Journal of Neuroscience, Vol 14, 3620-3627, Copyright © 1994 by Society for Neuroscience
Androgenic regulation of tubulin gene expression in axotomized hamster facial motoneurons
KJ Jones and MM Oblinger
Department of Physical Therapy, University of Illinois at Chicago 60612.
We have previously demonstrated that systemic administration of
testosterone increases the rate of axonal regeneration following facial
nerve crush in adult male hamsters. In this investigation, the molecular
mechanisms by which androgens may enhance axonal regeneration were
examined. Specifically, the following question was addressed using Northern
blot and in situ hybridization with three cytoskeletal cDNA probes
complementary to beta II-, beta III-, and alpha 1-tubulin mRNA: does
exogenous testosterone augment axotomy-induced changes in tubulin mRNA
expression in hamster facial motoneurons (FMN)? Adult male hamsters were
subjected to unilateral facial nerve severance, with the opposite side
serving as an internal control. One-half of the animals were subcutaneously
implanted with Silastic capsules containing crystalline testosterone
propionate and the other half implanted with blank capsules. Postoperative
survival times were 2 and 7 d. At 2 d after axotomy alone, no changes in
levels of any of the three tubulin mRNAs were observed in the injured FMN.
However, by 7 d after axotomy, significant increases in all three tubulin
mRNAs were observed. This time course of axotomy-induced changes in tubulin
gene expression is consistent with findings in other injured neuronal
populations. Administration of testosterone at the time of injury had two
major effects on the cytoskeletal response pattern in axotomized FMN.
First, testosterone differentially regulated the set of tubulin mRNAs
examined, in that beta II-tubulin mRNA levels were selectively altered by
the steroid, whereas beta III- or alpha 1-tubulin mRNAs were not.(ABSTRACT
TRUNCATED AT 250 WORDS)