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Sox2 expression in Schwann cells inhibits myelination in vivo and induces influx of macrophages to the nerve

机译:雪旺细胞中Sox2的表达在体内抑制髓鞘形成并诱导巨噬细胞流入神经

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摘要

Correct myelination is crucial for the function of the peripheral nervous system. Both positive and negative regulators within the axon and Schwann cell function to ensure the correct onset and progression of myelination during both development and following peripheral nerve injury and repair. The Sox2 transcription factor is well known for its roles in the development and maintenance of progenitor and stem cell populations, but has also been proposed in vitro as a negative regulator of myelination in Schwann cells. We wished to test fully whether Sox2 regulates myelination in vivo and show here that, in mice, sustained Sox2 expression in vivo blocks myelination in the peripheral nerves and maintains Schwann cells in a proliferative non-differentiated state, which is also associated with increased inflammation within the nerve. The plasticity of Schwann cells allows them to re-myelinate regenerated axons following injury and we show that re-myelination is also blocked by Sox2 expression in Schwann cells. These findings identify Sox2 as a physiological regulator of Schwann cell myelination in vivo and its potential to play a role in disorders of myelination in the peripheral nervous system.
机译:正确的髓鞘形成对于周围神经系统的功能至关重要。轴突和雪旺氏细胞内的正负调节剂均起作用,以确保在发育以及周围神经损伤和修复后髓鞘的正确发作和进展。 Sox2转录因子因其在祖细胞和干细胞群体的发育和维持中的作用而广为人知,但在体外也被提议作为Schwann细胞中髓鞘形成的负调节剂。我们希望充分测试Sox2是否在体内调节髓鞘形成,并在此表明,在小鼠中,持续的Sox2表达在体内能阻断周围神经的髓鞘形成并使雪旺细胞保持增生的未分化状态,这也与体内炎症增加有关。神经。雪旺氏细胞的可塑性使它们能够在损伤后重新髓鞘再生再生的轴突,并且我们表明,雪旺氏细胞中Sox2的表达也能阻止髓鞘再生。这些发现将Sox2鉴定为体内雪旺氏细胞髓鞘形成的生理调节剂,并具有在周围神经系统髓鞘形成疾病中发挥作用的潜力。

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