UK Dementia Research Institute at The University of Edinburgh, Edinburgh, UK.
Centre for Discovery Brain Sciences, Chancellor's Building, The University of Edinburgh, Edinburgh, UK.
Nature. 2023 Jan;613(7942):120-129. doi: 10.1038/s41586-022-05534-y. Epub 2022 Dec 14.
Myelin is required for the function of neuronal axons in the central nervous system, but the mechanisms that support myelin health are unclear. Although macrophages in the central nervous system have been implicated in myelin health, it is unknown which macrophage populations are involved and which aspects they influence. Here we show that resident microglia are crucial for the maintenance of myelin health in adulthood in both mice and humans. We demonstrate that microglia are dispensable for developmental myelin ensheathment. However, they are required for subsequent regulation of myelin growth and associated cognitive function, and for preservation of myelin integrity by preventing its degeneration. We show that loss of myelin health due to the absence of microglia is associated with the appearance of a myelinating oligodendrocyte state with altered lipid metabolism. Moreover, this mechanism is regulated through disruption of the TGFβ1-TGFβR1 axis. Our findings highlight microglia as promising therapeutic targets for conditions in which myelin growth and integrity are dysregulated, such as in ageing and neurodegenerative disease.
髓鞘对于中枢神经系统神经元轴突的功能至关重要,但支持髓鞘健康的机制尚不清楚。尽管中枢神经系统中的巨噬细胞与髓鞘健康有关,但尚不清楚涉及哪些巨噬细胞群以及它们影响哪些方面。在这里,我们表明,在成年小鼠和人类中,驻留的小胶质细胞对于维持髓鞘健康至关重要。我们证明,小胶质细胞对于发育中的髓鞘包绕是可有可无的。然而,它们对于随后的髓鞘生长和相关认知功能的调节,以及通过防止髓鞘退化来维持髓鞘完整性是必需的。我们表明,由于小胶质细胞缺失导致的髓鞘健康丧失与脂质代谢改变的髓鞘形成少突胶质细胞状态的出现有关。此外,这种机制是通过破坏 TGFβ1-TGFβR1 轴来调节的。我们的发现强调了小胶质细胞作为治疗条件的有希望的治疗靶点,这些条件中髓鞘的生长和完整性受到干扰,例如在衰老和神经退行性疾病中。