F. Grassi et al., THE DESENSITIZATION OF THE EMBRYONIC MOUSE MUSCLE ACETYLCHOLINE-RECEPTOR DEPENDS ON THE CELLULAR ENVIRONMENT, Pflugers Archiv, 430(5), 1995, pp. 787-794
The rate of desensitization of nicotinic acetylcholine (ACh) receptor
(nAChR), an important characteristic of nAChR function, was studied in
myotubes of the mouse C2C12 cell line at different times after fusion
, by measuring the decay of ACh-evoked currents (I-ACh) under various
patch-clamp configurations. We observed a progressive slowing of I-ACh
decay rate (half-decay time rose from about 0.5 s to over 5 s) in myo
tubes of increasing size (i.e. age) under all experimental conditions,
except in outside-out patches, when I-ACh decayed as fast as in the s
mallest myotubes. Single-channel conductance (about 35 pS) and open ti
me (about 3.5 ms), measured in outside-out and cell-attached patches,
were independent of myotube size. In Xenopus oocytes injected with pol
y(A(+))RNA extracted from C2C12 myoblasts or mature myotubes, I-ACh de
cay was about 50 times slower than in myotubes. Neither cAMP-dependent
nor diacylglycerol-dependent protein kinases, actin nor microtubule p
olymerization state influenced I-ACh decay. Our data indicate that the
cellular environment, but not readily dialysable cytosolic factors, m
arkedly influences the functional behaviour of nAChR.