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(Received for publication, March 28, 1996, and in revised form, June 26, 1996)
From Regeneron Pharmaceuticals, Inc., Tarrytown, New York
10591-6707
Despite the widespread use of polypeptide growth
factors as pharmacological agents, little is known about the extent to
which these molecules regulate their cognate cell surface receptors and
signal transduction pathways in vivo. We have addressed
this issue with respect to the neurotrophic molecule ciliary
neurotrophic factor (CNTF). Administration of CNTF in vivo
resulted in modest decreases in levels of CNTFR
Volume 271, Number 37,
Issue of September 13, 1996
pp. 22839-22846
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
NON-EQUIVALENCE WITH PHARMACOLOGICAL ACTIVITY
mRNA and protein
in skeletal muscle. CNTF causes the rapid tyrosine phosphorylation of
LIFR
and gp130 and the induction of the immediate-early gene,
tis11; injection of CNTF 3-7 h after an initial exposure
failed to re-stimulate these immediate-early responses, suggesting a
biochemical desensitization to CNTF not accounted for by decreased
receptor protein. To determine whether the desensitization of
immediate-early responses caused by CNTF resulted in a
functional desensitization, we compared the efficacy of
multiple daily injections versus a single daily dose of
CNTF in preventing the denervation-induced atrophy of skeletal muscle.
Surprisingly, injections of CNTF every 6 h, which falls within the
putative refractory period for biochemical responses, resulted in
efficacy equal to or greater than injections once daily. These results
suggest that although much of the CNTF signal transduction machinery is
down-regulated with frequent CNTF dosing, biological signals continue
to be recognized and interpreted by the cell.
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