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Blood, 15 July 2005, Vol. 106, No. 2, pp. 577-583.
Prepublished online as a Blood First Edition Paper on April 7, 2005; DOI 10.1182/blood-2004-10-4100.


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IMMUNOBIOLOGY

Arf6: a new player in Fc{gamma}RIIIA lymphocyte-mediated cytotoxicity

Ricciarda Galandrini, Federica Micucci, Ilaria Tassi, Maria Grazia Cifone, Benedetta Cinque, Mario Piccoli, Luigi Frati, and Angela Santoni

From the Department of Experimental Medicine and Pathology, Istituto Pasteur-Fondazione Cenci-Bolognetti, University "La Sapienza," Rome, Italy; the Department of Experimental Medicine, University of L'Aquila, Italy; and the Istituto Mediterraneo di Neuroscienze "Neuromed," Pozzilli, Italy.

The activation of phosphoinositide metabolism represents a critical step in the signaling pathways leading to the activation of cytolytic machinery, but its regulation is partially understood. We report here that the stimulation of the low-affinity receptor for immunoglobulin G (IgG) (Fc{gamma}RIIIA, CD16) on primary human natural killer (NK) cells induces a phosphatidylinositol 3-kinase (PI3K)–dependent activation of the small G protein Arf6. We first demonstrate a functional role for Arf6-dependent signals in the activation of the antibody-dependent cellular cytotoxicity (ADCC) attributable to the control of secretion of lytic granule content. We also show that Arf6 couples CD16 to the lipid-modifying enzymes phosphatidylinositol4phosphate 5-kinase type I alpha (PI5KI{alpha}) and phospholipase D (PLD) that are involved in the control of granule secretion; Arf6, but not Rho family small G proteins RhoA and Rac1, is required for receptor-induced PI5KI{alpha} membrane targeting as well as for PI5KI{alpha} and PLD activation. Our findings suggest that Arf6 plays a crucial role in the generation of a phosphatidylinositol4,5-bisphosphate (PIP2) plasma membrane pool required for cytolytic granule-mediated target cell killing.


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