Comprehensive Analysis of the Immune and Stromal Compartments of the CNS in EAE Mice Reveal Pathways by Which Chloroquine Suppresses Neuroinflammation.
Rodolfo ThomeAlexandra BoehmLarissa Lumi Watanabe IshikawaGiacomo CasellaJaqueline MunhozBogoljub CiricGuang-Xian ZhangAbdolmohamad RostamiPublished in: Brain sciences (2020)
Multiple sclerosis (MS) and experimental autoimmune encephalomyelitis (EAE) are neuroinflammatory diseases of the central nervous system (CNS), where leukocytes and CNS resident cells play important roles in disease development and pathogenesis. The antimalarial drug chloroquine (CQ) has been shown to suppress EAE by modulating dendritic cells (DCs) and Th17 cells. However, the mechanism of action by which CQ modulates EAE is far from being elucidated. Here, we comprehensively analyzed the CNS of CQ and PBS-treated EAE mice to identify and characterize the cells that are affected by CQ. Our results show that leukocytes are largely modulated by CQ and have a reduction in the expression of inflammatory markers. Intriguingly, CQ vastly modulated the CNS resident cells astrocytes, oligodendrocytes (OLs) and microglia (MG), with the latter producing IL-10 and IL-12p70. Overall, our results show a panoramic view of the cellular components that are affect by CQ and provide further evidence that drug repurposing of CQ will be beneficial to MS patients.
Keyphrases
- induced apoptosis
- multiple sclerosis
- cell cycle arrest
- dendritic cells
- blood brain barrier
- signaling pathway
- end stage renal disease
- traumatic brain injury
- endoplasmic reticulum stress
- cell death
- poor prognosis
- ms ms
- type diabetes
- bone marrow
- adipose tissue
- peritoneal dialysis
- spinal cord injury
- lipopolysaccharide induced
- cognitive impairment
- dna methylation
- patient reported outcomes
- quality improvement
- pi k akt
- high fat diet induced
- drug induced