Acetylcholine receptor turnover in membranes of developing muscle fibers

Peter N. Devreotes, Douglas M. Fambrough

Research output: Contribution to journalArticlepeer-review

221 Scopus citations


[125I]mono-iodo-a-bungarotoxin is used as a specific marker in a description of acetylcholine receptor metabolism. It is concluded that acetylcholine receptors in the surface membranes of chick and rat myotubes developing in cell cultures have a half-life of 22-24 h. α-bungarotoxin (bound to a receptor which is removed from the membrane) is degraded to monoiodotyrosine which appears in the medium. Several observations are consistent with a model in which receptors or a-bun-garotoxin-receptor complexes are internalized and then degraded: (a) the rate of appearance of iodotyrosine does not reach its maximal rate until 90 min after α-bungarotoxin is bound to the surface receptors; (b) 2,4-dinitrophenol, reduced temperature, and cell disruption all inhibit the degradation process. The degradation of surface receptors is not coupled to the process by which receptors are incorporated into the membrane. Evidence suggests that receptors are incorporated into the surface membrane from a presynthesized set of receptors containing about 10% as many a-bungarotoxin binding sites as does the surface. Additionally, a third set of acetylcholine receptors is described containing about 30% as many binding sites as does the surface. These "hidden" receptors are not precursors yet are not readily accessible for binding of extracellular a-bungarotoxin. These findings are discussed in relation to both plasma membrane biosynthesis and control of chemosensitivity in developing and denervated skeletal muscle.

Original languageEnglish (US)
Pages (from-to)335-358
Number of pages24
JournalJournal of Cell Biology
Issue number2
StatePublished - May 1 1975

ASJC Scopus subject areas

  • Cell Biology


Dive into the research topics of 'Acetylcholine receptor turnover in membranes of developing muscle fibers'. Together they form a unique fingerprint.

Cite this