Key result
Expression of the FLNB-W148R mutation induced prominent F-actin accumulations, cytoskeletal rearrangement, and delayed directional cell migration.
The pathological W148R mutation in filamin B induces F-actin clustering and limits cytoskeletal reorganization, providing a potential cellular mechanism for associated skeletal developmental abnormalities.
FLNB ABD mutations disrupt actin reorganization in vitro; hypothesis-generating for skeletal dysplasia mechanisms, prospective studies needed before clinical relevance.
Filamin B (FLNB) is a dimeric actin-binding protein that orchestrates the reorganization of the actin cytoskeleton. Congenital mutations of FLNB at the actin-binding domain (ABD) are known to cause abnormalities of skeletal development, such as atelosteogenesis types I and III and Larsen's syndrome, although the underlying mechanisms are poorly understood. Here, using fluorescence microscopy, we characterized the reorganization of the actin cytoskeleton in cells expressing each of six pathological FLNB mutants that have been linked to skeletal abnormalities. The subfractionation assay showed a greater accumulation of the FLNB ABD mutants W148R and E227K than the wild-type protein to the cytoskeleton. Ectopic expression of FLNB-W148R and, to a lesser extent, FLNB-E227K induced prominent F-actin accumulations and the consequent rearrangement of focal adhesions, myosin II, and septin filaments and results in a delayed directional migration of the cells. The W148R protein-induced cytoskeletal rearrangement was partially attenuated by the inhibition of myosin II, p21-activated protein kinase, or Rho-associated protein kinase. The expression of a single-head ABD fragment with the mutations partially mimicked the rearrangement induced by the dimer. The F-actin clustering through the interaction with the mutant FLNB ABD may limit the cytoskeletal reorganization, preventing normal skeletal development.
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Zhao et al. (2015) studied Skeletal abnormalities (atelosteogenesis types I and III and Larsen's syndrome). Pathological FLNB mutants (W148R and E227K) vs. Wild-type FLNB protein was evaluated on Reorganization of the actin cytoskeleton and cell migration. Expression of the FLNB-W148R mutation induced prominent F-actin accumulations, cytoskeletal rearrangement, and delayed directional cell migration.
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