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Cerebellar astrocytes treated by thyroid hormone modulate neuronal proliferation

✍ Scribed by Flávia Carvalho Alcantara Gomes; Cecilia Garcia Maia; João Ricardo Lacerda De Menezes; Vivaldo Moura Neto


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
173 KB
Volume
25
Category
Article
ISSN
0894-1491

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✦ Synopsis


Thyroid hormones are important for neurogenesis and gliogenesis during brain development. We have previously demonstrated that triiodothyronine (T 3 ) treatment induced proliferation in primary culture astrocytes derived from the cerebellum of neonatal rats. Conditioned medium obtained from those T 3 -treated astrocytes (T 3 CM) mimicked the effect of hormonal treatment on these cells. Because neuron-glia interaction plays an important role in brain development, we tested the ability of such T 3 -glial CM to influence neuronal physiology. With that aim, neurons from 19-day embryonic cerebella were cultivated for 24 h in the presence of CM obtained from T 3 -treated cerebellar astrocytes. Interestingly, the cerebellar neuronal population increased by 60-80% in T 3 CM. Addition of 5 µM forskolin enhanced the responsiveness of cerebellar neurons to astrocytes T 3 CM, but it did not interfere with neuronal survival in control medium. Conversely, inhibition of adenylate cyclase by its specific inhibitor, SQ22536, reversed the T 3 CM effect on neurons. These data strongly suggest that cAMP signal transduction pathways might be implicated in such an event. Analysis of bromodeoxyuridil incorporation revealed that the increase in neuron number in T 3 CM was partially due to neuron proliferation, because the proliferation index was three times higher in T 3 CM than in control medium. Neutralizing antibody assays demonstrated that T 3 CM effects on neurons are due, at least in part, to the presence of tumor necrosis factor-␤ and epidermal growth factor. Thus, we report here a novel molecular mechanism of action of thyroid hormone on cerebellar neuronal cells: Thyroid hormone induces astrocytes to secrete growth factors that can interfere with neuronal proliferation via a paracrine pathway.


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