Murray Caroline E, Betancourt-Trompa David S, Martinez Michael S, Carson Julia M, Walsh Lindsay J, Remillard Will C, Fordyce Kayla B, Reddy Rohan, Soto Ileana
Department of Biology, Providence College, Providence, Rhode Island, United States of America.
Department of Biology, Brown University, Providence, Rhode Island, United States of America.
PLoS One. 2025 Sep 5;20(9):e0330437. doi: 10.1371/journal.pone.0330437. eCollection 2025.
In Npc1 deficient mice, postnatal developmental alterations in cerebellar microglia and Purkinje cells (PCs) are followed by early-onset neurodegeneration. Even in the absence of PC loss, microglia in Npc1nmf164 mice display hallmark features of activation during early postnatal development, including increased proliferation, enhanced phagocytic activity, and morphological changes indicative of an activated state. In this study, we investigated whether mammalian target of rapamycin complex 1 (mTORC1) drives postnatal activation of cerebellar microglia in Npc1nmf164 mice. We found that elevated CLEC7A (Dectin-1) expression and phosphorylation of S6 ribosomal protein (pS6R), a downstream target of mTORC1, co-occurred in microglial precursors within the developing white matter region (dWMR) of wild-type (WT) mice at postnatal day 7 (P7), as well as in neurodegeneration-associated microglia located in the molecular layer (ML) of Npc1nmf164 mice at P60. In contrast, microglia in the WMR of Npc1nmf164 mice at P60 did not show evidence of CLEC7A expression or increased mTORC1 activation. Interestingly, microglial precursors in the dWMR of Npc1nmf164 mice did not exhibit increased mTORC1 activation at P7 but instead showed delayed increased activation at P10. Inhibiting mTORC1 signaling with rapamycin from P10 to P21 reduced both microglial proliferation and soma size in Npc1nmf164 mice. Additionally, rapamycin treatment preserved VGLUT2⁺ presynaptic terminals/axons that innervate PC dendrites and decreased the total volume of CD68⁺ phagosomes per microglial cell, suggesting a reduction in phagocytic activity. However, the volume of VGLUT2⁺ synaptic material per phagosome remained unchanged between vehicle- and rapamycin-treated groups. While rapamycin enhanced myelination in Npc1nmf164 mice, it did not alter microglial phenotypes in the cerebellar WMR, suggesting that mTORC1 signaling does not mediate WMR microglial activation in this model. Together, our findings demonstrate that mTORC1 activation contributes to the aberrant activation of postnatal ML microglia and to early cerebellar pathology in Npc1nmf164 mice.
在Npc1基因缺陷小鼠中,小脑小胶质细胞和浦肯野细胞(PCs)的出生后发育改变随后会出现早发性神经变性。即使在没有PCs丢失的情况下,Npc1nmf164小鼠中的小胶质细胞在出生后早期发育过程中也表现出激活的标志性特征,包括增殖增加、吞噬活性增强以及形态变化,这些变化表明处于激活状态。在本研究中,我们调查了雷帕霉素复合物1(mTORC1)是否驱动Npc1nmf164小鼠小脑小胶质细胞的出生后激活。我们发现,在出生后第7天(P7)的野生型(WT)小鼠发育中的白质区域(dWMR)内的小胶质细胞前体中,以及在P60的Npc1nmf164小鼠分子层(ML)中的神经变性相关小胶质细胞中,CLEC7A(Dectin-1)表达升高和mTORC1的下游靶点S6核糖体蛋白(pS6R)的磷酸化同时出现。相比之下,P60时Npc1nmf164小鼠WMR中的小胶质细胞没有显示出CLEC7A表达或mTORC1激活增加的证据。有趣的是,Npc1nmf164小鼠dWMR中的小胶质细胞前体在P7时没有表现出mTORC1激活增加,而是在P10时显示出延迟的激活增加。从P10到P21用雷帕霉素抑制mTORC1信号传导可减少Npc1nmf164小鼠中的小胶质细胞增殖和细胞体大小。此外,雷帕霉素治疗保留了支配PC树突的VGLUT2⁺突触前终末/轴突,并减少了每个小胶质细胞中CD68⁺吞噬体的总体积,表明吞噬活性降低。然而,在载体处理组和雷帕霉素处理组之间,每个吞噬体中VGLUT2⁺突触物质的体积保持不变。虽然雷帕霉素增强了Npc1nmf164小鼠的髓鞘形成,但它并没有改变小脑WMR中的小胶质细胞表型,这表明在该模型中mTORC1信号传导不介导WMR小胶质细胞的激活。总之,我们的研究结果表明,mTORC1激活促成了Npc1nmf164小鼠出生后ML小胶质细胞的异常激活和早期小脑病理变化。