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INFORMATION FOR

    P. Kent Langston, PhD

    Assistant Professor
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    Assistant Professor

    Biography

    Dr. Kent Langston is an assistant professor of Pathology at Yale School of Medicine and a member of the Yale Center for Research on Aging (Y-Age). He received his Ph.D. from Harvard University for his work in Dr. Tiffany Horng's laboratory on metabolic regulation of macrophage activation and tolerance. He completed his postdoctoral training with Drs. Diane Mathis and Christophe Benoist in the Department of Immunology at Harvard Medical School. In the Mathis-Benoist laboratory, Dr. Langston integrated his personal interest in exercise with his scientific interests in cellular immunology and metabolic biology to investigate how the immune system responds to exercise and regulates its beneficial effects, particularly in skeletal muscle. His work 1) elucidated the dynamics of physiological inflammatory responses to endurance exercise in skeletal muscles, 2) demonstrated that appropriate regulation of such inflammation is required for the muscle-specific and organism-level metabolic adaptations and improved performance typical of training, 3) revealed that inflammatory responses to exercise are initiated by mechanical stress-induced activation of muscle mesenchymal stromal cells.

    The Langston laboratory is further defining the cellular and molecular features of exercise-induced inflammatory responses in youth and during aging – an endeavor that is partly supported by an NIA/NIH K22 award – with an emphasis on elucidating how non-parenchymal cells sense exercise and regulate its benefits. An ultimate goal of this work is to design exercise-inspired interventions to combat modern afflictions associated with chronic inflammation, improve regeneration and performance after injury, reduce the pathology of musculoskeletal diseases, and combat age-related frailty (i.e., increase healthspan).

    Last Updated on March 11, 2026.

    Appointments

    Education & Training

    Postdoctoral Fellow
    Harvard Medical School (2025)
    PhD
    Harvard University, Immunometabolism (2019)
    BS (Hon)
    Wake Forest University, Chemistry (2014)

    Research

    Overview

    Using a multimodal experimental approach, we demonstrated that appropriate regulation of physiological inflammation by regulatory T cells (Tregs) is required for the muscle-specific and organism-level metabolic adaptations and improved performance typical of exercise training (Langston et al. 2023. Science Immunology). Notably, this was the first study in which an immunocyte subset was punctually ablated to assess its importance in exercise adaptation. We identified interferon gamma as a T-cell and NK-cell effector molecule that is unleashed in Treg-deficient mice and is necessary and sufficient to impair muscle mitochondrial function to the detriment of endurance-exercise performance. The profound defects in exercise adaptation, at the muscle level and systemically, caused by excessive inflammatory responses prompted us to ask why exercise induces muscle inflammation at all – i.e., how non-parenchymal cells in muscle sense exercise. Interestingly, we found that muscle mesenchymal stromal cells (MmSCs), also commonly called fibroadipogenic progenitors, sense exercise-induced changes in the mechanical properties of muscle via the mechanosensitive ion channel Piezo1 (Langston et al. 2026. Nature Immunology). Such mechanosensation triggers an inflammatory reaction among MmSCs, which is characterized by their upregulation of many immunomodulatory factors, including IL-6 and CCL2. Notably, this response was site-specific, occurring only in muscles that exhibited changes in stiffness in response to exercise (i.e., gastrocnemius and quadriceps, not tibialis anterior), and was necessary for consequent recruitment of leukocytes to muscle. A similar reaction also occurs in injured and aged muscles, nominating mechanosensing as a potential target for anti-inflammatory therapies for these conditions.


    The Langston laboratory aims to characterize the immunometabolic drivers of exercise adaptation and muscle aging. We are a growing interdisciplinary team that values creativity and collaboration. If you are interested in muscle immunobiology and/or bioengineering, please do not hesitate to reach out.

    Medical Research Interests

    Aging; Exercise; Fibrosis; Immunity, Cellular; Inflammation; Mitochondria; Musculoskeletal System

    Research at a Glance

    Publications Timeline

    A big-picture view of P. Kent Langston's research output by year.

    Publications

    Featured Publications

    2026

    2025

    2023

    Academic Achievements & Community Involvement

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