Hereditary spastic paraplegias: membrane traffic and the motor pathway.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 21139634.
- Also identified by DOI 10.1038/nrn2946 and PMC identifier 5584382.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Voluntary movement is a fundamental way in which animals respond to, and interact with, their environment. In mammals, the main CNS pathway controlling voluntary movement is the corticospinal tract, which encompasses connections between the cerebral motor cortex and the spinal cord. Hereditary spastic paraplegias (HSPs) are a group of genetic disorders that lead to a length-dependent, distal axonopathy of fibres of the corticospinal tract, causing lower limb spasticity and weakness. Recent work aimed at elucidating the molecular cell biology underlying the HSPs has revealed the importance of basic cellular processes — especially membrane trafficking and organelle morphogenesis and distribution— in axonal maintenance and degeneration.
Medical subject headings
- Cell Membrane
- Efferent Pathways
- Spastic Paraplegia, Hereditary