4.8 Article

Gαi2-mediated signaling events in the endotheliurn are involved in controlling leukocyte extravasation

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0700185104

Keywords

G proteins; inflammation; knockout mice; leukocyte trafficking; pulmonary models

Funding

  1. NCRR NIH HHS [K26 RR 019709, K26 RR019709] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL058723, R01 HL069428, R01 HL068171, R01 HL065228, HL 68171, HL 065228, R01 HL079304, HL 079304, R56 HL058723, HL 058723] Funding Source: Medline
  3. NIAID NIH HHS [R29 AI035796, AI 35796, R01 AI035796] Funding Source: Medline
  4. NIDDK NIH HHS [DK 19318] Funding Source: Medline
  5. NIGMS NIH HHS [R37 GM034236, GM 34236] Funding Source: Medline

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The trafficking of leukocytes from the blood to sites of inflammation is the cumulative result of receptor-ligand-mediated signaling events associated with the leukocytes themselves as well as with the underlying vascular endothelium. Our data show that Gal signaling pathways in the vascular endothelium regulate a critical step required for leukocyte diapedesis. In vivo studies using knockout mice demonstrated that a signaling event in a non-lymphohematopoietic compartment of the lung prevented the recruitment of proinflammatory leukocytes. Intravital microscopy showed that blockade was at the capillary endothelial surface and ex vivo studies of leukocyte trafficking demonstrated that a G alpha(i)-signaling event in endothelial cells was required for transmigration. Collectively, these data suggest that specific G alpha(i2)-mediated signaling between endothelial cells and leukocytes is required for the extravasation of leukocytes and for tissue-specific accumulation.

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