Centenarian hippocampus displays high levels of astrocytic metallothioneins

Author:

Saenz‐Antoñanzas Ander1,Muñoz‐Culla Maider234,Rigo Piero5,Ruiz‐Barreiro Leire6,Moreno‐Valladares Manuel1,Alberro Ainhoa23,Cruces‐Salguero Sara1,Arroyo‐Izaga Marta7,Arranz Amaia M.68,Otaegui David23ORCID,Guillemot François5,Matheu Ander189ORCID

Affiliation:

1. Cellular Oncology Group Biodonostia Health Research Institute San Sebastian Spain

2. Multiple Sclerosis Group Biodonostia Health Research Institute San Sebastian Spain

3. CIBERNED, ISCIII Madrid Spain

4. Department of Basic Psychological Processes and their Development University of the Basque Country (UPV/EHU) San Sebastian Spain

5. Neural Stem Cell Biology Laboratory The Francis Crick Institute London UK

6. Laboratory of Humanized Models of Disease, Achucarro Basque Center for Neuroscience Leioa Spain

7. BIOMICs Research Group, Microfluidics & BIOMICs, Department of Pharmacy and Food Sciences, Lascaray Research Center University of the Basque Country (UPV/EHU), Bioaraba Vitoria Spain

8. IKERBASQUE, Basque Foundation for Science Bilbao Spain

9. CIBERFES, ISCIII Madrid Spain

Abstract

AbstractThe hippocampus is a brain area linked to cognition. The mechanisms that maintain cognitive activity in humans are poorly understood. Centenarians display extreme longevity which is generally accompanied by better quality of life, lower cognitive impairment, and reduced incidence of pathologies including neurodegenerative diseases. We performed transcriptomic studies in hippocampus samples from individuals of different ages (centenarians [≥97 years], old, and young) and identified a differential gene expression pattern in centenarians compared to the other two groups. In particular, several isoforms of metallothioneins (MTs) were highly expressed in centenarians. Moreover, we identified that MTs were mainly expressed in astrocytes. Functional studies in human primary astrocytes revealed that MT1 and MT3 are necessary for their homeostasis maintenance. Overall, these results indicate that the expression of MTs specifically in astrocytes is a mechanism for protection during aging.

Funder

Diputación Foral de Gipuzkoa

Instituto de Salud Carlos III

Publisher

Wiley

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