KIF5A regulates axonal repair and time-dependent axonal transport of SFPQ granules and mitochondria in human motor neurons
Irune Guerra San Juan, Jessie Brunner, Kevin Eggan, Ruud F. Toonen, Matthijs Verhage
Abstract
Mutations in the microtubule-binding motor protein kinesin 5 A (KIF5A) are impacted in several adult-onset motor neuron diseases, including Amyotrophic Lateral Sclerosis, Spastic Paraplegia Type 10 and Charcot-Marie-Tooth Disease Type 2. While KIF5 family members transport a variety of cargos along axons, the specific cargos affected by KIF5A mutations remain poorly understood. Here, we generated KIF5A null mutant human motor neurons and analyzed the impact on axonal transport and motor neuron outgrowth and regeneration in vitro . KIF5A deficiency caused reduced neurite complexity in young neurons (DIV14) and defects in axonal regeneration. KIF5A deficiency did not affect neurofilament transport but impaired mitochondrial motility and anterograde speed at DIV42. Notably, KIF5A deficiency strongly reduced anterograde transport of splicing factor proline/glutamine-rich (SFPQ)-associated RNA granules in DIV42 axons. Hence, KIF5A plays a critical role in promoting axonal regrowth after injury and in driving the anterograde transport of mitochondria and especially SFPQ-associated RNA granules in mature neurons. • KIF5A expression increases in human motor neurons as KIF5B/C levels decline over time. • KIF5A is essential for promoting axonal regrowth after injury. • Loss of KIF5A disrupts anterograde transport of mitochondria and SFPQ RNA granules. • Neurofilament transport remains unaffected in KIF5A null motor neurons. • Transport deficits emerge in later stages, suggesting a developmental cargo dependence.