Yun Qian, Zhiwen Yan, Tianbao Ye, Victor Shahin, Jia Jiang, Cunyi Fan
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引用次数: 0
摘要
ATP 合成酶抑制因子 1(ATPIF1)是 ATP 合成酶复合物活性的一个关键调节因子,与各种生理和病理过程都有关系。虽然 ATPIF1 在缺氧、缺血再灌注损伤、细胞凋亡和癌症等情况下的作用已被确定,但它在周围神经再生中的参与仍然难以捉摸。本研究利用 ATPIF1 基因敲除转基因小鼠,揭示了 ATPIF1 的缺失会阻碍神经结构的重建,导致感觉和功能的延迟恢复。RNA测序揭示了外周神经损伤后免疫反应的显著减弱,这归因于CCR2/CCL2信号轴,并导致巨噬细胞浸润和活化的减少。重要的是,巨噬细胞而不是许旺细胞被确定为导致 ATPIF1 基因敲除小鼠沃勒氏变性延迟的关键因素,并影响周围神经再生的整体结果。这些结果揭示了 ATPIF1 在改善周围神经再生方面的转化潜力。
Decoding the regulatory role of ATP synthase inhibitory factor 1 (ATPIF1) in Wallerian degeneration and peripheral nerve regeneration
ATP synthase inhibitory factor 1 (ATPIF1), a key modulator of ATP synthase complex activity, has been implicated in various physiological and pathological processes. While its role is established in conditions such as hypoxia, ischemia‐reperfusion injury, apoptosis, and cancer, its involvement remains elusive in peripheral nerve regeneration. Leveraging ATPIF1 knockout transgenic mice, this study reveals that the absence of ATPIF1 impedes neural structural reconstruction, leading to delayed sensory and functional recovery. RNA‐sequencing unveils a significant attenuation in immune responses following peripheral nerve injury, which attributes to the CCR2/CCL2 signaling axis and results in decreased macrophage infiltration and activation. Importantly, macrophages, not Schwann cells, are identified as key contributors to the delayed Wallerian degeneration in ATPIF1 knockout mice, and affect the overall outcome of peripheral nerve regeneration. These results shed light on the translational potential of ATPIF1 for improving peripheral nerve regeneration.