Macrophage/microglia-specific protein Iba1 enhances membrane ruffling and Rac activation via phospholipase C-gamma -dependent pathway

J Biol Chem. 2002 May 31;277(22):20026-32. doi: 10.1074/jbc.M109218200. Epub 2002 Mar 26.

Abstract

Iba1 is a macrophage/microglia-specific calcium-binding protein that is involved in RacGTPase-dependent membrane ruffling and phagocytosis. In this study, we introduced Iba1 into Swiss 3T3 fibroblasts and demonstrated the enhancement of platelet-derived growth factor (PDGF)-induced membrane ruffling and chemotaxis. Wortmannin treatment did not completely suppressed this enhanced membrane ruffling in Iba1-expressing cells, whereas it did in Iba1-nonexpressing cells, suggesting that the enhancement is mediated through a phosphatidylinositol 3-kinase (PI3K)-independent signaling pathway. Porcine aorta endothelial cells transfected with expression constructs of Iba1 and PDGF receptor add-back mutants were used to analyze the signaling pathway responsible for the Iba1-induced enhancement of membrane ruffling. In the absence of Iba1 expression, PDGF did not induced membrane ruffling in cells expressing the Tyr-1021 receptor mutant, which is capable of activating phospholipase C-gamma (PLC-gamma) but not PI3K. In contrast, in the presence of Iba1 expression, membrane ruffling was formed in cells expressing the Tyr-1021 mutant. In addition, Rac was shown to be activated during membrane ruffling in cells expressing Iba1 and the Tyr-1021 mutant. Furthermore, dominant negative forms of PLC-gamma completely suppressed PDGF-induced Iba1-dependent membrane ruffling and Rac activation. These results indicate the existence of a novel signaling pathway where PLC-gamma activates Rac in a manner dependent on Iba1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Blotting, Western
  • CHO Cells
  • Calcium-Binding Proteins / metabolism*
  • Cell Membrane / metabolism*
  • Chemotaxis
  • Cricetinae
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Immunohistochemistry
  • Isoenzymes / metabolism*
  • Macrophages / metabolism*
  • Mice
  • Microfilament Proteins
  • Microglia / metabolism*
  • Microscopy, Fluorescence
  • Phalloidine / pharmacology
  • Phospholipase C gamma
  • Platelet-Derived Growth Factor / pharmacology
  • Precipitin Tests
  • Signal Transduction
  • Swine
  • Time Factors
  • Transfection
  • Type C Phospholipases / metabolism*
  • rac GTP-Binding Proteins / metabolism*

Substances

  • Aif1 protein, mouse
  • Calcium-Binding Proteins
  • Enzyme Inhibitors
  • Isoenzymes
  • Microfilament Proteins
  • Platelet-Derived Growth Factor
  • Phalloidine
  • Type C Phospholipases
  • Phospholipase C gamma
  • rac GTP-Binding Proteins