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Blood, 1 December 2006, Vol. 108, No. 12, pp. 3633-3634.
A new Rac-ket in red cellsTHE SCRIPPS RESEARCH INSTITUTE
A paper by Kalfa and colleagues in this issue of Blood shows that Rac GTPases regulate actin assembly in mouse red cells, overturning previous assumptions that actin filaments are stable structural elements in the spectrin-actin membrane skeleton.
This presumed stability of the actin in the red cell contrasts with the regulated and dynamic actin assembly and disassembly in other cell types, where the transmittance of extracellular signals to the actin cytoskeleton is accomplished through the Rho family proteins, Rac, Rho, and Cdc42.3 The function of these proteins is to serve as molecular switches, which activate a variety of actin regulators, including Arp2/3, formins, and cofilins. The mechanisms by which the Rho proteins activate these downstream targets are manifold, and include signaling through WASP, p21-activated kinase (PAK), Rho kinases (RhoK), protein kinase Cs (PKCs), and IQGAP. The ultimate result of this plethora of signals is constant: in all cases of Rho-family activation, actin dynamics is increased.
To study Rac signaling in red cells, Kalfa and colleagues have analyzed a hematopoietic-specific conditional knock-out for Rac1 in a Rac2-null genetic background. Mice whose red cells lack Rac1 and Rac2 develop a microcytic hemolytic anemia with bizarrely shaped microspherocytes, fragmented cells, and increased reticulocytosis. Rac1/2 knock-out red cells are less deformable, and their membrane skeletons are grossly disorganized, with gaps and aggregates in the actin filament network (see figure), increased levels of actin, and reduced levels of spectrin on the membrane. Notably, a striking increase in phosphorylation of adducin is observed at Ser724, a PKC site in the C-terminal actin-capping domain, and the phospho-adducin is released from the membrane skeleton of Rac1/2 knock-out red cells. In vitro, phosphorylation of adducin reduces its barbed-end capping activity and its ability to recruit spectrin to actin filaments.4 Thus, in the absence of Rac activity we can speculate that PKC phosphorylation of adducin and its dissociation from the membrane skeleton leads to uncapping of barbed ends and promotion of actin assembly, followed by filament rearrangements and destabilization of the spectrin-actin membrane skeleton.
The roles for actin filament assembly and turnover in the other cellular processes in which the rho family proteins are involved, such as cell migration, vesicular transport, and cell polarization are obvious.3 What actin dynamics would accomplish in the red cell is less clear. One possibility raised by the data from Kalfa and colleagues is that Rac signals and their accompanying actin dynamics are required during red cell maturation to correctly assemble the mature membrane skeleton. Alternatively, regulated turnover of the short actin filaments may help confer the remarkable deformability and dynamic plasticity of red cell shapes under shear stress in the circulation. In any case, it is clear that the red cell still has many lessons to teach us about actin dynamics and its regulation. Furthermore, this study points to likely roles of Rho-family proteins in the molecular mechanisms underlying abnormal red cell shape and deformability, and highlights these and other signaling proteins as potential new targets in treatment of hemolytic anemias.
The authors declare no competing financial interests. References
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| Copyright © 2006 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||||
