Abstract
Here we report the functional importance of profilin in various actin-mediated morphological changes using H119E mutant profilin I, which is deficient only in actin binding. In the case of actin-protrusive structures from the plasma membrane, H119E-profilin was shown to suppress the formation of Cdc42-induced actin microspikes and Rac-induced membrane ruffles. Conversely, Rho-induced stress fiber formation seemed to occur independently of H119E-profilin introduction. Furthermore, H119E-profilin blocked cleavage furrow ingression and subsequent adhesion to the substratum during cell division, a process in which actin plays indispensable roles.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3T3 Cells / cytology*
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3T3 Cells / drug effects
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3T3 Cells / metabolism
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Actins / metabolism
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Actins / ultrastructure*
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Animals
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Cell Cycle / physiology
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Cell Cycle Proteins / genetics
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Cell Cycle Proteins / metabolism
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Cell Division / physiology
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Cell Membrane / metabolism
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Cell Membrane / ultrastructure*
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Contractile Proteins*
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GTP-Binding Proteins / genetics
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GTP-Binding Proteins / metabolism
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HeLa Cells / cytology*
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HeLa Cells / metabolism
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Humans
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Lysophospholipids / pharmacology
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Mice
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Microfilament Proteins / metabolism*
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Microfilament Proteins / physiology*
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Mutation
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Platelet-Derived Growth Factor / pharmacology
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Profilins
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Recombinant Proteins / genetics
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Recombinant Proteins / metabolism
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cdc42 GTP-Binding Protein
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rac GTP-Binding Proteins
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rho GTP-Binding Proteins
Substances
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Actins
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Cell Cycle Proteins
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Contractile Proteins
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Lysophospholipids
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Microfilament Proteins
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PFN1 protein, human
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Pfn1 protein, mouse
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Platelet-Derived Growth Factor
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Profilins
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Recombinant Proteins
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GTP-Binding Proteins
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cdc42 GTP-Binding Protein
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rac GTP-Binding Proteins
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rho GTP-Binding Proteins