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Cell Metab. 2015 Oct 6;22(4):734-740. doi: 10.1016/j.cmet.2015.08.001. Epub 2015 Aug 13.

Detection and Quantitation of Circulating Human Irisin by Tandem Mass Spectrometry.

Author information

1
Dana-Farber Cancer Institute and Department of Cell Biology, Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA.
2
Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue Boston, MA 02115.
3
Division of Endocrinology, 200 First Street SW, Joseph 5-193, Mayo Clinic, Rochester, MN 55905.
#
Contributed equally

Abstract

Exercise provides many health benefits, including improved metabolism, cardiovascular health, and cognition. We have shown previously that FNDC5, a type I transmembrane protein, and its circulating form, irisin, convey some of these benefits in mice. However, recent reports questioned the existence of circulating human irisin both because human FNDC5 has a non-canonical ATA translation start and because of claims that many human irisin antibodies used in commercial ELISA kits lack required specificity. In this paper we have identified and quantitated human irisin in plasma using mass spectrometry with control peptides enriched with heavy stable isotopes as internal standards. This precise state-of-the-art method shows that human irisin is mainly translated from its non-canonical start codon and circulates at ∼ 3.6 ng/ml in sedentary individuals; this level is increased to ∼ 4.3 ng/ml in individuals undergoing aerobic interval training. These data unequivocally demonstrate that human irisin exists, circulates, and is regulated by exercise.

PMID:
26278051
PMCID:
PMC4802359
DOI:
10.1016/j.cmet.2015.08.001
[Indexed for MEDLINE]
Free PMC Article

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