Department of Molecular Immunology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan; Laboratory of Molecular Immunology, Immunology Frontier Research Center (IFReC), Osaka University, Suita, Osaka 565-0871, Japan.
Department of Molecular Immunology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.
Immunity. 2023 Feb 14;56(2):307-319.e8. doi: 10.1016/j.immuni.2023.01.008. Epub 2023 Feb 2.
Gaucher disease (GD) is the most common lysosomal storage disease caused by recessive mutations in the degrading enzyme of β-glucosylceramide (β-GlcCer). However, it remains unclear how β-GlcCer causes severe neuronopathic symptoms, which are not fully treated by current therapies. We herein found that β-GlcCer accumulating in GD activated microglia through macrophage-inducible C-type lectin (Mincle) to induce phagocytosis of living neurons, which exacerbated Gaucher symptoms. This process was augmented by tumor necrosis factor (TNF) secreted from activated microglia that sensitized neurons for phagocytosis. This characteristic pathology was also observed in human neuronopathic GD. Blockade of these pathways in mice with a combination of FDA-approved drugs, minocycline (microglia activation inhibitor) and etanercept (TNF blocker), effectively protected neurons and ameliorated neuronopathic symptoms. In this study, we propose that limiting unrestrained microglia activation using drug repurposing provides a quickly applicable therapeutic option for fatal neuronopathic GD.
戈谢病(GD)是最常见的溶酶体贮积病,由β-葡萄糖脑苷脂(β-GlcCer)降解酶的隐性突变引起。然而,目前尚不清楚β-GlcCer 如何导致严重的神经病变症状,而这些症状目前的治疗方法无法完全治疗。我们在此发现,在 GD 中积累的β-GlcCer 通过巨噬细胞诱导 C 型凝集素(Mincle)激活小胶质细胞,诱导活神经元的吞噬作用,从而加重戈谢病的症状。来自活化小胶质细胞分泌的肿瘤坏死因子(TNF)增强了这一过程,使神经元对吞噬作用敏感。在人类神经病变性 GD 中也观察到了这种特征性病理学变化。用 FDA 批准的药物米诺环素(小胶质细胞激活抑制剂)和依那西普(TNF 阻滞剂)的组合在小鼠中阻断这些途径,可有效保护神经元并改善神经病变症状。在这项研究中,我们提出,通过药物再利用限制不受控制的小胶质细胞激活为致命性神经病变 GD 提供了一种快速适用的治疗选择。