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Neuronal contact upregulates astrocytic sphingosine-1-phosphate receptor 1 to coordinate astrocyte-neuron cross communication.

Glia (2021-12-28)
Sandeep K Singh, Tomasz Kordula, Sarah Spiegel
RESUMEN

Astrocytes, the most abundant glial cells in the mammalian brain, directly associate with and regulate neuronal processes and synapses and are important regulators of brain development. Yet little is known of the molecular mechanisms that control the establishment of astrocyte morphology and the bi-directional communication between astrocytes and neurons. Here we show that neuronal contact stimulates expression of S1PR1, the receptor for the bioactive sphingolipid metabolite sphingosine-1-phosphate (S1P), on perisynaptic astrocyte processes and that S1PR1 drives astrocyte morphological complexity and morphogenesis. Moreover, the S1P/S1PR1 axis increases neuronal contact-induced expression of astrocyte secreted synaptogenic factors SPARCL1 and thrombospondin 4 that are involved in neural circuit assembly. Our findings have uncovered new functions for astrocytic S1PR1 signaling in regulation of bi-directional astrocyte-neuron crosstalk at the nexus of astrocyte morphogenesis and synaptogenesis.

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Sigma-Aldrich
Anticuerpo anti-transportador del glutamato, glial, serum, Chemicon®
Sigma-Aldrich
Anticuerpo anti-molécula de adhesión neuronal L1, clon 324, clone 324, Chemicon®, from rat
Sigma-Aldrich
Anticuerpo anti-receptor 1 de la esfingosina 1-fosfato 1 (S1P1), clon 8B7.1, clone 8B7.1, from mouse