期刊
NATURE
卷 549, 期 7672, 页码 389-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature23672
关键词
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资金
- NCI Cancer Center Support Grant (CCSG) [P30 CA08748]
- Cycle for Survival
- Marie-Josee and Henry R. Kravis Center for Molecular Oncology
- National Cancer Institute of the US National Institutes of Health [P30CA008748]
- MSKCC core grant
- Artemis Association/Histio (UK)/A.G. Leventis Foundation
- Ludwig Institute for Cancer Research
- NIH/NIAID [1R01AI130345-01]
- EMBO [ALTF 530-2015]
- Deutsche Krebshilfe e.V. [111354]
- American Society of Hematology
- Histiocytosis Association
- Erdheim-Chester Disease Global Alliance
- Pershing Square Sohn Cancer Foundation
- Leuekmia and Lymphoma Society
- NIH/NCI [R01 CA201247-01]
- BMBF
- Sobek-Foundation
- DFG [SFB 992, SFB1140, SFB/TRR167]
- Ministry of Science, Research and Arts, Baden-Wuerttemberg
The pathophysiology of neurodegenerative diseases is poorly understood and there are few therapeutic options. Neurodegenerative diseases are characterized by progressive neuronal dysfunction and loss, and chronic glial activation(1). Whether microglial activation, which is generally viewed as a secondary process, is harmful or protective in neurodegeneration remains unclear(1-8). Late-onset neurodegenerative disease observed in patients with histiocytoses(9-12), which are clonal myeloid diseases associated with somatic mutations in the RAS-MEK-ERK pathway such as BRAF(V600E)(13-17), suggests a possible role of somatic mutations in myeloid cells in neurodegeneration. Yet the expression of BRAF(V600E) in the haematopoietic stem cell lineage causes leukaemic and tumoural diseases but not neurodegenerative disease(18,19). Microglia belong to a lineage of adult tissue-resident myeloid cells that develop during organogenesis from yolk-sac erythro-myeloid progenitors (EMPs) distinct from haematopoietic stem cells(20-23). We therefore hypothesized that a somatic BRAF(V600E) mutation in the EMP lineage may cause neurodegeneration. Here we show that mosaic expression of BRAF(V600E) in mouse EMPs results in clonal expansion of tissue-resident macrophages and a severe late-onset neurodegenerative disorder. This is associated with accumulation of ERK-activated amoeboid microglia in mice, and is also observed in human patients with histiocytoses. In the mouse model, neurobehavioural signs, astrogliosis, deposition of amyloid precursor protein, synaptic loss and neuronal death were driven by ERK-activated microglia and were preventable by BRAF inhibition. These results identify the fetal precursors of tissue-resident macrophages as a potential cell-of-origin for histiocytoses and demonstrate that a somatic mutation in the EMP lineage in mice can drive late-onset neurodegeneration. Moreover, these data identify activation of the MAP kinase pathway in microglia as a cause of neurodegeneration and this offers opportunities for therapeutic intervention aimed at the prevention of neuronal death in neurodegenerative diseases.
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