Noradrenaline acting on astrocytic β2-adrenoceptors induces neurite outgrowth in primary cortical neurons

The neurotransmitter noradrenaline (NA) has anti-inflammatory properties and promotes expression of neurotrophic factors in the central nervous system (CNS) via activation of glial adrenoceptors. Here we examined the ability of conditioned media (CM) from NA-treated glial cells to impact upon neuron...

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Veröffentlicht in:Neuropharmacology 2014-02, Vol.77, p.234-248
Hauptverfasser: Day, Jennifer S., O'Neill, Eimear, Cawley, Caroline, Aretz, Nicholas Kruseman, Kilroy, Dana, Gibney, Sinead M., Harkin, Andrew, Connor, Thomas J.
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Sprache:eng
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Zusammenfassung:The neurotransmitter noradrenaline (NA) has anti-inflammatory properties and promotes expression of neurotrophic factors in the central nervous system (CNS) via activation of glial adrenoceptors. Here we examined the ability of conditioned media (CM) from NA-treated glial cells to impact upon neuronal complexity. Primary rat cortical neurons were treated either directly with NA (1–10 μM), or treated with CM from NA-stimulated primary mixed glial cells. Neuronal complexity was assessed using Sholl analysis. Exposure of neurons to CM from NA-stimulated glial cells increased all indices of neuronal complexity, whereas direct exposure of neurons to NA did not. CM from NA-stimulated astrocytes, but not microglia, also increased neuronal complexity indicating a key role for astrocytes. The β-adrenergic subtype was implicated in this response as the increase was blocked by the β-adrenoceptor antagonist propanolol, but not by the α-adrenoceptor antagonist phentolamine. CM from glial cells treated with the β2-adrenoceptor agonists salmeterol and clenbuterol, but not the β1-adrenoceptor agonist xamoterol, mimicked the ability of NA to increase neuronal complexity. NA induced expression of a range of growth factors (BDNF, NGF-β, GDNF, FGF-2 and IL-6) in glial cells. In addition to this, the phosphatidylinositol 3-kinase (PI3K), mitogen activated protein kinase (MAPK) and JAK-STAT signalling pathways are implicated in NA CM-induced neuritic growth as inhibition of these pathways attenuated NA CM-induced neuritic growth. In conclusion, this study indicates a novel role for NA acting at glial β2-adrenoceptors to induce neuritic growth through the expression of soluble factors that elicit a neurotrophic action and increase neuronal complexity. •Conditioned media from norarenaline-stimulated astrocytes induces neurite outgrowth.•β2-adrenoceptor stimulation on astrocytic cells promotes neurite outgrowth.•Growth factors mediate noradrenaline conditioned media induced neuritic growth.
ISSN:0028-3908
1873-7064
DOI:10.1016/j.neuropharm.2013.09.027