Preformed Membrane-Associated Stores of Interleukin (Il)-12 Are a Previously Unrecognized Source of Bioactive IL-12 That Is Mobilized within Minutes of Contact with an Intracellular Parasite

Author:

Quinones Marlon12,Ahuja Sunil K.12,Melby Peter C.12,Pate Lyle2,Reddick Robert L.3,Ahuja Seema S.12

Affiliation:

1. South Texas Veterans Health Care System, Audie L. Murphy Division, the

2. Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900

3. Department of Pathology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229-3900

Abstract

The prevailing paradigm is that production of the interleukin (IL)-12 p70 heterodimer, a critical T helper cell type 1 (Th1)–inducing cytokine, depends on the induced transcription of the p40 subunit. Concordant with this paradigm, we found that dendritic cells (DCs) produced IL-12 p70 only after at least 2–4 h of stimulation with lipopolysaccharide plus interferon γ. However, using several complementary experimental approaches, including electron and confocal microscopy, we now show that resting murine and human myeloid cells, including macrophages/DCs and DC-rich tissues, contain a novel source of bioactive IL-12 that is preformed and membrane associated. These preformed, membrane-associated IL-12 p70 stores are released within minutes after in vitro or in vivo contact with Leishmania donovani, an intracellular pathogen. Our findings highlight a novel source of bioactive IL-12 that is readily available for the rapid initiation of Th1 host responses to pathogens such as Leishmania species.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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