Axonal outgrowth was measured, as previously described [25]. Briefly, primary cortical neurons were harvested from pregnant (embryonic day 18) Wistar rats. A microfluidic chamber (Standard Neuron Device; Xona Microfluidics, Temecula, CA, http://xonamicrofluidics.com) was used to separate axons from neuronal soma [26]. The experimental groups were (a) control, no treatment; (b) +50% of DM-BMSC-conditioned medium; (c) +50% of miR-145+/+DM-BMSC-conditioned medium; and (d) +50% of miR-145−/−DM-BMSC-conditioned medium.
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