Journal
JOURNAL OF IMMUNOLOGY
Volume 166, Issue 6, Pages 4115-4123Publisher
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.166.6.4115
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- NHLBI NIH HHS [HL54476] Funding Source: Medline
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There is mounting evidence that alpha (4) (CD49d) integrins are involved in neutrophil recruitment and function during inflammatory responses. We report that all resting murine neutrophils derived from bone marrow or peripheral blood express easily detectable levels of alpha (4) integrins on their surface. These alpha (4) integrins were functional, as demonstrated by stimulation of respiratory burst when neutrophils adhered to surfaces coated with the murine vascular cell adhesion molecule-1 (mVCAM-1). Adhesion occurred via alpha (4) integrins, as preincubation of neutrophils with an anti-alpha (4)-specific Ab inhibited attachment to mVCAM-1. Direct crosslinking of the alpha (4) integrin subunit by surface-bound mAbs also elicited superoxide release and release of the secondary granule marker, lactoferrin, The functional responses that occurred downstream of alpha (4) integrin cross-linking required signaling by Src family kinases, Neutrophils derived from hck(-/-)fgr(-/-)lyn(-/-) triple-knockout or hck(-/-)fgr(-/-) double-knockout mice failed to undergo respiratory burst when plated on mVCAM-1. Triple mutant neutrophils were also defective in release of both superoxide nd lactoferrin when plated on surfaces coated with mAbs directed against alpha (4). Correlated with impaired alpha (4)-induced functional responses, triple-mutant neutrophils also failed to spread and tightly adhere to anti-alpha (4) mAb-coated surfaces. This is the first direct evidence that functional alpha (4) integrins are expressed by murine PMNs, acid that these surface molecules can mediate cellular responses such as tight adhesion, spreading, sustained respiratory burst, and specific granule release in vitro, Moreover the alpha (4) integrins, like all other integrins tested, use the Src family kinases to transduce intracellular signals.
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