Exercise-primed extracellular vesicles improve cell-matrix adhesion and chondrocyte health

Author:

Iijima Hirotaka1ORCID,Wang Kai2ORCID,D'Amico Ella3,Tang Wan-Yee4,Rogers Renee J.5,Jakicic John M.5ORCID,Ambrosio Fabrisia6ORCID

Affiliation:

1. Institute for Advanced Research, Nagoya University, Nagoya, Japan; Biomedical and Health Informatics Unit, Graduate School of Medicine, Nagoya University, Nagoya, Japan; Department of Physical Medicine and Rehabilitation, University of Pittsburgh, Pittsburgh, PA

2. Discovery Center for Musculoskeletal Recovery, Schoen Adams Research Institute at Spaulding, Boston, MA; Department of Physical Medicine & Rehabilitation, Harvard Medical School, Boston, MA

3. Department of Physical Medicine and Rehabilitation, University of Pittsburgh, Pittsburgh, PA

4. Department of Environmental and Occupational Health, University of Pittsburgh, Pittsburgh, PA

5. Department of Internal Medicine, Division of Physical Activity and Weight Management, University of Kansas Medical Center, Kansas City, KS

6. Department of Physical Medicine and Rehabilitation, University of Pittsburgh, Pittsburgh, PA; Discovery Center for Musculoskeletal Recovery, Schoen Adams Research Institute at Spaulding, Boston, MA; Department of Physical Medicine & Rehabilitation, Harvard Medical School, Boston, MA

Abstract

Abstract Extracellular vesicles (EVs) have been suggested to transmit the health-promoting effects of exercise throughout the body. Yet, the mechanisms by which beneficial information is transmitted from extracellular vesicles to recipient cells are poorly understood, precluding a holistic understanding of how exercise promotes cellular and tissue health. In this study, using articular cartilage as a model, we introduced a network medicine paradigm to simulate how exercise facilitates communication between circulating EVs and chondrocytes, the cells resident in articular cartilage. Using the archived small RNA-seq data of EV before and after aerobic exercise, microRNA regulatory network analysis based on network propagation inferred that circulating EVs activated by aerobic exercise perturb chondrocyte-matrix interactions and downstream cellular aging processes. Building on the mechanistic framework identified through computational analyses, follow up experimental studies interrogated the direct influence of exercise on EV-mediated chondrocyte-matrix interactions. We found that pathogenic matrix signaling in chondrocytes was abrogated in the presence of exercise-primed EVs, restoring a more youthful phenotype, as determined by chondrocyte morphological profiling and evaluation of chondrogenicity. Epigenetic reprograming of the gene encoding the longevity protein, α-Klotho, mediated these effects. These studies provide mechanistic evidence that exercise transduces rejuvenation signals to circulating EVs, endowing EVs with the capacity to ameliorate cellular health even in the presence of an unfavorable microenvironmental signals.

Publisher

Research Square Platform LLC

Reference62 articles.

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1. Mechanome-guided strategies in regenerative rehabilitation;Current Opinion in Biomedical Engineering;2024-03

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