Isolation and culture of murine bone marrow-derived macrophages for nitric oxide and redox biology

Jade D. Bailey, Andrew Shaw, Eileen McNeill, Thomas Nicol, Marina Diotallevi, Surawee Chuaiphichai, Jyoti Patel, Ashley Hale, Keith Michael Channon, Mark J. Crabtree*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Citations (Scopus)

Abstract

Macrophages are mononuclear phagocytes derived from haematopoietic progenitors that are widely distributed throughout the body. These cells participate in both innate and adaptive immune responses and lie central to the processes of inflammation, development, and homeostasis. Macrophage physiology varies depending on the environment in which they reside and they exhibit rapid functional adaption in response to external stimuli. To study macrophages in vitro, cells are typically cultured ex vivo from the peritoneum or alveoli, or differentiated from myeloid bone marrow progenitor cells to form bone marrow-derived macrophages (BMDMs). BMDMs represent an efficient and cost-effective means of studying macrophage biology. However, the inherent sensitivity of macrophages to biochemical stimuli (such as cytokines, metabolic intermediates, and RNS/ROS) makes it imperative to control experimental conditions rigorously. Therefore, the aim of this study was to establish an optimised and standardised method for the isolation and culture of BMDMs. We used classically activated macrophages isolated from WT and nitric oxide (NO)-deficient mice to develop a standardised culture method, whereby the constituents of the culture media are defined. We then methodically compared our standardised protocol to the most commonly used method of BMDM culture to establish an optimal protocol for the study of nitric oxide (NO)-redox biology and immunometabolism in vitro.
Original languageEnglish
Pages (from-to)17-29
Number of pages13
JournalNitric Oxide
Volume100-101
DOIs
Publication statusPublished - 1 Aug 2020

Keywords

  • Macrophage
  • MCSF
  • Tetrahydrobiopterin
  • Nitric oxide

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