4.8 Article

Mechanically activated ion channel Piezo1 modulates macrophage polarization and stiffness sensing

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NATURE COMMUNICATIONS
卷 12, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41467-021-23482-5

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资金

  1. National Institutes of Health (NIH) National Institute of Allergy and Infectious Disease (NIAID) [R21AI128519-01, R01AI151301]
  2. National Institute of Biomedical Imaging and Bioengineering (NIBIB) [R21EB027840-01]
  3. National Institute of Arthritis, Musculoskeletal and Skin Diseases (NIAMS) [R21AR077288]
  4. National Institute of Neurological Disorders and Stroke (NINDS) [R01NS14609]
  5. NIH Director's Fund [DP2AT010376]
  6. NINDS [R01NS109810]
  7. NIH National Institute [5T32 HL116270-3]
  8. American Heart Association Pre-Doctoral Fellowship [20PRE35200220]
  9. HHMI Gilliam Fellowship for Advanced Study [GT11549]
  10. UC Irvine Medical Scientist Training Program NIH [T32 GM008620-18]
  11. NIH NIAID [AI142988-01A1]
  12. Cancer Center Support Grant [CA-62203]
  13. Center for Complex Biological Systems Support Grant at the University of California, Irvine [GM-076516]
  14. NIAID [R01AI121945]
  15. [1S10OD025064-01A1]

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Studies reveal that Piezo1 serves as a mechanosensor of stiffness in macrophages, influencing their polarization responses.
Macrophages perform diverse functions within tissues during immune responses to pathogens and injury, but molecular mechanisms by which physical properties of the tissue regulate macrophage behavior are less well understood. Here, we examine the role of the mechanically activated cation channel Piezo1 in macrophage polarization and sensing of microenvironmental stiffness. We show that macrophages lacking Piezo1 exhibit reduced inflammation and enhanced wound healing responses. Additionally, macrophages expressing the transgenic Ca2+ reporter, Salsa6f, reveal that Ca2+ influx is dependent on Piezo1, modulated by soluble signals, and enhanced on stiff substrates. Furthermore, stiffness-dependent changes in macrophage function, both in vitro and in response to subcutaneous implantation of biomaterials in vivo, require Piezo1. Finally, we show that positive feedback between Piezo1 and actin drives macrophage activation. Together, our studies reveal that Piezo1 is a mechanosensor of stiffness in macrophages, and that its activity modulates polarization responses. Macrophages perform diverse functions during immune responses, but the molecular mechanisms by which physical properties of the tissue regulate macrophage behavior remain unknown. Here the authors find that Piezo1 is a mechanosensor of stiffness, and that its activity modulates macrophage polarization responses.

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