Fast axonal transport is crucial for neuronal function and is driven by kinesins and cytoplasmic dynein. We investigated the role of the kinesin-1 motor complex in dense core vesicle (DCV) transport in C. elegans , using mutants in kinesin light chains ( klc -1 and klc -2) and the kinesin motor subunit ( unc-116 ) expressing an ida-1::gfp transgene that labels DCVs in the ALA neuron. A reduced-function unc-116(rf) mutation greatly impaired DCV transport in both directions. A klc-2(rf) reduced-function mutation decreased DCV velocity in both directions and reduced the frequency of body bends during swimming. In contrast, the klc-1(-) null mutation had no effect on anterograde transport or swimming ability, but surprisingly it increased the speed of retrograde DCV transport. We also determined lifespan, finding that klc-1(-) or klc-2(rf) single mutants were wild-type whereas the unc-116(rf) , ida-1::gfp and unc-116(rf) ; ida-1::gfp strains were short-lived. Strikingly, the ida-1::gfp transgenic synergistically interact with either klc mutant to extend lifespan compared to wild-type and parental strains. Our findings suggest that kinesin-1 not only influences anterograde and retrograde DCV transport but also plays a role in regulating lifespan.
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Gavrilova et al. (2024) studied this question.
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