Inactivation of CD11b in a mouse transgenic model protects against sepsis-induced lung PMN infiltration and vascular injury
| Autor: | Qinghui Liu, Dan Predescu, Michael Broman, Randall S. Frey, Xiao Pei Gao, Asrar B. Malik |
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| Rok vydání: | 2005 |
| Předmět: |
Neutrophils
Physiology Transgene Mice Transgenic Vascular permeability CD11a Lung injury Capillary Permeability Mice In vivo Sepsis Gram-Negative Bacteria Cell Adhesion Genetics Animals Edema Cell adhesion Lung Microvessel Escherichia coli Infections Glycoproteins CD11b Antigen Microscopy Confocal biology Endothelial Cells Membrane Proteins Helminth Proteins biochemical phenomena metabolism and nutrition Oxidants Molecular biology Neutrophil Infiltration Integrin alpha M Immunology biology.protein Protein Binding |
| Zdroj: | Physiological Genomics. 21:230-242 |
| ISSN: | 1531-2267 1094-8341 |
| DOI: | 10.1152/physiolgenomics.00291.2004 |
| Popis: | To inactivate chronically the β2-integrin CD11b (Mac-1), we made a transgenic model in mice in which we expressed the CD11b antagonist polypeptide neutrophil inhibitory factor (NIF). Using these mice, we determined the in vivo effects of CD11b inactivation on polymorphonuclear leukocyte (PMN) function and acute lung injury (ALI) induced by Escherichia coli septicemia. In wild-type PMNs, CD11b expression was induced within 1 h after E. coli challenge, whereas this response was significantly reduced in NIF+/+PMNs. Coimmunoprecipitation studies showed that NIF associated with CD11b in NIF+/+PMNs. To validate the effectiveness of CD11b blockade, we compared PMN function in NIF+/+and Mac-1-deficient (Mac-1−/−) mice. Adhesion of both Mac-1−/−and NIF+/+PMNs to endothelial cells in response to LPS was reduced in both types of PMNs and fully blocked only by the addition of anti-CD11a monoclonal antibody. This finding is indicative of intact CD11a function in the NIF+/+PMNs but the blockade of CD11b function. CD11b inactivation in NIF+/+mice interfered with lung PMN infiltration induced by E. coli and prevented the increase in lung microvessel permeability and edema formation, with most of the protection seen in the 1-h period after the E. coli. Thus our results demonstrate that CD11b plays a crucial role in mediating lung PMN sequestration and vascular injury in the early phase of gram-negative septicemia. The NIF+/+mouse model, in which CD11b is inactivated by binding to NIF, is a potentially useful model for in vivo assessment of the role of PMN CD11b in the mechanism of vascular inflammation. |
| Databáze: | OpenAIRE |
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