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Association between chronic stress-induced structural abnormalities in Ranvier nodes and reduced oligodendrocyte activity in major depression

机译:慢性应激引起的Ranvier淋巴结结构异常与重度抑郁症少突胶质细胞活动减少之间的关联

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Repeated stressful events are associated with the onset of major depressive disorder (MDD). We previously showed oligodendrocyte (OL)-specific activation of the serum/glucocorticoid-regulated kinase (SGK)1 cascade, increased expression of axon-myelin adhesion molecules, and elaboration of the oligodendrocytic arbor in the corpus callosum of chronically stressed mice. In the current study, we demonstrate that the nodes and paranodes of Ranvier in the corpus callosum were narrower in these mice. Chronic stress also led to diffuse redistribution of Caspr and Kv 1.1 and decreased the activity in white matter, suggesting a link between morphological changes in OLs and inhibition of axonal activity. OL primary cultures subjected to chronic stress resulted in SGK1 activation and translocation to the nucleus, where it inhibited the transcription of metabotropic glutamate receptors (mGluRs). Furthermore, the cAMP level and membrane potential of OLs were reduced by chronic stress exposure. We showed by diffusion tensor imaging that the corpus callosum of patients with MDD exhibited reduced fractional anisotropy, reflecting compromised white matter integrity possibly caused by axonal damage. Our findings suggest that chronic stress disrupts the organization of the nodes of Ranvier by suppressing mGluR activation in OLs, and that specific white matter abnormalities are closely associated with MDD onset.
机译:重复的压力事件与重度抑郁症(MDD)的发作有关。我们以前显示血清/糖皮质激素调节激酶(SGK)1级联的少突胶质细胞(OL)特异性激活,轴突-髓磷脂粘附分子的表达增加以及在慢性应激小鼠的the体中少突胶质乔木的形成。在当前的研究中,我们证明了mice体中Ranvier的节和副节在这些小鼠中较窄。慢性应激还导致Caspr和Kv 1.1的弥散性重新分布,并降低了白质的活性,这表明OLs的形态变化与轴突活性抑制之间存在联系。遭受长期压力的OL原代培养物导致SGK1活化和易位至细胞核,从而抑制了代谢型谷氨酸受体(mGluRs)的转录。此外,慢性应激暴露会降低OLs的cAMP水平和膜电位。我们通过扩散张量成像显示,MDD患者的call体表现出降低的分数各向异性,反映出可能由轴突损伤引起的白质完整性受损。我们的发现表明,慢性应激通过抑制OL中的mGluR激活而破坏了Ranvier结的组织,并且特定的白质异常与MDD发作密切相关。

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