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Involvement of the Tyro3 receptor and its intracellular partner Fyn signaling in Schwann cell myelination

机译:Tyro3受体及其胞内伴侣Fyn信号传导参与雪旺氏细胞髓鞘形成

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During early development of the peripheral nervous system, Schwann cell precursors proliferate, migrate, and differentiate into premyelinating Schwann cells. After birth, Schwann cells envelop neuronal axons with myelin sheaths. Although some molecular mechanisms underlying myelination by Schwann cells have been identified, the whole picture remains unclear. Here we show that signaling through Tyro3 receptor tyrosine kinase and its binding partner, Fyn nonreceptor cytoplasmic tyrosine kinase, is involved in myelination by Schwann cells. Impaired formation of myelin segments is observed in Schwann cell neuronal cultures established from Tyro3-knockout mouse dorsal root ganglia (DRG). Indeed, Tyro3-knockout mice exhibit reduced myelin thickness. By affinity chromatography, Fyn was identified as the binding partner of the Tyro3 intracellular domain, and activity of Fyn is down-regulated in Tyro3-knockout mice, suggesting that Tyro3, acting through Fyn, regulates myelination. Ablating Fyn in mice results in reduced myelin thickness. Decreased myelin formation is observed in cultures established from Fyn-knockout mouse DRG. Furthermore, decreased kinase activity levels and altered expression of myelination-associated transcription factors are observed in these knockout mice. These results suggest the involvement of Tyro3 receptor and its binding partner Fyn in Schwann cell myelination. This constitutes a newly recognized receptor-linked signaling mechanism that can control Schwann cell myelination.
机译:在周围神经系统的早期发育过程中,雪旺氏细胞前体增殖,迁移并分化为前髓鞘性雪旺氏细胞。出生后,雪旺氏细胞将髓鞘包裹神经元轴突。尽管已经确定了雪旺氏细胞髓鞘形成的一些分子机制,但整个情况仍不清楚。在这里,我们显示通过Tyro3受体酪氨酸激酶及其结合伴侣Fyn非受体胞质酪氨酸激酶发出的信号参与了施旺细胞的髓鞘形成。在从Tyro3敲除小鼠背根神经节(DRG)建立的Schwann细胞神经元培养物中观察到髓磷脂节段的形成受损。实际上,Tyro3基因敲除小鼠的髓磷脂厚度降低。通过亲和色谱,Fyn被确定为Tyro3细胞内结构域的结合伴侣,并且在Tyro3-敲除小鼠中Fyn的活性被下调,表明Tyro3通过Fyn起作用,可调节髓鞘形成。消除小鼠的Fyn可使髓鞘厚度减少。从Fyn基因敲除小鼠DRG建立的培养物中观察到髓磷脂形成减少。此外,在这些基因敲除小鼠中观察到激酶活性水平降低和髓鞘相关转录因子表达的改变。这些结果表明Tyro3受体及其结合伴侣Fyn参与了施旺细胞的髓鞘形成。这构成了一种新认识到的受体连锁信号传导机制,可以控制雪旺氏细胞的髓鞘形成。

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