The filamin-B–refilin axis – spatiotemporal regulators of the actin-cytoskeleton in development and disease

Author:

Baudier Jacques12ORCID,Jenkins Zandra A.3,Robertson Stephen P.3

Affiliation:

1. Aix Marseille Université, CNRS, IBDM, 13284 Marseille Cedex 07, France

2. Institut de Biologie du Développement de Marseille-UMR CNRS 7288, Campus de Luminy-Case 907, 13288 Marseille Cedex 9, France

3. Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand

Abstract

ABSTRACT During development, cycles of spatiotemporal remodeling of higher-order networks of actin filaments contribute to control cell fate specification and differentiation. Programs for controlling these dynamics are hard-wired into actin-regulatory proteins. The filamin family of actin-binding proteins exert crucial mechanotransduction and signaling functions in tissue morphogenesis. Filamin-B (FLNB) is a key player in chondrocyte progenitor differentiation for endochondral ossification. Biallelic loss-of-function mutations or gain-of-function mutations in FLNB cause two groups of skeletal disorders that can be attributed to either the loss of repressive function on TGF-β signaling or a disruption in mechanosensory properties, respectively. In this Review, we highlight a unique family of vertebrate-specific short-lived filamin-binding proteins, the refilins (refilin-A and refilin-B), that modulate filamin-dependent actin crosslinking properties. Refilins are downstream TGF-β effectors in epithelial cells. Double knockout of both refilin-A and refilin-B in mice results in precocious ossification of some axial skeletal elements, leading to malformations that are similar to those seen in FLNB-deficient mice. Based on these findings, we present a model summarizing the role of refilins in regulating the mechanosensory functions of FLNB during skeletal development. We also discuss the possible contribution of refilins to FLNB-related skeletal pathologies that are associated with gain-of-function mutations.

Publisher

The Company of Biologists

Subject

Cell Biology

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