Free IL-15 Is More Abundant Than IL-15 Complexed With Soluble IL-15 Receptor-α in Murine Serum: Implications for the Mechanism of IL-15 Secretion

Author:

Anderson Barbara G.12,Quinn LeBris S.132

Affiliation:

1. Geriatric Research, Education, and Clinical Center (B.G.A., L.S.Q.), Veteran's Administration Puget Sound Health Care System, Seattle, Washington 98108

2. Division of Gerontology and Geriatric Medicine (B.G.A., L.S.Q.), Department of Medicine, University of Washington, Seattle, Washington 98195

3. Research Service (L.S.Q.), Veteran's Administration Puget Sound Health Care System, Seattle, Washington 98108

Abstract

Abstract IL-15 is a cytokine that is part of the innate immune system, as well as a proposed myokine released from skeletal muscle during physical exercise that mediates many of the positive physiological effects of exercise. Many of the immune functions of IL-15 are mediated by juxtacrine signaling via externalized IL-15 bound to membrane-associated IL-15 receptor-α (IL-15Rα). Serum and plasma samples also contain measurable concentrations of IL-15, believed to arise from proteolytic cleavage of membrane-associated IL-15/IL-15Rα complexes to generate soluble IL-15/IL-15Rα species. Here, we validate commercial assays that can distinguish the free form of IL-15 and IL-15/IL-15Rα complexes. These assays showed that most (86%) IL-15 in mouse serum resides in the free state, with a minor proportion (14%) residing in complex with IL-15Rα. Given the much shorter half-life of free IL-15 compared with IL-15/IL-15Rα complexes, these findings cast doubt on the currently accepted model for IL-15 secretion from cleavage of membrane-bound IL-15/IL-15Rα and suggest that IL-15 is released as a free molecule by an unknown mechanism.

Publisher

The Endocrine Society

Subject

Endocrinology

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