Two mitogenic regions of myelin basic protein interact with different receptors to induce Schwann cell proliferation in a cAMP dependent process
✍ Scribed by S.-F. Tzeng; G. E. Deibler; T. J. Neuberger; Dr. G. H. DeVries
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 970 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Previous studies have shown that myelin basic protein (MBP) is mitogenic for Schwann cells (SCs) in the presence of elevated intracellular CAMP. Two mitogenic regions of MBP have been identified: one mitogenic region within the first 44 residues of the aminoterminus (1-44) and the other mitogenic region within the terminal 15 residues of the carboxyl end of the molecule (152-167). Unlike the mitogenic effect of a myelin enriched fraction (MEF), the mitogenic effect of MBP was not reduced by the addition of the lysosomal inhibitor, ammonium chloride. These data indicate that MBP causes SC proliferation by direct interaction of MBP with a surface receptor. Using Scatchard analysis of the binding of MBP to SCs, we report that treatment with forskolin does not cause the upregulation of receptors for MBP. Moreover, MBP blocks the cross-linking of 12'I-bFGF with two fibroblast growth factor (FGF) receptors having apparent molecular weights of 140 kDa and 120 kDa, respectively. Since neither TGF-P nor PDGF-BB displaced cell surface bound I2'I-MBP, we conclude that MBP binds to the FGF receptor rather than other growth factor receptors. Furthermore, only MBP,,, interacted with ganglioside GM1, whereas MBP,,,-,,, did not interact with this ganglioside. These results are consistent with the view that ganglioside GMl mediates the mitogenic effects of MBP,,,, while the FGF receptor mediates the mitogenic effect of MBP,,2-l,,. Intracellular cAMP of SCs was transiently increased after the addition of macrophage conditioned medium, suggesting that macrophages may produce factors in vivo which can transiently elevate intracellular cAMP levels, allowing a wave of SC proliferation in response to MBP-related mitogens.