Cofilactin filaments regulate filopodial structure and dynamics in neuronal growth cones. 2022

Ryan K Hylton, and Jessica E Heebner, and Michael A Grillo, and Matthew T Swulius
Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA, USA.

Cofilin is best known for its ability to sever actin filaments and facilitate cytoskeletal recycling inside of cells, but at higher concentrations in vitro, cofilin stabilizes a more flexible, hyper-twisted state of actin known as "cofilactin". While this filament state is well studied, a structural role for cofilactin in dynamic cellular processes has not been observed. With a combination of cryo-electron tomography and fluorescence imaging in neuronal growth cones, we observe that filopodial actin filaments switch between a fascin-linked and a cofilin-decorated state, and that cofilactin is associated with a variety of dynamic events within filopodia. The switch to cofilactin filaments occurs in a graded fashion and correlates with a decline in fascin cross-linking within the filopodia, which is associated with curvature in the bundle. Our tomographic data reveal that the hyper-twisting of actin from cofilin binding leads to a rearrangement of filament packing, which largely excludes fascin from the base of filopodia. Our results provide mechanistic insight into the fundamentals of cytoskeletal remodeling inside of confined cellular spaces, and how the interplay between fascin and cofilin regulates the dynamics of searching filopodia.

UI MeSH Term Description Entries
D008841 Actin Cytoskeleton Fibers composed of MICROFILAMENT PROTEINS, which are predominately ACTIN. They are the smallest of the cytoskeletal filaments. Actin Filaments,Microfilaments,Actin Microfilaments,Actin Cytoskeletons,Actin Filament,Actin Microfilament,Cytoskeleton, Actin,Cytoskeletons, Actin,Filament, Actin,Filaments, Actin,Microfilament,Microfilament, Actin,Microfilaments, Actin
D011554 Pseudopodia A dynamic actin-rich extension of the surface of an animal cell used for locomotion or prehension of food. Axopodia,Filopodia,Lamellipodia,Lobopodia,Microspikes, Cell Surface,Reticulopodia,Pseudopodium,Cell Surface Microspike,Cell Surface Microspikes,Lamellipodias,Microspike, Cell Surface,Surface Microspike, Cell,Surface Microspikes, Cell
D000199 Actins Filamentous proteins that are the main constituent of the thin filaments of muscle fibers. The filaments (known also as filamentous or F-actin) can be dissociated into their globular subunits; each subunit is composed of a single polypeptide 375 amino acids long. This is known as globular or G-actin. In conjunction with MYOSINS, actin is responsible for the contraction and relaxation of muscle. F-Actin,G-Actin,Actin,Isoactin,N-Actin,alpha-Actin,alpha-Isoactin,beta-Actin,gamma-Actin,F Actin,G Actin,N Actin,alpha Actin,alpha Isoactin,beta Actin,gamma Actin
D051339 Actin Depolymerizing Factors A family of low MOLECULAR WEIGHT actin-binding proteins found throughout eukaryotes. They remodel the actin CYTOSKELETON by severing ACTIN FILAMENTS and increasing the rate of monomer dissociation. Actin Depolymerizing Protein,Cofilin,Cofilins,ADF Proteins (Actin Depolymerizing Factors),Actin Depolymerizing Proteins,Cofilin Proteins,Depolymerizing Factors, Actin,Depolymerizing Protein, Actin,Depolymerizing Proteins, Actin,Protein, Actin Depolymerizing
D020439 Growth Cones Bulbous enlargement of the growing tip of nerve axons and dendrites. They are crucial to neuronal development because of their pathfinding ability and their role in synaptogenesis. Growth Cone

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