not previously been described. The carbohydrate epitopes in MAG and other glycoconjugates of nervous tissue that are shared with the immune system and various tumors of neuroectodermal origin may be relevant to demyelinating diseases. A number of patients with IgM paraproteinemia associated with neuropathy have been identified in which the IgM does not react with MAG but does react with other glycolipids, indicating that glycolipid antigens are frequent in neuropathy associated with IgM gammopathy. Relatively high levels of a proteolytic derivative of MAG, dMAG are present in all cerebrospinal fluids, but the amount does not correlate with active demyelination. A low level of anti-MAG antibodies was detected in the cerebrospinal fluid of multiple sclerosis patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Intramural Research (Z01)
Project #
1Z01NS001808-16
Application #
4696795
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
16
Fiscal Year
1985
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Quarles, Richard H (2007) Myelin-associated glycoprotein (MAG): past, present and beyond. J Neurochem 100:1431-48
Quarles, Richard H (2005) Comparison of CNS and PNS myelin proteins in the pathology of myelin disorders. J Neurol Sci 228:187-9
Marta, C B; Taylor, C M; Cheng, S et al. (2004) Myelin associated glycoprotein cross-linking triggers its partitioning into lipid rafts, specific signaling events and cytoskeletal rearrangements in oligodendrocytes. Neuron Glia Biol 1:35-46
Vaurs-Barriere, Catherine; Wong, Kondi; Weibel, Thais D et al. (2003) Insertion of mutant proteolipid protein results in missorting of myelin proteins. Ann Neurol 54:769-80
Hai, Mehreen; Muja, Naser; DeVries, George H et al. (2002) Comparative analysis of Schwann cell lines as model systems for myelin gene transcription studies. J Neurosci Res 69:497-508
Dashiell, Suzanne M; Tanner, Sandra L; Pant, Harish C et al. (2002) Myelin-associated glycoprotein modulates expression and phosphorylation of neuronal cytoskeletal elements and their associated kinases. J Neurochem 81:1263-72
Madhavarao, C N; Hammer, J A; Quarles, R H et al. (2002) A radiometric assay for aspartoacylase activity in cultured oligodendrocytes. Anal Biochem 308:314-9
Quarles, R H (2002) Myelin sheaths: glycoproteins involved in their formation, maintenance and degeneration. Cell Mol Life Sci 59:1851-71
Yim, S H; Hammer, J A; Quarles, R H (2001) Differences in signal transduction pathways by which platelet-derived and fibroblast growth factors activate extracellular signal-regulated kinase in differentiating oligodendrocytes. J Neurochem 76:1925-34
Franzen, R; Tanner, S L; Dashiell, S M et al. (2001) Microtubule-associated protein 1B: a neuronal binding partner for myelin-associated glycoprotein. J Cell Biol 155:893-8

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