Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann–Pick C1, Npc1

It has long been known that there is decreased mitochondrial function in several tissues of Niemann–Pick C1 model mice and cultured cells. These defects contribute to the accumulation of Reactive Oxygen Species (ROS) and tissue damage. It is also well established that there is increased unesterified cholesterol, stored in late endosomes/lysosomes, in many tissues in mutant humans, mouse models, and mutant cultured cells. Using a mouse model with...