PF4通过CXCR3/PI3K/AKT/Nrf2途径调控脑出血中神经元的铁凋亡

0 MEDICINE, RESEARCH & EXPERIMENTAL Biomolecules & biomedicine Pub Date : 2025-04-26 DOI:10.17305/bb.2024.11415
Na Hu, Yunfeng Li, Guohong Zhang, Wei Wang, Liping An, Ran An, Yu Liu
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摘要

抑制高铁血症是治疗脑内出血(ICH)引起的神经元损伤的一种很有前景的策略。血小板因子 4(PF4)是一种具有多种生物功能的趋化因子,它在 ICH 中的作用及其对神经元铁嗜性的影响尚不清楚。为了研究这个问题,我们在体外 PC12 细胞中建立了血素诱导的损伤模型,并通过静脉注射胶原酶在体内建立了 ICH 模型。血液素处理过的 PC12 细胞与重组小鼠 PF4(Rm-PF4)蛋白共同培养,以研究 PF4 对铁突变的影响。此外,给 ICH 小鼠腹腔注射 Rm-PF4,评估其对神经功能障碍、脑水肿和神经元铁蛋白沉积的影响。研究人员采用了 Western 印迹分析法来评估 PF4 水平、CXCR3/PI3K/AKT/Nrf2 通路激活情况以及与铁突变相关的蛋白表达。结果发现,在 ICH 小鼠血肿周围脑组织和血清素处理的 PC12 细胞中,PF4 水平都有所降低。使用 Rm-PF4 治疗可降低亚铁离子、MDA 和 ROS 水平,从而有效抑制 PC12 细胞中的铁突变。此外,Rm-PF4 还能缓解 ICH 小鼠的神经功能障碍、神经元损伤和脑水肿,同时抑制神经元的铁卟啉沉积。从机理上讲,Rm-PF4 激活了 CXCR3/PI3K/AKT/Nrf2 通路,而 CXCR3 拮抗剂会减弱 ICH 小鼠和血清素处理 PC12 细胞的这种保护作用。总之,PF4通过激活CXCR3/PI3K/AKT/Nrf2通路,减轻了小鼠模型和PC12细胞中ICH诱导的神经元铁突变。
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PF4 regulates neuronal ferroptosis in cerebral hemorrhage through CXCR3/PI3K/AKT/Nrf2 pathway.

Inhibiting ferroptosis represents a promising strategy for managing neuronal injury caused by intracerebral hemorrhage (ICH). Platelet factor 4 (PF4), a chemokine with diverse biological functions, has an unclear role in ICH and its impact on neuronal ferroptosis. To investigate this, a hemin-induced injury model was established in PC12 cells in vitro, and an ICH model was created in vivo using IV collagenase injection. Hemin-treated PC12 cells were co-cultured with recombinant mouse PF4 (Rm-PF4) protein to examine the effects of PF4 on ferroptosis. Additionally, Rm-PF4 was administered intraperitoneally to ICH mice, and its influence on neurological dysfunction, brain edema, and neuronal ferroptosis was evaluated. Western blot analysis was employed to assess PF4 levels, CXCR3/phosphatidylinositol 3-kinase (PI3K)/AKT/nuclear factor erythroid-2-related factor 2 (Nrf2) pathway activation, and ferroptosis-related protein expression. PF4 levels were found to be reduced in both perihematomal brain tissues of ICH mice and hemin-treated PC12 cells. Treatment with Rm-PF4 decreased ferrous ion, malondialdehyde (MDA), and reactive oxygen species (ROS) levels, effectively inhibiting ferroptosis in PC12 cells. Furthermore, Rm-PF4 administration alleviated neurological dysfunction, neuronal damage, and brain edema while suppressing neuronal ferroptosis in ICH mice. Mechanistically, Rm-PF4 activated the CXCR3/PI3K/AKT/Nrf2 pathway, and this protective effect was diminished by a CXCR3 antagonist in both ICH mice and hemin-treated PC12 cells. In conclusion, PF4 mitigates ICH-induced neuronal ferroptosis in mouse models and PC12 cells by activating the CXCR3/PI3K/AKT/Nrf2 pathway.

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