Obesity and neuroinflammatory phenotype in mice lacking endothelial megalin
Abstract
Background: The multiligand receptor megalin controls the brain uptake of a number of ligands, including insulin and leptin. Despite the role of megalin in the transport of these metabolically relevant hormones, the role of megalin at the blood-brain-barrier (BBB) has not yet been explored in the context of metabolic regulation. Methods: Here we investigate the role of brain endothelial megalin in energy metabolism and leptin signaling using an endothelial cell-specific megalin deficient (EMD) mouse model. Results: We found megalin is important to protect mice from developing obesity and metabolic syndrome when mice are fed a normal chow diet. EMD mice developed neuroinflammation, by triggering several pro-inflammatory cytokines, displayed reduced neurogenesis and mitochondrial deregulation. Conclusions: These results implicate brain endothelial megalin expression in obesity-related metabolic changes through the leptin signaling pathway proposing a potential link between obesity and neurodegeneration.
Más información
Título según WOS: | ID WOS:000397145900003 Not found in local WOS DB |
Título de la Revista: | JOURNAL OF NEUROINFLAMMATION |
Volumen: | 14 |
Editorial: | BMC |
Fecha de publicación: | 2017 |
DOI: |
10.1186/s12974-017-0800-2 |
Notas: | ISI |