Heparin and heparan sulfate partially inhibit induction of acetylcholine receptor accumulation by nerve in Xenopus culture
Open Access
- 1 May 1989
- journal article
- research article
- Published by Society for Neuroscience in Journal of Neuroscience
- Vol. 9 (5) , 1555-1561
- https://doi.org/10.1523/jneurosci.09-05-01555.1989
Abstract
It has been demonstrated that ACh receptors in Xenopus nerve-muscle cultures migrate in the membrane to the nerve contact area during junction formation (Anderson et al., 1977) and that “diffusion trapping” is the major mechanism for nerve-induced receptor accumulation (Kidokoro and Brass, 1985; Kuromi et al., 1985; Kidokoro et al., 1986). A crucial remaining question is how the nerve induces the trap for randomly diffusing ACh receptors. In this study we examined the effect of various glycosaminoglycans in the culture medium on the nerve-induced receptor accumulation and found that heparin and heparan sulfate partially inhibited nerve-induced receptor accumulation, but similar molecules, chondroitin sulfate type A and type C, did not. By chemical modification of heparin we also showed that N-sulfate residues and a large-molecular-weight molecule are essential for this inhibitory effect. Heparin did not affect ACh receptor clustering (hot-spot formation) in myocytes cultured without nerve. By changing the time and duration of heparin application, we found that heparin was effective in inhibiting nerve-induced receptor accumulation only when it was present in the culture medium during the period that neurites are actively forming contact with muscle membrane.This publication has 3 references indexed in Scilit:
- Aggregates of acetylcholine receptors are associated with plaques of a basal lamina heparan sulfate proteoglycan on the surface of skeletal muscle fibers.The Journal of cell biology, 1983
- Acetylcholine receptors in regenerating muscle accumulate at original synaptic sites in the absence of the nerve.The Journal of cell biology, 1979
- Electrophoretic movement and localization of acetylcholine receptors in the embryonic muscle cell membraneNature, 1978