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Leptin reverses corticosterone-induced inhibition of neural stem cell proliferation through activating the NR2B subunits of NMDA receptors. | LitMetric

AI Article Synopsis

  • Corticosterone is known to inhibit the growth of neural stem cells (NSCs) in the hippocampus, but removing this inhibition can help with neural regeneration. * Leptin, a hormone tied to brain development and neural health, was found to enhance the proliferation of NSCs and counteract corticosterone's inhibitory effects in a way that depends on its concentration. * The effects of leptin on NSCs proliferation involve increasing the expression of NR2B, a subunit of NMDA receptors, and certain antagonists can block these beneficial effects of leptin, indicating a complex relationship between these molecules.

Article Abstract

Corticosterone inhibits the proliferation of hippocampal neural stem cells (NSCs). The removal of corticosterone-induced inhibition of NSCs proliferation has been reported to contribute to neural regeneration. Leptin has been shown to regulate brain development, improve angiogenesis, and promote neural regeneration; however, its effects on corticosterone-induced inhibition of NSCs proliferation remain unclear. Here we reported that leptin significantly promoted the proliferation of hippocampal NSCs in a concentration-dependent pattern. Also, leptin efficiently reversed the inhibition of NSCs proliferation induced by corticosterone. Interestingly, pre-treatment with non-specific NMDA antagonist MK-801, specific NR2B antagonist Ro 25-6981, or small interfering RNA (siRNA) targeting NR2B, significantly blocked the effect of leptin on corticosterone-induced inhibition of NSCs proliferation. Furthermore, corticosterone significantly reduced the protein expression of NR2B, whereas pre-treatment with leptin greatly reversed the attenuation of NR2B expression caused by corticosterone in cultured hippocampal NSCs. Our findings demonstrate that leptin reverses the corticosterone-induced inhibition of NSCs proliferation. This process is, at least partially mediated by increased expression of NR2B subunits of NMDA receptors.

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Source
http://dx.doi.org/10.1016/j.bbrc.2014.03.112DOI Listing

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