Arkoudi Kalliopi, Yuan Yue, Cumine Antonia Pia, Dyer Carlene, Busch-Nentwich Elisabeth, Bravo Isabel, Feng Yi, Knight Robert D
Centre for Craniofacial and Regenerative Biology, King's College London, Guy's Hospital, London, UK.
Carl Zeiss Microscopy GmbH, Jena, Germany.
NPJ Regen Med. 2025 Jun 3;10(1):27. doi: 10.1038/s41536-025-00414-1.
Inflammatory cells are crucial regulators of infection and regeneration that actively migrate to affected tissues. NF-kB and TNF-alpha (TNFα) are master regulators of immune signalling, but their importance for immune cell migration is much less well understood. We have therefore investigated how NF-kB and TNFα regulate both macrophage function and behaviour in vivo using a zebrafish model of tissue repair. We show that NF-kB activity differentially regulates TNFα activity through Tnf receptors 1a and 1b to control macrophage responses to injury. Loss of NF-kB in macrophages results in elevated TNFα expression and results in more directional migration. Impaired NF-kB activity in macrophages perturbs tissue regeneration, causes increased proliferation, altered pro- and anti-inflammatory gene expression and delays fin regeneration. We identify a crucial role for NF-kB modulation of TNFα signaling to regulate macrophage responses to tissue injury, which are necessary for effective fin regeneration.
炎症细胞是感染和再生的关键调节因子,可主动迁移至受影响的组织。核因子-κB(NF-κB)和肿瘤坏死因子-α(TNF-α)是免疫信号的主要调节因子,但它们对免疫细胞迁移的重要性却鲜为人知。因此,我们利用斑马鱼组织修复模型,研究了NF-κB和TNF-α如何在体内调节巨噬细胞的功能和行为。我们发现,NF-κB活性通过肿瘤坏死因子受体1a和1b差异调节TNF-α活性,以控制巨噬细胞对损伤的反应。巨噬细胞中NF-κB的缺失会导致TNF-α表达升高,并导致更具方向性的迁移。巨噬细胞中NF-κB活性受损会扰乱组织再生,导致增殖增加、促炎和抗炎基因表达改变,并延迟鳍再生。我们确定了NF-κB对TNF-α信号的调节在调控巨噬细胞对组织损伤反应中的关键作用,而这对于有效的鳍再生是必要的。