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Macro- and micro-scale culture environment differentially regulate the effects of crowding on macrophage function.

Authors
  • Hsu, Ssu-Chieh J1, 2
  • Luu, Thuy U1, 2
  • Smith, Tim D1, 2
  • Liu, Wendy F1, 2, 3, 4, 5
  • 1 Department of Biomedical Engineering, University of California, Irvine, California, USA.
  • 2 UCI Edwards Lifesciences Foundation Cardiovascular Innovation and Research Center, University of California, Irvine, California, USA.
  • 3 Department of Chemical and Biomolecular Engineering, University of California, Irvine, California, USA.
  • 4 Institute for Immunology, University of California, Irvine, California, USA.
  • 5 Department of Molecular Biology and Biochemistry, University of California, Irvine, California, USA.
Type
Published Article
Journal
Biotechnology and Bioengineering
Publisher
Wiley (John Wiley & Sons)
Publication Date
Jan 01, 2024
Volume
121
Issue
1
Pages
306–316
Identifiers
DOI: 10.1002/bit.28554
PMID: 37792882
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Macrophages hold vital roles in immune defense, wound healing, and tissue homeostasis, and have the exquisite ability to sense and respond to dynamically changing cues in their microenvironment. Much of our understanding of their behavior has been derived from studies performed using in vitro culture systems, in which the cell environment can be precisely controlled. Recent advances in miniaturized culture platforms also offer the ability to recapitulate some features of the in vivo environment and analyze cellular responses at the single-cell level. Since macrophages are sensitive to their surrounding environments, the specific conditions in both macro- and micro-scale cultures likely contribute to observed responses. In this study, we investigate how the presence of neighboring cells influence macrophage activation following proinflammatory stimulation in both bulk and micro-scale culture. We found that in bulk cultures, higher seeding density negatively regulated the average TNF-α secretion from individual macrophages in response to inflammatory agonists, and this effect was partially caused by the reduced cell-to-media volume ratio. In contrast, studies conducted using microwells to isolate single cells and groups of cells revealed that increasing numbers of cells positively influences their inflammatory activation, suggesting that the absolute cell numbers in the system may be important. In addition, a single inflammatory cell enhanced the inflammatory state of a small group of cells. Overall, this work helps to better understand how variations of macroscopic and microscopic culture environments influence studies in macrophage biology and provides insight into how the presence of neighboring cells and the soluble environment influences macrophage activation. © 2023 Wiley Periodicals LLC.

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