Crosstalk Between CD11b and Piezo1 Mediates Macrophage Responses to Mechanical Cues

• Published in: Frontiers in immunology Vol. 12; p. 689397
• Main Authors: Atcha, Hamza, Meli, Vijaykumar S, Davis, Chase T, Brumm, Kyle T, Anis, Sara, Chin, Jessica, Jiang, Kevin, Pathak, Medha M, Liu, Wendy F
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 22-09-2021
• Subjects: Animals; CD11b Antigen - immunology; Cell Survival; Cells, Cultured; Female; Immunology; inflammation; integrin; Ion Channels - immunology; macrophage; Macrophage Activation; Macrophages - immunology; Mechanotransduction, Cellular; Mice; Mice, Inbred C57BL; Mice, Transgenic; piezo1; stretch; stretch; macrophage; integrin; inflammation; piezo1
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2021.689397

Macrophages are versatile cells of the innate immune system that perform diverse functions by responding to dynamic changes in their microenvironment. While the effects of soluble cues, including cytokines and chemokines, have been widely studied, the effects of physical cues, including mechanical stimuli, in regulating macrophage form and function are less well understood. In this study, we examined the effects of static and cyclic uniaxial stretch on macrophage inflammatory and healing activation. We found that cyclic stretch altered macrophage morphology and responses to IFNγ/LPS and IL4/IL13. Interestingly, we found that both static and cyclic stretch suppressed IFNγ/LPS induced inflammation. In contrast, IL4/IL13 mediated healing responses were suppressed with cyclic but enhanced with static stretch conditions. Mechanistically, both static and cyclic stretch increased expression of the integrin CD11b (α
integrin), decreased expression of the mechanosensitive ion channel Piezo1, and knock down of either CD11b or Piezo1 through siRNA abrogated stretch-mediated changes in inflammatory responses. Moreover, we found that knock down of CD11b enhanced the expression of Piezo1, and conversely knock down of Piezo1 enhanced CD11b expression, suggesting the potential for crosstalk between integrins and ion channels. Finally, stretch-mediated differences in macrophage activation were also dependent on actin, since pharmacological inhibition of actin polymerization abrogated the changes in activation with stretch. Together, this study demonstrates that the physical environment synergizes with biochemical cues to regulate macrophage morphology and function, and suggests a role for CD11b and Piezo1 crosstalk in mechanotransduction in macrophages.