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Expression of nerve growth factor precursor, mature nerve growth factor and their receptors during cerebral ischemia-reperfusion injury

机译:神经生长因子前体,成熟神经生长因子及其受体在脑缺血再灌注损伤中的表达

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We investigated nerve growth factor precursor (proNGF) and mature NGF expression in ischemic and non-ischemic cortices after cerebral ischemia-reperfusion injury. In both ischemic and non-ischemic cortices, proNGF was found to be present in the extracellular space and cytoplasm. In addition, mature NGF was expressed in extracellular space, but with a very low signal. In ischemic cortex only, proNGF was significantly decreased, reaching a minimal level at 1 day. Mature NGF was increased at 4 hours, then reached a minimal level at 3 days. The p75 neurotrophin receptor (p75 NTR ) was significantly decreased after ischemia, and increased at 3 days after ischemia. These results confirmed that proNGF was the predominant form of NGF during the pathological process of cerebral ischemia-reperfusion injury. In addition, our findings suggest that ischemic injury may influence the conversion of proNGF to mature NGF, and that proNGF/p75 NTR may be involved in reperfusion injury.
机译:我们调查了脑缺血再灌注损伤后缺血和非缺血性皮层神经生长因子前体(proNGF)和成熟的NGF表达。在缺血性和非缺血性皮层中,都发现proNGF存在于细胞外空间和细胞质中。另外,成熟的NGF在细胞外空间表达,但信号非常低。仅在缺血皮层中,proNGF显着降低,在1天时达到最低水平。成熟的NGF在4小时时增加,然后在3天时达到最低水平。缺血后p75神经营养蛋白受体(p75 NTR )显着降低,缺血3天后升高。这些结果证实,proNGF是脑缺血-再灌注损伤的病理过程中NGF的主要形式。此外,我们的发现提示缺血性损伤可能影响proNGF向成熟NGF的转化,而proNGF / p75 NTR 可能与再灌注损伤有关。

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