Research Paper Volume 12, Issue 4 pp 3502—3515
Successful aging: insights from proteome analyses of healthy centenarians
- 1 Research Institute of the Hospital 12 de Octubre ("imas12"), Madrid, Spain
- 2 i+HeALTH, European University Miguel de Cervantes, Valladolid, Spain
- 3 Systems Biology Department, University of Alcalá, Madrid, Spain
- 4 Achucarro Basque Center for Neuroscience, Science Park of the UPV/EHU, Leioa, Spain
- 5 Sorbonne University, GRC no. 21, Alzheimer Precision Medicine (APM), Pitié-Salpêtrière Hospital, Paris, France
- 6 Brain and Spine Institute (ICM), Paris, France
- 7 Institute of Memory and Alzheimer's Disease, Department of Neurology, Pitié-Salpêtrière Hospital, Paris, France
- 8 Centre for Primary Health Care Research, Lund University/Region Skane, Skane University Hospital, Malmo, Sweden
- 9 Nutriscience – Education and Consulting, Lisbon, Portugal
- 10 Faculty of Sport Sciences, European University of Madrid, Madrid, Spain
- 11 Laboratory of Cardiovascular Proteomics, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain
- 12 Centro Integrado de Investigación Biomédica en Red en Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain
- 13 2E Science, Robbio, Italy
- 14 Department of Genetics, Physical Anthropology and Animal Physiology, Faculty of Science and Technology, UPV/EHU, Leioa, Spain
- 15 IKERBASQUE, Basque Foundation for Science, Bilbao, Spain
- 16 Centro de Investigación Biomédica en Red, Fragilidad y Envejecimiento Saludable (CIBERFES), Madrid, Spain
Received: November 27, 2019 Accepted: January 28, 2020 Published: February 25, 2020
https://doi.org/10.18632/aging.102826How to Cite
Copyright © 2020 Santos-Lozano et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Healthy aging depends on a complex gene-environment network that is ultimately reflected in the expression of different proteins. We aimed to perform a comparative analysis of the plasma proteome of healthy centenarians (n=9, 5 women, age range 100–103 years) with a notably preserved ambulatory capacity (as a paradigm of ‘successful’ aging), and control individuals who died from a major age-related disease before the expected life expectancy (n=9, 5 women, age range: 67–81 years), and while having impaired ambulatory capacity (as a paradigm of ‘unsuccessful’ aging). We found that the expression of 49 proteins and 86 pathways differed between the two groups. Overall, healthy centenarians presented with distinct expression of proteins/pathways that reflect a healthy immune function, including a lower pro-inflammatory status (less ‘inflammaging’ and autoimmunity) and a preserved humoral immune response (increased B cell-mediated immune response). Compared with controls, healthy centenarians also presented with a higher expression of proteins involved in angiogenesis and related to enhanced intercellular junctions, as well as a lower expression of proteins involved in cardiovascular abnormalities. The identification of these proteins/pathways might provide new insights into the biological mechanisms underlying the paradigm of healthy aging.