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首页> 外文期刊>Journal of neuroinflammation >Astrocytes play a key role in activation of microglia by persistent Borna disease virus infection
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Astrocytes play a key role in activation of microglia by persistent Borna disease virus infection

机译:持续性的博尔纳病病毒感染,星形胶质细胞在激活小胶质细胞中起关键作用

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Neonatal Borna disease virus (BDV) infection of the rat brain is associated with microglial activation and damage to certain neuronal populations. Since persistent BDV infection of neurons is nonlytic in vitro, activated microglia have been suggested to be responsible for neuronal cell death in vivo. However, the mechanisms of activation of microglia in neonatally BDV-infected rat brains remain unclear. Our previous studies have shown that activation of microglia by BDV in culture requires the presence of astrocytes as neither the virus nor BDV-infected neurons alone activate microglia. Here, we evaluated the mechanisms whereby astrocytes can contribute to activation of microglia in neuron-glia-microglia mixed cultures. We found that persistent infection of neuronal cells leads to activation of uninfected astrocytes as measured by elevated expression of RANTES. Activation of astrocytes then produces activation of microglia as evidenced by increased formation of round-shaped, MHCI-, MHCII- and IL-6-positive microglia cells. Our analysis of possible molecular mechanisms of activation of astrocytes and/or microglia in culture indicates that the mediators of activation may be soluble heat-resistant, low molecular weight factors. The findings indicate that astrocytes may mediate activation of microglia by BDV-infected neurons. The data are consistent with the hypothesis that microglia activation in the absence of neuronal damage may represent initial steps in the gradual neurodegeneration observed in brains of neonatally BDV-infected rats.
机译:大鼠大脑的新生儿博尔纳病病毒(BDV)感染与小胶质细胞激活和某些神经元群体的损害有关。由于神经元的持续BDV感染在体外是非溶解性的,因此已建议活化的小胶质细胞负责体内神经元细胞的死亡。但是,新生的BDV感染的大鼠脑中小胶质细胞的激活机制仍不清楚。我们以前的研究表明,在培养物中通过BDV激活小胶质细胞需要存在星形胶质细胞,因为病毒和BDV感染的神经元都不能单独激活小胶质细胞。在这里,我们评估了星形胶质细胞可以促进神经胶质-小胶质细胞-小胶质细胞混合培养中的小胶质细胞活化的机制。我们发现神经元细胞的持续感染导致未感染的星形胶质细胞的活化,这通过提高RANTES的表达来衡量。星形胶质细胞的激活然后产生小胶质细胞的激活,如圆形,MHCI-,MHCII-和IL-6阳性小胶质细胞的形成增加所证明。我们对培养中星形胶质细胞和/或小胶质细胞活化的可能分子机制的分析表明,活化的介体可能是可溶性耐热的低分子量因子。这些发现表明星形胶质细胞可能通过BDV感染的神经元介导小胶质细胞的激活。数据与以下假设相符:无神经元损伤的情况下小胶质细胞活化可能代表了在新生BDV感染的大鼠的大脑中观察到的渐进性神经变性的初始步骤。

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