Atsuko Uchida

Tight Functional Coupling of Kinesin-1A and Dynein Motors in the Bidirectional Transport of Neurofilaments

We have tested the hypothesis that kinesin-1A (formerly KIF5A) is an anterograde motor for axonal neurofilaments. In cultured sympathetic neurons from kinesin-1A knockout mice, we observed a 75% reduction in the frequency of both anterograde and retrograde neurofilament movement. This transport defect could be rescued by kinesin-1A, and with successively decreasing efficacy by kinesin-1B and kinesin-1C. In wild-type neurons, headless mutants of kinesin-1A and kinesin-1C inhibited both anterograde and retrograde movement in a dominant-negative manner. Because dynein is thought to be the retrograde motor for axonal neurofilaments, we investigated the effect of dynein inhibition on anterograde and retrograde neurofilament transport. Disruption of dynein function by using RNA interference, dominant-negative approaches, or a function-blocking antibody also inhibited both anterograde and retrograde neurofilament movement. These data suggest that kinesin-1A is the principal but not exclusive anterograde motor for neurofilaments in these neurons, that there may be some functional redundancy among the kinesin-1 isoforms with respect to neurofilament transport, and that the activities of the anterograde and retrograde neurofilament motors are tightly coordinated.

Magnetostriction and magnetic texture to 100.75 Tesla in frustrated SrCu2(BO3)2

Strong geometrical frustration in magnets leads to exotic states such as spin liquids, spin supersolids, and complex magnetic textures. SrCu2(BO3)2, a spin-1/2 Heisenberg antiferromagnet in the archetypical Shastry–Sutherland lattice, exhibits a rich spectrum of magnetization plateaus and stripe-like magnetic textures in applied fields. The structure of these plateaus is still highly controversial due to the intrinsic complexity associated with frustration and competing length scales. We discover magnetic textures in SrCu2(BO3)2 via magnetostriction and magnetocaloric measurements in fields up to 100.75 T. In addition to observing low-field fine structure with unprecedented resolution, the data also reveal lattice responses at 73.6 T and at 82 T that we attribute, using a controlled density matrix renormalization group approach, to a unanticipated 2/5 plateau and to the long-predicted 1/2 plateau.

Severing and end-to-end annealing of neurofilaments in neurons

Significance Neurofilaments, which are the intermediate filaments of neurons, are major components of nerve cells, but their assembly dynamics have not been determined. Here we demonstrate efficient end-to-end annealing of neurofilaments in nerve cells, and we show that there also is a mechanism that severs these polymers. Our efforts thus identify severing of neuronal intermediate filaments in vivo and suggest a mechanism for regulating intermediate filament length involving a dynamic cycle of severing and end-to-end annealing. We have shown previously that neurofilaments and vimentin filaments expressed in nonneuronal cell lines can lengthen by joining ends in a process known as “end-to-end annealing.” To test if this also occurs for neurofilaments in neurons, we transfected cultured rat cortical neurons with fluorescent neurofilament fusion proteins and then used photoconversion or photoactivation strategies to create distinct populations of red and green fluorescent filaments. Within several hours we observed the appearance of chimeric filaments consisting of alternating red and green segments, which is indicative of end-to-end annealing of red and green filaments. However, the appearance of these chimeric filaments was accompanied by a gradual fragmentation of the red and green filament segments, which is indicative of severing. Over time we observed a progressive increase in the number of red–green junctions along the filaments accompanied by a progressive decrease in the average length of the alternating red and green fluorescent segments that comprised those filaments, suggesting a dynamic cycle of severing and end-to-end-annealing. Time-lapse imaging of the axonal transport of chimeric filaments demonstrated that the red and green segments moved together, confirming that they were indeed part of the same filament. Moreover, in several instances, we also were able to capture annealing and severing events live in time-lapse movies. We propose that the length of intermediate filaments in cells is regulated by the opposing actions of severing and end-to-end annealing, and we speculate that this regulatory mechanism may influence neurofilament transport within axons.

Live-cell imaging of neurofilament transport in cultured neurons.

Neurofilaments, which are the intermediate filaments of nerve cells, are space-filling cytoskeletal polymers that contribute to the growth of axonal caliber. In addition to their structural role, neurofilaments are cargos of axonal transport that move along microtubule tracks in a rapid, intermittent, and bidirectional manner. Though they measure just 10nm in diameter, which is well below the diffraction limit of optical microscopes, these polymers can reach 100 μm or more in length and are often packed densely, just tens of nanometers apart. These properties of neurofilaments present unique challenges for studies on their movement. In this article, we describe several live-cell fluorescence imaging strategies that we have developed to image neurofilament transport in axons of cultured neurons on short and long timescales. Together, these methods form a powerful set of complementary tools with which to study the axonal transport of these unique intracellular cargos.

Influence of a GSK3β phosphorylation site within the proximal C-terminus of Neurofilament-H on neurofilament dynamics

ABSTRACT Phosphorylation of the C-terminal tail of the heavy neurofilament subunit (NF-H) impacts neurofilament (NF) axonal transport and residence within axons by fostering NF-NF associations that compete with transport. We tested the role of phosphorylation of a GSK-3β consensus site (S493) located in the proximal portion of the NF-H tail in NF dynamics by transfection of NB2a/d1 cells with NF-H, where S493 was mutated to aspartic acid (S493D) or to alanine (S493A) to mimic constitutive phosphorylation and non-phosphorylation. S493D underwent increased transport into axonal neurites, while S493A displayed increased perikaryal NF aggregates that were decorated by anti-kinesin. Increased levels of S493A co-precipitated with anti-kinesin indicating that reduced transport of S493A was not due to reduced kinesin association but due to premature NF-NF interactions within perikarya. S493D displayed increased phospho-immunoreactivity within axonal neurites at downstream C-terminal sites attributable to mitogen-activated protein kinase and cyclin-dependent kinase 5. However, S493D was more prone to proteolysis following kinase inhibition, suggesting that S493 phosphorylation is an early event that alters sidearm configuration in a manner that promotes appropriate NF distribution. We propose a novel model for sidearm configuration. Summary: We demonstrate that phosphorylation of a critical site regulates neurofilament transport, proteolysis and interaction with other axonal cytoskeletal elements, and present evidence that it does so by altering protein conformation. This article has an associated First Person interview with the first author of the paper as part of the supplementary information.

Neurofilaments in Aged Animals

Neurofilaments (NFs) are neuronal intermediate filaments assembled mainly from three subunit proteins, NF-L, NF-M and NF-H. NFs are the major cytoskeletal element of axons, particularly large myelinated axons. Accumulation of NFs in the cell body or proximal axons is a hallmark of motor neuron diseases, of which aging is a risk factor. It is not known whether the accumulation of NFs is the primary causative factor of these diseases; however, it is feasible that accumulated NFs are obstacles for axonal trafficking, resulting in a decreased supply of proteins and organelles required for the maintenance of or activity in the distal axons. Axonal transport of NFs slows down with aging and the decreased rate of transport could be a risk factor for disease. Therefore, it is important to determine age-dependent changes in properties of NFs. In this chapter we review the characteristics of NFs in aged animals. The most striking morphological change in NFs is their density within axons. NFs are more than twice as densely packed in the proximal region of aged rat sciatic nerve axons compared with those in young adult rats. A remarkable biochemical change is the reduction of NF-M content in aged NFs. This is partly because of the reduced transcription of NF-M in aged rats. The relationship between NF packing and reduced NF-M is discussed in terms of the age-dependent decrease in axonal transport and neurodegenerative diseases.