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Blood, 15 August 2007, Vol. 110, No. 4, pp. 1191-1198.
Prepublished online as a Blood First Edition Paper on May 8, 2007; DOI 10.1182/blood-2006-11-060103.


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IMMUNOBIOLOGY

Leukocyte PI3K{gamma} and PI3K{delta} have temporally distinct roles for leukocyte recruitment in vivo

Lixin Liu1, Kamal D. Puri2, Josef M. Penninger3, and Paul Kubes1

1 Immunology Research Group, Department of Physiology and Biophysics, University of Calgary, Calgary, Alberta, Canada; 2 Calistoga Pharmaceuticals, Seattle, WA; and 3 Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Vienna, Austria

Phosphoinositide 3-kinases (PI3Ks) have been considered important in leukocyte motility. PI3K{gamma}, the class IB PI3K, expressed prominently in leukocytes and also in endothelial cells, mediates leukocyte functional responses induced by chemoattractants. To reveal its role in leukocyte recruitment, we used intravital microscopy to directly visualize leukocyte rolling, adhesion, and emigration in postcapillary venules in PI3K{gamma}-deficient (PI3K{gamma}-/-) mice. We report here that PI3K{gamma} deficiency had no significant effects on leukocyte rolling flux or rolling velocity and minor effects on adhesion (30% to 35%) in response to CXC chemokine MIP-2 (CXCL2) or KC (CXCL1). However, leukocyte emigration was severely impaired in PI3K{gamma}-/- mice in an early (first 90 minutes) response to MIP-2 or KC. Chimeric mice receiving bone marrow transplants revealed that this early response was entirely dependent upon PI3K{gamma} in neutrophils but not parenchymal cells (endothelium and others). Identical responses were observed when endogenous chemokine production was induced by TNF{alpha}; leukocyte emigration was reduced in PI3K{gamma}-/- mice. More prolonged responses to MIP-2 (for 4 to 5 hours) or TNF{alpha} (6 to 8 hours) were almost entirely PI3K{gamma} independent and largely dependent on PI3K{delta}. Our results reveal that leukocyte emigration response to CXC chemokines is entirely dependent upon PI3K{gamma} or PI3K{delta}, but these are nonoverlapping, temporally distinct events in inflamed tissues in vivo.


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