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Compliant Substrates Enhance Macrophage Cytokine Release and NLRP3 Inflammasome Formation During Their Pro-Inflammatory Response

  • Immune cells process a myriad of biochemical signals but their function and behavior are also determined by mechanical cues. Macrophages are no exception to this. Being present in all types of tissues, macrophages are exposed to environments of varying stiffness, which can be further altered under pathological conditions. While it is becoming increasingly clear that macrophages are mechanosensitive, it remains poorly understood how mechanical cues modulate their inflammatory response. Here we report that substrate stiffness influences the expression of pro-inflammatory genes and the formation of the NLRP3 inflammasome, leading to changes in the secreted protein levels of the cytokines IL-1β and IL-6. Using polyacrylamide hydrogels of tunable elastic moduli between 0.2 and 33.1 kPa, we found that bone marrow-derived macrophages adopted a less spread and rounder morphology on compliant compared to stiff substrates. Upon LPS priming, the expression levels of the gene encoding for TNF-α were higher on more compliant hydrogels. When additionally stimulating macrophages with the ionophore nigericin, we observed an enhanced formation of the NLRP3 inflammasome, increased levels of cell death, and higher secreted protein levels of IL-1β and IL-6 on compliant substrates. The upregulation of inflammasome formation on compliant substrates was not primarily attributed to the decreased cell spreading, since spatially confining cells on micropatterns led to a reduction of inflammasome-positive cells compared to well-spread cells. Finally, interfering with actomyosin contractility diminished the differences in inflammasome formation between compliant and stiff substrates. In summary, we show that substrate stiffness modulates the pro-inflammatory response of macrophages, that the NLRP3 inflammasome is one of the components affected by macrophage mechanosensing, and a role for actomyosin contractility in this mechanosensory response. Thus, our results contribute to a better understanding of how microenvironment stiffness affects macrophage behavior, which might be relevant in diseases where tissue stiffness is altered and might potentially provide a basis for new strategies to modulate inflammatory responses.

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Metadaten
Document Type:Article
Author:Joan-Carles EscolanoORCiD, Anna V. TaubenbergerORCiD, Shada AbuhattumORCiD, Christine Schweitzer, Aleeza FarrukhORCiD, Aránzazu del Campo BécaresORCiD, Clare E. BryantORCiD, Jochen GuckORCiD
URN:urn:nbn:de:bsz:291:415-1278
DOI:https://doi.org/10.3389/fcell.2021.639815
Parent Title (English):Frontiers in Cell and Developmental Biology
Volume:9
First Page:682
Language:English
Year of first Publication:2021
Release Date:2022/08/18
Tag:Innate immunity; Macrophages; Mechanosensing; NLRP3 inflammasome; Substrate stiffness
Impact:06.081 (2021)
Funding Information:EU’s Horizon 2020 Research and Innovation Program under the Marie Skłodowska-Curie Grant Agreement No. 641639 (ITN Biopol); Wellcome Trust Investigator Award 108045/Z/15/Z; German Cancer Aid (Deutsche Krebshilfe).
Scientific Units:Dynamical Biomaterials
DDC classes:500 Naturwissenschaften und Mathematik / 570 Biowissenschaften, Biologie
Open Access:Open Access
Signature:INM 2021/046
Licence (German):License LogoCreative Commons - CC BY - Namensnennung 4.0 International