Androgens regulate the physiology of motor neurones both during development
and in adult life. In particular, androgens increase the rate of axonal re
generation after axotomy, an effect correlated with the up-regulation of tu
bulin. In order to determine whether this was the result of a direct hormon
e action on neurones, we examined the effect of testosterone on microtubula
r proteins in human neuroblastoma SH-SY5Y cells. Treatment of proliferating
SH-SY5Y cells with testosterone resulted in an up-regulation of alpha- and
beta -tubulin. By contrast, no change in tubulin was observed either in ce
lls differentiated into a neuronal phenotype by retinoic acid or in adrenal
SW13 cells. We also show that an up-regulation of the ubiquitous beta (II)
-tubulin and of the neurone-specific beta (III)-tubulin isoforms contribute
s to the overall increase in tubulin in response to androgen treatment. The
increase in tubulin levels following testosterone treatment was abolished
by co-incubation with antiandrogens, indicating that this effect is, mediat
ed through a classical mechanism of steroid action. The two microtubule-ass
ociated proteins, tau and MAP2b, remained unchanged following testosterone
exposure. Thus, these results demonstrate that tubulin is a direct neuronal
target of androgen regulation and suggest that dysregulation of tubulin ex
pression may contribute to the pathogenesis of some motor neuronopathies.