RESUMO
ß2 integrins are leukocyte-specific adhesion molecules that are essential for leukocyte recruitment. The lack of tools for reporting ß2 integrin activation in mice hindered the study of ß2 integrin-related immune responses in vivo. Here, we generated a humanized ß2 integrin knockin mouse strain by targeting the human ß2 integrin coding sequence into the mouse Itgb2 locus to enable imaging of ß2 integrin activation using the KIM127 (extension) and mAb24 (high-affinity) reporter antibodies. Using a CXCL1-induced acute inflammation model, we show the local dynamics of ß2 integrin activation in arresting neutrophils in vivo in venules of the mouse cremaster muscle. Activated integrins are highly concentrated in a small area at the rear of arresting neutrophils in vivo. In a high-dose lipopolysaccharide model, we find that ß2 integrins are activated in association with elevated neutrophil adhesion in lung and liver. Thus, these mice enable studies of ß2 integrin activation in vivo.
