Protein involved in hereditary spastic paraplegia influences lipids in muscle and brain
Tiny balls of fat blobbing around your cells, long thought to be basic fat storage devices, are in fact subtle masters of processes from energy supply to infection. The location of these lipid droplets is important, not least because they can cause disease when out of place. Researchers investigating their positioning in cells of people with hereditary spastic paraplegia may have found what directs them. Spastin is a protein that, when mutated, causes hereditary spastic paraplegia. Looking at cells with this mutation, researchers found that spastin (red, left) distribution in the cell coordinates endoplasmic reticulum (a structure involved in processing proteins, green) growth along structural microtubules (pink). Lipid droplet positioning relies on this machinery, and since spastin also guides other molecules involved, problems arise when it misfires. Any changes to the lipid landscape can cause the disease, and understanding this process might help develop new markers for diagnosis and treatment.
Written by
BPoD stands for Biomedical Picture of the Day. Managed by the MRC Laboratory of Medical Sciences until Jul 2023, it is now run independently by a dedicated team of scientists and writers. The website aims to engage everyone, young and old, in the wonders of biology, and its influence on medicine. The ever-growing archive of more than 4000 research images documents over a decade of progress. Explore the collection and see what you discover. Images are kindly provided for inclusion on this website through the generosity of scientists across the globe.
BPoD is also available in Catalan at www.bpod.cat with translations by the University of Valencia.