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Arf6:: a new player in FcγRIIIA lymphocyte-mediated cytotoxicity
被引:43
作者:
Galandrini, R
Micucci, F
Tassi, I
Cifone, MG
Cinque, B
Piccoli, M
Frati, L
Santoni, A
机构:
[1] Univ Roma La Sapienza, Dept Expt Med & Pathol, Ist Pasteur, Fdn Cenci Bolognetti, I-00161 Rome, Italy
[2] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
[3] Ist Mediterraneo Neurosci, Pozzilli, Italy
来源:
关键词:
D O I:
10.1182/blood-2004-10-4100
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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 phosphatidlylinositol4phosphate 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 phosphatidylinosito14,5-bisphosphate (PIP2) plasma membrane pool required for cytolytic granule-mediated target cell killing.
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页码:577 / 583
页数:7
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