Metabolic Regulation of Tendon Inflammation and Healing Following Injury
- PMID: 33569739
- PMCID: PMC7983167
- DOI: 10.1007/s11926-021-00981-4
Metabolic Regulation of Tendon Inflammation and Healing Following Injury
Abstract
Purpose of review: This review seeks to provide an overview of the role of inflammation and metabolism in tendon cell function, tendinopathy, and tendon healing. We have summarized the state of knowledge in both tendon and enthesis.
Recent findings: Recent advances in the field include a substantial improvement in our understanding of tendon cell biology, including the heterogeneity of the tenocyte environment during homeostasis, the diversity of the cellular milieu during in vivo tendon healing, and the effects of inflammation and altered metabolism on tendon cell function in vitro. In addition, the mechanisms by which altered systemic metabolism, such as diabetes, disrupts tendon homeostasis continue to be better understood. A central conclusion of this review is the critical need to better define fundamental cellular and signaling mechanisms of inflammation and metabolism during tendon homeostasis, tendinopathy, and tendon healing in order to identify therapies to enhance or maintain tendon function.
Keywords: Enthesis; Inflammation; Metabolism; Tendinopathy; Tendon; Tendon healing.
Conflict of interest statement
Conflict of Interest
Jessica Ackerman, Katherine Best, Samantha Muscat and Alayna Loiselle declare that they have no conflicts of interest.
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References
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Izumi S, Otsuru S, Adachi N, Akabudike N, Enomoto-Iwamoto M. Control of glucose metabolism is important in tenogenic differentiation of progenitors derived from human injured tendons. PloS one. 2019;14(3):e0213912.
* This study examines how metabolic flux through glycolysis and the TCA cycle differently influence differentiation potential of cells derived from human injured tendons.
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Zhang K, Asai S, Yu B, Enomoto-Iwamoto M. IL-1β irreversibly inhibits tenogenic differentiation and alters metabolism in injured tendon-derived progenitor cells in vitro. Biochem Biophys Res Commun 2015;463(4):667–72.
* This study demonstrated that pro-inflammatory cytokine IL-1β enhanced lactate production, directly affecting expression of tendon marker Scx and matrix gene Col1.
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