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The protein kindlin 3 is mutated in the leukocyte adhesion deficiency III (LAD-III) disorder, leading to widespread infection due to the failure of leukocytes to migrate into infected tissue sites. To gain understanding of how kindlin 3 controls leukocyte function, we have focused on its pleckstrin homology (PH) domain and find that deletion of this domain eliminates the ability of kindlin 3 to participate in adhesion and migration of B cells mediated by the leukocyte integrin lymphocyte function-associated antigen 1 (LFA-1). PH domains are often involved in membrane localization of proteins through binding to phosphoinositides. We show that the kindlin 3 PH domain has binding affinity for phosphoinositide PI(3,4,5)P 3 over PI(4,5)P 2 . It has a major role in membrane association of kindlin 3 that is enhanced by the binding of LFA-1 to intercellular adhesion molecule 1 (ICAM-1). A splice variant, kindlin 3-IPRR, has a four-residue insert in the PH domain at a critical site that influences phosphoinositide binding by enhancing binding to PI(4,5)P 2 as well as by binding to PI(3,4,5)P 3 . However kindlin 3-IPRR is unable to restore the ability of LAD-III B cells to adhere to and migrate on LFA-1 ligand ICAM-1, potentially by altering the dynamics or PI specificity of binding to the membrane. Thus, the correct functioning of the kindlin 3 PH domain is central to the role that kindlin 3 performs in guiding lymphocyte adhesion and motility behavior, which in turn is required for a successful immune response. Background: Kindlin 3 is mutated in LAD-III causing widespread infection, but its role in leukocyte function is incompletely understood. Results: Deletion of the PH domain removes kindlin 3 from lymphocyte cell membrane and eliminates adhesion and migration. Conclusion: The PH domain is intrinsic to kindlin 3 regulation of integrin LFA-1-mediated lymphocyte function. Significance: A successful immune response depends on kindlin 3, and its PH subdomain is crucial.
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Hart et al. (2013) studied this question.
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