AGE2010Full TextOpen Access

Plasma biomarkers of mouse aging

Juan Ding, John J. Kopchick

41 citations2010Open Access — see publisher for license terms1 related compound

Research Article — Peer-Reviewed Source

Original research published by Ding et al. in AGE. Redistributed under Open Access — see publisher for license terms. MedTech Research Group provides these references for informational purposes. We do not conduct original research. All studies are the work of their respective authors and institutions.

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Abstract

Normal aging is accompanied by a series of physiological changes such as gray hair, cataracts, reduced immunity, and increased susceptibility to disease. To identify novel biomarkers of normal aging, we analyzed plasma proteins of male mice longitudinally from 2 to 19 months of age. Plasma proteins were analyzed by two-dimensional gel electrophoresis and identified using mass spectrometry (MS), MS/MS and liquid chromatography MS/MS. We found that many plasma proteins exist as multiple isoforms with different masses and/or charges. Thirty-nine protein spots (corresponding to six distinct proteins) have been identified, 13 of which exhibited significant changes with age. For example, several proteins increased significantly during aging including one isoform of transthyretin, two isoforms of haptoglobin, and three isoforms of immunoglobulin kappa chain. Conversely, several proteins decreased significantly during aging including peroxiredoxin-2, serum amyloid protein A-1, and five isoforms of albumin. Identification of these proteins provides new biomarkers of normal aging in mice. If validated in humans, these biomarkers may facilitate therapeutic interventions to identify premature aging, delay aging, and/or improve healthspan of the elderly. Electronic supplementary material The online version of this article (doi:10.1007/s11357-010-9179-z) contains supplementary material, which is available to authorized users.

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Electronic supplementary material

The online version of this article (doi:10.1007/s11357-010-9179-z) contains supplementary material, which is available to authorized users.

Article Details
DOI10.1007/s11357-010-9179-z
PubMed ID20842533
PMC IDPMC3168609
JournalAGE
Year2010
AuthorsJuan Ding, John J. Kopchick
LicenseOpen Access — see publisher for license terms
Citations41