SH4-domain-induced plasma membrane dynamization promotes bleb-associated cell motility

• DOI: 10.1242/jcs.011130
• Publication Date: 2007-10-24T06:44:39Z
• Authors: Stella Tournaviti; Sebastian Hannemann; Stefan Terjung; Thomas M. Kitzing; Carolin Stegmayer; Julia Ritzerfeld; Paul Walther; Robert Grosse; Walter Nickel; Oliver T. Fackler
• Keywords: Leishmania; rho GTP-Binding Proteins; 0301 basic medicine; Myosin Light Chains; Recombinant Fusion Proteins; Amino Acid Motifs; Cell Membrane; Protozoan Proteins; Antigens, Protozoan; CHO Cells; 03 medical and health sciences; Cricetulus; src-Family Kinases; Cell Movement; Cricetinae; Animals; Humans; Cell Surface Extensions; HeLa Cells

SH4 domains provide bipartite membrane-targeting signals for oncogenic Src family kinases. Here we report the induction of non-apoptotic plasma membrane (PM) blebbing as a novel and conserved activity of SH4 domains derived from the prototypic Src kinases Src, Fyn, Yes and Lck as well as the HASPB protein of Leishmania parasites. SH4-domain-induced blebbing is highly dynamic, with bleb formation and collapse displaying distinct kinetics. These reorganizations of the PM are controlled by Rho but not Rac or Cdc42 GTPase signalling pathways. SH4-induced membrane blebbing requires the membrane association of the SH4 domain, is regulated by the activities of Rock kinase and myosin II ATPase, and depends on the integrity of F-actin as well as microtubules. Endogenous Src kinase activity is crucial for PM blebbing in SH4-domain-expressing cells, active Src and Rock kinases are enriched in SH4-domain-induced PM blebs, and PM blebbing correlates with enhanced cell invasion in 3D matrices. These results establish a novel link between SH4 domains, Src activity and Rho signalling, and implicate SH4-domain-mediated PM dynamization as a mechanism that influences invasiveness of cells transformed by SH4-domain-containing oncoproteins.