Hydrostatic pressure prevents chondrocyte differentiation through heterochromatin remodeling

Author:

Maki Koichiro1234,Nava Michele M.1235,Villeneuve Clémentine123,Chang Minki4,Furukawa Katsuko S.4,Ushida Takashi4,Wickström Sara A.12356ORCID

Affiliation:

1. Helsinki Institute of Life Science, Biomedicum, University of Helsinki, 00290 Helsinki, Finland

2. Wihuri Research Institute, Biomedicum, University of Helsinki, 00290 Helsinki, Finland

3. Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland

4. Department of Mechanical Engineering, The University of Tokyo, Tokyo 113-0033, Japan

5. Max Planck Institute for Biology of Ageing, 50931 Cologne, Germany

6. Cologne Excellence Cluster for Stress Responses in Ageing-associated diseases (CECAD), University of Cologne, 50931 Cologne, Germany

Abstract

ABSTRACT Articular cartilage protects and lubricates joints for smooth motion and transmission of loads. Owing to its high water content, chondrocytes within the cartilage are exposed to high levels of hydrostatic pressure, which has been shown to promote chondrocyte identity through unknown mechanisms. Here, we investigate the effects of hydrostatic pressure on chondrocyte state and behavior, and discover that application of hydrostatic pressure promotes chondrocyte quiescence and prevents maturation towards the hypertrophic state. Mechanistically, hydrostatic pressure reduces the amount of trimethylated H3K9 (K3K9me3)-marked constitutive heterochromatin and concomitantly increases H3K27me3-marked facultative heterochromatin. Reduced levels of H3K9me3 attenuates expression of pre-hypertrophic genes, replication and transcription, thereby reducing replicative stress. Conversely, promoting replicative stress by inhibition of topoisomerase II decreases Sox9 expression, suggesting that it enhances chondrocyte maturation. Our results reveal how hydrostatic pressure triggers chromatin remodeling to impact cell fate and function. This article has an associated First Person interview with the first author of the paper.

Funder

Helsinki Institute of Life Science

Wihuri Research Institute

Academy of Finland

Max Planck Society

Japan Society for the Promotion of Science

Nakatomi Foundation

Yamada Science Foundation

Marie Sklodowska-Curie Actions

Publisher

The Company of Biologists

Subject

Cell Biology

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