4.8 Article

The mechanosensitive ion channel PIEZO1 is expressed in tendons and regulates physical performance

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SCIENCE TRANSLATIONAL MEDICINE
卷 14, 期 647, 页码 -

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scitranslmed.abj5557

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资金

  1. AMED-CREST from AMED (Japan Agency for Medical Research and Development) [JP20gm0810008]
  2. JSPS KAKENHI [19KK0227, 20H05696]
  3. NIH [AR050631, AR065379]
  4. Grants-in-Aid for Scientific Research [20H05696, 19KK0227] Funding Source: KAKEN

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This study reveals how mechanical stress affects physical performance by regulating PIEZO1 in tendons. The researchers found that tendon-specific knock-in mice with the gain-of-function variant R2482H Piezo1 had higher jumping abilities and faster running speeds due to enhanced tendon anabolism and increased expression of tendon-specific transcription factors. This finding suggests that PIEZO1 could be a potential target for enhancing physical performance.
How mechanical stress affects physical performance via tendons is not fully understood. Piezo1 is a mechanosensitive ion channel, and E756del PIEZO1 was recently found as a gain-of-function variant that is common in individuals of African descent. We generated tendon-specific knock-in mice using R2482H Piezo1, a mouse gain-of-function variant, and found that they had higher jumping abilities and faster running speeds than wild-type or muscle-specific knock-in mice. These phenotypes were associated with enhanced tendon anabolism via an increase in tendon-specific transcription factors, Mohawk and Scleraxis, but there was no evidence of changes in muscle. Biomechanical analysis showed that the tendons of R2482H Piezo1 mice were more compliant and stored more elastic energy, consistent with the enhancement of jumping ability. These phenotypes were replicated in mice with tendon-specific R2482H Piezo1 replacement after tendon maturation, indicating that PIEZO1 could be a target for promoting physical performance by enhancing function in mature tendon. The frequency of E756del PIEZO1 was higher in sprinters than in population-matched nonathletic controls in a small Jamaican cohort, suggesting a similar function in humans. Together, this human and mouse genetic and physiological evidence revealed a critical function of tendons in physical performance, which is tightly and robustly regulated by PIEZO1 in tenocytes.

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