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首页> 外文期刊>Journal of Neuropathology and Experimental Neurology: Official Journal of the American Association of Neuropathologists, Inc >Neuron-conditioned media differentially affect the survival of activated or unstimulated microglia: evidence for neuronal control on apoptotic elimination of activated microglia.
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Neuron-conditioned media differentially affect the survival of activated or unstimulated microglia: evidence for neuronal control on apoptotic elimination of activated microglia.

机译:神经元条件培养基对激活的或未刺激的小胶质细胞的存活有不同的影响:凋亡消除激活的小胶质细胞的神经元控制的证据。

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It is presently unknown what types of neuronal signals maintain microglial cells resting in the normal brain or control their activation in neuropathology. Recent data suggest that microglia activation induces apoptosis and that healthy neurons are controllers of the activation state and immune functions of microglia. In the present study we have evaluated, on microglial cells in cultures, whether neurons are able to affect their survival in resting conditions or upon activation with the bacterial endotoxin, lipopolysaccharide (LPS). We report that neuron-conditioned culture media induced apoptosis of LPS-stimulated, but not of unstimulated, microglia. This effect was, however, only present when conditioned media had been exposed to differentiated neurons and not to immature ones, and was absent when glutamate receptors had been pharmacologically blocked in neuronal cultures. The effect was also blocked by heat-inactivation of the conditioned media. Media conditioned with either differentiated or undifferentiated cerebellar granule neurons positively affected the survival of unstimulated microglial cells when the standard concentration of fetal bovine serum (10%) was included in the culture media. Our results highlight the ability of differentiated neurons to maintain a controlled inflammatory state through production of factor(s) favoring the apoptotic elimination of activated microglia. They also suggest that immature neurons may, on the contrary, favor the survival of microglia during development.
机译:目前尚不清楚哪种神经元信号可以维持正常大脑中的小胶质细胞或控制其在神经病理学中的激活。最近的数据表明,小胶质细胞的激活会诱导细胞凋亡,而健康的神经元是小胶质细胞的激活状态和免疫功能的控制者。在本研究中,我们已经在培养物中的小胶质细胞上评估了神经元是否能够在静止条件下或在被细菌内毒素脂多糖(LPS)激活后影响其存活。我们报告说,神经元条件培养基诱导LPS刺激,但不是未刺激的小胶质细胞凋亡。但是,只有在条件培养基暴露于分化的神经元而不是未成熟的神经元的情况下,才会出现这种效应,而当谷氨酸受体的药理作用在神经元培养物中被阻断时,这种效应就不存在。通过条件培养基的热灭活也阻止了该作用。当标准浓度的胎牛血清(10%)包含在培养基中时,以分化的或未分化的小脑颗粒神经元为条件的培养基会积极影响未刺激的小胶质细胞的存活。我们的结果突出了分化神经元通过产生有利于凋亡消除活化小胶质细胞的因子来维持受控炎症状态的能力。他们还表明,相反,未成熟的神经元可能在发育过程中有利于小胶质细胞的存活。

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