Increased neutrophil respiratory burst in bcr-null mutants.

Journal:

Cell 1995 Mar

Authors:

Voncken JW, van Schaick H, Kaartinen V, Deemer K, Coates T, Landing B, Pattengale P, Dorseuil O, Bokoch GM, Groffen J

Abstract

Philadelphia (Ph)-positive leukemias invariably contain a chromosomal translocation fusing BCR to ABL. The BCR-ABL protein is responsible for leukemogenesis. Here we show that exposure of bcr-null mutant mice to gram-negative endotoxin led to severe septic shock and increased tissue injury by neutrophils. Neutrophils of bcr (-/-) mice showed a pronounced increase in reactive oxygen metabolite production upon activation and were more sensitive to priming stimuli. Activated (-/-) neutrophils displ
...[more]
ayed a 3-fold increased p21rac2 membrane translocation compared with (+/+) neutrophils. These results connect Bcr in vivo with the regulation of Rac-mediated superoxide production by the NADPH-oxidase system of leukocytes and suggest a link between Bcr function and the cell type affected in Ph-positive leukemia.[less]

Mesh Headings:

Actin Cytoskeleton, Animals, Endotoxins, Female, GTP-Binding Proteins, Gene Targeting, Lipopolysaccharides, Male, Mice, Mice, Inbred C57BL, Mutation, Neutropenia, Neutrophil Activation, Neutrophils, Oncogene Proteins, Protein-Tyrosine Kinases, Proto-Oncogene Proteins, Proto-Oncogene Proteins c-bcr, Respiratory Burst, Shock, Septic, Superoxides, Toxemia, rac GTP-Binding Proteins