Metabolic stabilization of muscle nicotinic acetylcholine receptor by rapsyn

J Neurosci. 1999 Mar 15;19(6):1998-2007. doi: 10.1523/JNEUROSCI.19-06-01998.1999.

Abstract

Although the metabolic half-life of muscle endplate acetylcholine receptor (AChR) changes during development and after denervation in the adult, little is known about the molecular mechanisms that influence receptor stability. We have investigated the effect on AChR turnover of its interaction with rapsyn, a 43 kDa peripheral membrane protein that is closely associated with the AChR in muscle cells and is required for its clustering at endplates. Both in transfected COS cells and in cultured myotubes from rapsyn-negative and rapsyn-positive mice, we have found that the presence of rapsyn slows the turnover of AChRs by as much as twofold. The effect was similar for both embryonic (alpha2betadeltagamma) and adult (alpha2betadeltaepsilon) AChRs and for AChRs whose beta subunit lacked a putative tyrosine phosphorylation site. Neither colchicine nor cytochalasin D altered AChR turnover or prevented the rapsyn effect. Mutant rapsyn proteins whose N-terminal myristoylation signal was eliminated, or whose C terminus or zinc-finger domains were deleted, failed to change the rate of receptor turnover. Each of these mutations affects the association of the AChR with rapsyn, suggesting that AChR stability is altered by interaction between the two proteins. Our results suggest that, in addition to its role in AChR clustering, rapsyn also functions to metabolically stabilize the AChR.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence / genetics
  • Animals
  • COS Cells
  • Cytoskeleton / physiology
  • Mice
  • Molecular Sequence Data
  • Muscle Proteins / deficiency
  • Muscle Proteins / physiology*
  • Muscles / metabolism*
  • Phosphorylation
  • Receptor Aggregation / physiology
  • Receptors, Nicotinic / deficiency
  • Receptors, Nicotinic / genetics
  • Receptors, Nicotinic / metabolism*
  • Receptors, Nicotinic / physiology*
  • Transfection
  • Tyrosine / metabolism

Substances

  • Muscle Proteins
  • Receptors, Nicotinic
  • peripheral membrane protein 43K
  • Tyrosine