Lysosomal cholesterol accumulation in aged astrocytes impairs cholesterol delivery to neurons and can be rescued by cannabinoids

被引:6
|
作者
Allende, Leandro G. [1 ]
Natali, Lautaro [2 ]
Cragnolini, Andrea B. [3 ]
Bollo, Mariana [2 ]
Musri, Melina M. [2 ]
de Mendoza, Diego [4 ]
Martin, Mauricio G. [1 ]
机构
[1] Univ Nacl Cordoba, Dept Neurobiol Mol & celular, Inst Ferreyra, INIMEC CONICET UNC, Cordoba, Argentina
[2] Univ Nacl Cordoba, Dept Bioquim & Biofis, Inst Ferreyra, INIMEC CONICET UNC, Cordoba, Argentina
[3] Univ Nacl Cordoba, Fac Ciencias Exactas Fis & Nat, CONICET UNC, Inst Invest Biol & Tecnol, Cordoba, Argentina
[4] Univ Nacl Rosario, Inst Biol Mol & Celular Rosario IBR, Lab Fisiol Microbiana, Fac Ciencias Bioquim & Farmaceut,CONICET, Rosario, Argentina
关键词
aging; astrocytes; cannabinoids; cholesterol; trafficking; CENTRAL-NERVOUS-SYSTEM; LONG-TERM DEPRESSION; HIPPOCAMPAL; EXOCYTOSIS; METABOLISM; TRIGGERS; RELEASE; STRESS;
D O I
10.1002/glia.24580
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cholesterol is crucial for the proper functioning of eukaryotic cells, especially neurons, which rely on cholesterol to maintain their complex structure and facilitate synaptic transmission. However, brain cells are isolated from peripheral cholesterol by the blood-brain barrier and mature neurons primarily uptake the cholesterol synthesized by astrocytes for proper function. This study aimed to investigate the effect of aging on cholesterol trafficking in astrocytes and its delivery to neurons. We found that aged astrocytes accumulated high levels of cholesterol in the lysosomal compartment, and this cholesterol buildup can be attributed to the simultaneous occurrence of two events: decreased levels of the ABCA1 transporter, which impairs ApoE-cholesterol export from astrocytes, and reduced expression of NPC1, which hinders cholesterol release from lysosomes. We show that these two events are accompanied by increased microR-33 in aged astrocytes, which targets ABCA1 and NPC1. In addition, we demonstrate that the microR-33 increase is triggered by oxidative stress, one of the hallmarks of aging. By coculture experiments, we show that cholesterol accumulation in astrocytes impairs the cholesterol delivery from astrocytes to neurons. Remarkably, we found that this altered transport of cholesterol could be alleviated through treatment with endocannabinoids as well as cannabidiol or CBD. Finally, according to data demonstrating that aged astrocytes develop an A1 phenotype, we found that cholesterol buildup is also observed in reactive C3+ astrocytes. Given that reduced neuronal cholesterol affects synaptic plasticity, the ability of cannabinoids to restore cholesterol transport from aged astrocytes to neurons holds significant implications in aging and inflammation. Aged astrocytes with A1 phenotype accumulate cholesterol, decreasing its transport to neurons. microR-33 upregulation by oxidative stress leads to cholesterol accumulation. Cholesterol buildup is alleviated by cannabinoids rescuing its transport to neurons. image
引用
收藏
页码:1746 / 1765
页数:20
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